Itoh Hideki 伊藤英樹

… Alternative Names

ITOH Hideki 伊藤英樹

Less

Researcher Number	30402738
Other IDs
External Links
Affiliation (Current)	2025: 広島大学, 病院(医), 教授
Affiliation (based on the past Project Information) *help	2019 – 2023: 広島大学, 病院(医), 教授 2017 – 2018: 滋賀医科大学, 医学部, 准教授 2017: 滋賀医科大学, 医学部, 助教 2016: 滋賀医科大学, 医学部, 講師 2007 – 2015: Shiga University of Medical Science, 医学部, 助教 2011: 滋賀医科大学, 医学, 助教 2006: 滋賀医科大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Circulatory organs internal medicine / Basic Section 53020:Cardiology-related / Cardiovascular medicine / Human genetics / Complex systems Except Principal Investigator Circulatory organs internal medicine / Cardiovascular medicine
Keywords	Principal Investigator 遺伝子 / QT延長症候群 / 突然死 / チャネル / シミュレーション / イオンチャネル / 変異 / 薬剤 / 後天性 / SCN5A … More / 不整脈 / ブルガダ症候群 / 筋小胞体 / 特発性心室細動 / リアノジン / 小胞体 / カルシウム / 心室細動 / リアノジン受容体 / 多型 / 薬剤性 / QT延長 / 個別化医療 / 機能 / メンデル遺伝 / KCNQ1 / 筋緊張性ジストロフィー / 先天性 / HERG / 遺伝子異常 / KCNH2 / Brugada症候群 … More Except Principal Investigator 遺伝子 / 機能解析 / 遺伝性不整脈 / ブルガダ症候群 / SCN5A / コピー数変動 / 循環器・高血圧 / 遺伝学 / 高血圧 / 循環器 / テーラーメイド医療 / iPS細胞 / 遺伝子解析 / コンピュータシミュレーション / パッチクランプ法 / 分子心臓病態学 / カテーテル治療 / ホームモニタリング / 評価法 / 再発 / カテーテルアブレーション / 心房細動 / イオンチャネル / 蛋白質 / 生理学 Less

The genetic analysis and underlying function of the endoplasmic reticulum membrane protein targeting inherited arrhythmogenic syndromesPrincipal Investigator
- Principal Investigator
  
  Itoh Hideki
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Hiroshima University
The risk stratification of drug-induced long QT syndrome upon the underlying geneticsPrincipal Investigator
- Principal Investigator
  
  Itoh Hideki
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Hiroshima University
  Shiga University of Medical Science
Multilateral Research on the Mechanisms of Inherited Arrhythmias
- Principal Investigator
  
  Horie Minoru
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Shiga University of Medical Science
心筋イオンチャネル病のリスク層別化と臨床管理におけるシミュレーションの応用Principal Investigator
- Principal Investigator
  
  伊藤英樹
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
- Review Section
  
  Complex systems
- Research Institution
  Shiga University of Medical Science
Genetic epidemiology in the ion channel diseasePrincipal Investigator
- Principal Investigator
  
  Itoh Hideki
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Shiga University of Medical Science
Multidisciplinary Studies on Molecular Pathogenesis of Inherited Primary Arrhythmia Syndromes
- Principal Investigator
  
  HORIE Minoru
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Shiga University of Medical Science
Evaluation of Efficacy and Long-term Results of Catheter Ablation in Drug-refractory Atrial Fibrillation
- Principal Investigator
  
  ITO Makoto
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Shiga University of Medical Science
潜在性突然死症候群の顕在化に関与する遺伝的背景と分子病態の解明Principal Investigator
- Principal Investigator
  
  伊藤英樹
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Shiga University of Medical Science
Genotype-phenotype relation study on inherited cardiac arrhythmias as ion hcannel diseases
- Principal Investigator
  
  HORIE Minoru
- Project Period (FY)
  2007 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Shiga University of Medical Science
Genetic Backgrounds and Functional Analysis in SCN5A Mutation-Negative Brugada SyndromePrincipal Investigator
- Principal Investigator
  
  ITOH Hideki
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Shiga University of Medical Science

[Book] Management of Cardiac Arrhythmias, 3rd ed. Chapter 20 Acquired Long QT Syndrome and Torsades de Pointes2020
- Author(s)
  Itoh H, Shimizu W
- Publisher
  Springer Nature
- Data Source
  KAKENHI-PROJECT-17K09494
[Book] Management of Cardiac Arrhythmias,3rd ed.2020
- Author(s)
  Yan GX, Kowey PR, Antzelevitch C (Eds.) Itoh H, Shimizu W (Chap20)
- Total Pages
  876
- Publisher
  Springer Nature
- Data Source
  KAKENHI-PROJECT-20K08473
[Book] 不整脈薬物治療ガイドライン2020年改訂版2020
- Author(s)
  小野克重、岩﨑雄樹、清水渉、伊藤英樹、他
- Total Pages
  154
- Publisher
  日本循環器学会/日本不整脈心電学会合同ガイドライン
- Data Source
  KAKENHI-PROJECT-17K09494
[Book] 循環器疾患最新の治療2018-20192018
- Author(s)
  永井　良三、伊藤　浩、山下　武志
- Total Pages
  540
- Publisher
  南江堂
- ISBN
  9784524252183
- Data Source
  KAKENHI-PROJECT-15H04818
[Book] Myotonic Dystrophy2018
- Author(s)
  Hideki Itoh, et al.
- Total Pages
  214
- Publisher
  Springer Nature
- Data Source
  KAKENHI-PROJECT-17K09494
[Book] 不整脈症候群2015
- Author(s)
  伊藤英樹、他
- Total Pages
  196
- Publisher
  南江堂
- Data Source
  KAKENHI-PUBLICLY-25136705
[Book] 不整脈治療update2015
- Author(s)
  伊藤英樹、藤居祐介、堀江　稔
- Total Pages
  224
- Publisher
  医薬ジャーナル社
- Data Source
  KAKENHI-PROJECT-15H04818
[Book] Electrocardiography A to Z-心電図のリズムと波を見極める.2015
- Author(s)
  伊藤英樹、他
- Total Pages
  299
- Publisher
  日本医師会雑誌特別号
- Data Source
  KAKENHI-PROJECT-25460406
[Book] 不整脈症候群2015
- Author(s)
  伊藤英樹、他
- Total Pages
  204
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-25460406
[Book] 見逃すな！薬物中毒と電解質異常. レジデントノート　心電図の読み方トレニーング2013
- Author(s)
  伊藤英樹
- Publisher
  羊土社
- Data Source
  KAKENHI-PUBLICLY-25136705
[Book] 見逃すな！薬物中毒と電解質異常. レジデントノート　心電図の読み方トレニーング2013
- Author(s)
  伊藤英樹
- Publisher
  羊土社
- Data Source
  KAKENHI-PROJECT-25460406
[Book] 今さら聞けない心電図2010
- Author(s)
  池田隆徳、伊藤英樹, 他
- Total Pages
  294
- Publisher
  MEDICAL VIEW
- Data Source
  KAKENHI-PROJECT-21790718
[Book] 致死性不整脈の遺伝子診断.Annual Review循環器20072007
- Author(s)
  伊藤英樹,堀江稔
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-19390212
[Book] Annual Review循環器20072007
- Author(s)
  伊藤英樹
- Total Pages
  312
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-18790496
[Book] QT間隔の診かた・考え方2007
- Author(s)
  伊藤英樹, 他
- Total Pages
  260
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-18790496
[Book] Annual Review 20072007
- Author(s)
  伊藤英樹, 他.
- Total Pages
  312
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-18790496
[Book] QT間隔の診かた・考え方2007
- Author(s)
  伊藤英樹
- Total Pages
  260
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-18790496
[Book] Annual Review循環器2007
- Author(s)
  伊藤英樹
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] Experience-based treatment strategy for cardiomyopathy of Duchenne muscular dystrophy2024
- Author(s)
  Kimura K, Morita H, Nakanishi K, Daimon M, Nakamura A, Matsumura T, Takeda A, Itoh H, Okada T, Takeda N
- Journal Title
  
  Neurological Therapeutics
  
  Volume: -
- Data Source
  KAKENHI-PROJECT-20K08473
[Journal Article] Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants2024
- Author(s)
  Kashiwa A, Itoh H, Makiyama T, Wada Y, Ozawa J, Kato K, Fukuyama M, Nakajima T, Ohno S, Horie M.
- Journal Title
  
  Heart Rhythm
  
  Volume: In press Issue: 7 Pages: 1113-1120
- DOI
  10.1016/j.hrthm.2024.02.021
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-23K06845, KAKENHI-PROJECT-23K07528, KAKENHI-PROJECT-20K08473
[Journal Article] One Year Treatment Results in Japanese National Hospitals2024
- Author(s)
  Kimura K, Wakisaka A, Morita H, Nakanishi K, Daimon M, Nojima M, Itoh H, Takeda A, Kitao R, Imai T, Ikeda T, Nakajima T, Watanabe C, Furukawa T, Ohno I, Ishida C, Takeda N, Komai K
- Journal Title
  
  Int. Heart J.
  
  Volume: 65 Issue: 2 Pages: 211-217
- DOI
  10.1536/ihj.23-563
- ISSN
  1349-2365, 1349-3299
- Year and Date
  2024-03-30
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K06905, KAKENHI-PROJECT-20K08473
[Journal Article] Novel CACNA1C R511Q mutation, located in domain Ⅰ-Ⅱ linker, causes non-syndromic type-8 long QT syndrome2022
- Author(s)
  Nakajima Tadashi、Kawabata-Iwakawa Reika、Tamura Shuntaro、Hasegawa Hiroshi、Kobari Takashi、Itoh Hideki、Horie Minoru、Nishiyama Masahiko、Kurabayashi Masahiko、Kaneko Yoshiaki、Ishii Hideki
- Journal Title
  
  PLOS ONE
  
  Volume: 17 Issue: 7 Pages: e0271796-e0271796
- DOI
  10.1371/journal.pone.0271796
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-21K08022, KAKENHI-PROJECT-20K08487
[Journal Article] JCS/JHRS 2020 Guideline on Pharmacotherapy of Cardiac Arrhythmias2022
- Author(s)
  Ono K, Iwasaki YK, Akao M, Makiyama T, Maruyama M, Miake J, Muraji S, Murata H, Morita N, Yokoshiki H, Yoshioka K, Yodogawa K, Inoue H, Okumura K, Kimura T, Tsutsui H, Shimizu W
- Journal Title
  
  Circ J
  
  Volume: 86 Issue: 11 Pages: 1790-1924
- DOI
  10.1253/circj.CJ-20-1212
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2022-10-25
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-19K08566, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-20K20662
[Journal Article] Novel CALM3 Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation Family2022
- Author(s)
  Kato Koichi、Isbell Holly M.、Fressart Veronique、Denjoy Isabelle、Debbiche Amal、Itoh Hideki、Poinsot Jacques、George Alfred L.、Coulombe Alain、Shea Madeline A.、Guicheney Pascale
- Journal Title
  
  Circulation: Arrhythmia and Electrophysiology
  
  Volume: 15 Issue: 3
- DOI
  10.1161/circep.121.010572
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-20K17113
[Journal Article] Differences in Pharmaceutical Intervention Triggers for the Optimization of Medication by Patient Age: A University Hospital Study2021
- Author(s)
  Shibata Yuuka、Itoh Hideki、Matsuo Hiroaki、Nakajima Kazue
- Journal Title
  
  Biological and Pharmaceutical Bulletin
  
  Volume: 44 Issue: 8 Pages: 1060-1066
- DOI
  10.1248/bpb.b21-00143
- NAID
  130008070531
- ISSN
  0918-6158, 1347-5215
- Year and Date
  2021-08-01
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08473
[Journal Article] Sudden death after inappropriate shocks of implantable cardioverter defibrillator in a catecholaminergic polymorphic ventricular tachycardia case with a novel RyR2 mutation2021
- Author(s)
  Itoh Hideki、Murayama Takashi、Kurebayashi Nagomi、Ohno Seiko、Kobayashi Takuya、Fujii Yusuke、Watanabe Masaya、Ogawa Haruo、Anzai Toshihisa、Horie Minoru
- Journal Title
  
  Journal of Electrocardiology
  
  Volume: 69 Pages: 111-118
- DOI
  10.1016/j.jelectrocard.2021.09.015
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K07105, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-19H03404, KAKENHI-PROJECT-21H02411
[Journal Article] High incidence of major bleeding with off-label use of edoxaban2021
- Author(s)
  Fukui Rika、Hira Daiki、Kunitsu Yuki、Isono Tetsuichiro、Tabuchi Yohei、Ikuno Yoshihiro、Ueshima Satoshi、Itoh Hideki、Tanaka Toshihiro、Terada Tomohiro
- Journal Title
  
  Journal of Clinical Biochemistry and Nutrition
  
  Volume: 69 Issue: 3 Pages: 311-316
- DOI
  10.3164/jcbn.21-9
- NAID
  130008110266
- ISSN
  0912-0009, 1880-5086
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-21K06665
[Journal Article] Cardiac conduction disorders as markers of cardiac events in myotonic dystrophy type 1.2020
- Author(s)
  2.Itoh H, Hisamatsu T, Tamura T, Segawa K, Takahashi T, Takada H, Kuru S, Wada C, Suzuki M, Suwazono S, Sasaki S, Okumura K, Horie M, Takahashi MP, Matumura T.
- Journal Title
  
  J Am Heart Assoc.
  
  Volume: 9 Issue: 17
- DOI
  10.1161/jaha.119.015709
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K07992, KAKENHI-PROJECT-20K08473
[Journal Article] 遺伝性不整脈疾患における筋小胞体Caシグナリング2020
- Author(s)
  伊藤英樹、堀江　稔、竹島　浩
- Journal Title
  
  Bio Clinica
  
  Volume: 35 Pages: 76-79
- Data Source
  KAKENHI-PROJECT-20K08473
[Journal Article] Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome2020
- Author(s)
  Lahrouchi N, Tadros R, Crotti L, Makiyama T et al.
- Journal Title
  
  Circulation
  
  Volume: 142 Issue: 4 Pages: 324-338
- DOI
  10.1161/circulationaha.120.045956
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416
[Journal Article] Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls2020
- Author(s)
  2.Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, et al.
- Journal Title
  
  Genetics in Medicine
  
  Volume: 23 Issue: 1 Pages: 47-58
- DOI
  10.1038/s41436-020-00946-5
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08100, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18K15407, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-20K08416
[Journal Article] Clinical Care Recommendations for Cardiologists Treating Adults With Myotonic Dystrophy2020
- Author(s)
  McNally Elizabeth M.、Mann Douglas L.、Pinto Yigal、Bhakta Deepak、Tomaselli Gordon、Nazarian Saman、Groh William J.、Tamura Takuhisa、Duboc Denis、Itoh Hideki、Hellerstein Leah、Mammen Pradeep P. A.
- Journal Title
  
  Journal of the American Heart Association
  
  Volume: 9 Issue: 4
- DOI
  10.1161/jaha.119.014006
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09494
[Journal Article] 後天性QT延長症候群の遺伝的背景2019
- Author(s)
  伊藤英樹
- Journal Title
  
  心電図
  
  Volume: 39 Pages: 5-15
- NAID
  130007630118
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09494
[Journal Article] Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients2019
- Author(s)
  Shimizu Wataru、Makimoto Hisaki、Yamagata Kenichiro、Kamakura Tsukasa、Wada Mitsuru、Miyamoto Koji、Inoue-Yamada Yuko、Okamura Hideo、Ishibashi Kohei、Noda Takashi、Nagase Satoshi、Miyazaki Aya、Sakaguchi Heima、Shiraishi Isao、Makiyama Takeru、Ohno Seiko、Itoh Hideki、et al
- Journal Title
  
  JAMA Cardiology
  
  Volume: in press Issue: 3 Pages: 246-254
- DOI
  10.1001/jamacardio.2018.4925
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-18K08100, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15KK0302, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-17K09524, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08075, KAKENHI-PROJECT-19K08566, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18H02808
[Journal Article] Population pharmacokinetics and pharmacodynamics of apixaban linking its plasma concentration to intrinsic activated coagulation factor X activity in Japanese patients with atrial fibrillation2019
- Author(s)
  Ueshima Satoshi、Hira Daiki、Tomitsuka Chiho、Nomura Miki、Kimura Yuuma、Yamane Takuya、Tabuchi Yohei、Ozawa Tomoya、Itoh Hideki、Horie Minoru、Terada Tomohiro、Katsura Toshiya
- Journal Title
  
  The AAPS Journal
  
  Volume: 21 Issue: 5 Pages: 80-80
- DOI
  10.1208/s12248-019-0353-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K06766, KAKENHI-PROJECT-18K06782, KAKENHI-PROJECT-19K07234, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-17K15504
[Journal Article] 遺伝性不整脈の診療に関するガイドライン2017年改訂版2018
- Author(s)
  Itoh Hideki, et al
- Journal Title
  
  Circ J
  
  Volume: - Pages: 1-79
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09494
[Journal Article] Population pharmacokinetics and pharmacogenomics of apixaban in Japanese adult patients with atrial fibrillation.2018
- Author(s)
  Ueshima S, Hira D, Kimura Y, Fujii R, Tomitsuka C, Yamane T, Tabuchi Y, Ozawa T, Itoh H, Ohno S, Horie M, Terada T, Katsura T.
- Journal Title
  
  Br. J. Clin. Pharmacol.
  
  Volume: - Issue: 6 Pages: 1301-1312
- DOI
  10.1111/bcp.13561
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K15504, KAKENHI-PROJECT-17K15528, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K06766, KAKENHI-PROJECT-18K06782, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-15K08114
[Journal Article] Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations2018
- Author(s)
 Miyata Kazuaki、Ohno Seiko、Itoh Hideki、Horie Minoru
- Journal Title
 
 Intern. Med.
 
 Volume: 57 Issue: 13 Pages: 1813-1817
- DOI
 10.2169/internalmedicine.9843-17
- NAID
 130007387124
- ISSN
 0918-2918, 1349-7235
- Year and Date
 2018-07-01
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-18K07875
[Journal Article] A challenge for mutation specific risk stratification in long QT syndrome type 12018
- Author(s)
  Yagi Noriaki、Itoh Hideki、Hisamatsu Takashi、Tomita Yukinori、Kimura Hiromi、Fujii Yusuke、Makiyama Takeru、Horie Minoru、Ohno Seiko
- Journal Title
  
  Journal of Cardiology
  
  Volume: 18 Issue: 1 Pages: 30012-1
- DOI
  10.1016/j.jjcc.2017.12.011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-18K07875
[Journal Article] A hERG mutation E1039X produced a synergistic lesion on IKs together with KCNQ1-R174C mutation in a LQTS family with three compound mutations2018
- Author(s)
  Wu Jie、Mizusawa Yuka、Ohno Seiko、Ding Wei-Guang、Higaki Takashi、Wang Qi、Kohjitani Hirohiko、Makiyama Takeru、Itoh Hideki、Toyoda Futoshi、James Andrew F.、Hancox Jules C.、Matsuura Hiroshi、Horie Minoru
- Journal Title
  
  Scientific Reports
  
  Volume: 8 Issue: 1 Pages: 3129-3129
- DOI
  10.1038/s41598-018-21442-6
- NAID
  120006529715
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-18K07875
[Journal Article] Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome2018
- Author(s)
  Fukumoto Daisuke、Ding Wei-Guang、Wada Yuko、Fujii Yusuke、Ichikawa Mari、Takayama Koichiro、Fukuyama Megumi、Kato Koichi、Itoh Hideki、Makiyama Takeru、Omatsu-Kanbe Mariko、Matsuura Hiroshi、Horie Minoru、Ohno Seiko
- Journal Title
  
  Journal of Cardiology
  
  Volume: 71 Issue: 4 Pages: 401-408
- DOI
  10.1016/j.jjcc.2017.10.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-17K15999
[Journal Article] 疾患・病態別にみた医薬品の禁忌　循環器疾患2017
- Author(s)
  伊藤英樹
- Journal Title
  
  月刊薬事
  
  Volume: 印刷中
- Data Source
  KAKENHI-PROJECT-25460406
[Journal Article] Drug-induced fatal arrhythmias: Acquired long QT and Brugada syndromes2017
- Author(s)
  Turker Isik、Ai Tomohiko、Itoh Hideki、Horie Minoru
- Journal Title
  
  Pharmacol Ther
  
  Volume: 176 Pages: 48-59
- DOI
  10.1016/j.pharmthera.2017.05.001
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04818
[Journal Article] Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote.2017
- Author(s)
  Fujii Y, Horie M, et al.
- Journal Title
  
  J Cardiol
  
  Volume: 印刷中 Issue: 1 Pages: 74-79
- DOI
  10.1016/j.jjcc.2016.09.010
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-17K09495
[Journal Article] Drug-induced Brugada-type Electrocardiogram: A Cause of Sudden Death in Patients with Schizophrenia?2017
- Author(s)
  Itoh Hideki
- Journal Title
  
  Intern. Med.
  
  Volume: 56 Issue: 22 Pages: 2969-2970
- DOI
  10.2169/internalmedicine.9087-17
- NAID
  130006201574
- ISSN
  0918-2918, 1349-7235
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09494
[Journal Article] Impact of ABCB1, ABCG2, and CYP3A5 polymorphisms on plasma trough concentrations of apixaban in Japanese patients with atrial fibrillation2017
- Author(s)
  Satoshi Ueshima, Daiki Hira, Ryo Fujii, Yuuma Kimura, Chiho Tomitsuka, Takuya Yamane, Yohei Tabuchi, Tomoya Ozawa, Hideki Itoh, Minoru Horie, Tomohiro Terada, Toshiya Katsura
- Journal Title
  
  Pharmacogenetics and Genomics
  
  Volume: 27 Issue: 9 Pages: 329-336
- DOI
  10.1097/fpc.0000000000000294
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K08114, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-17K15504, KAKENHI-PROJECT-17K15528, KAKENHI-PROJECT-15H04818
[Journal Article] Arrhtyhmia risk and β-blocker therapy in pregnant women with long QT syndrome.2017
- Author(s)
  Ishibashi K, Horie M, et al.
- Journal Title
  
  Heart
  
  Volume: 印刷中 Issue: 17 Pages: 0-0
- DOI
  10.1136/heartjnl-2016-310617
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-26461130, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-17K09495
[Journal Article] Splicing misregulation of SCN5A contributes to　cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.2016
- Author(s)
  Freyermuth F, Rau F, Kokunai Y, Linke T, Sellier C, Nakamori M, Kino Y,.......Zimmer T, Furling D, Takahashi MP, Charlet-Berguerand N.
- Journal Title
  
  Nat Commun.
  
  Volume: 7 Issue: 1 Pages: 11067-11067
- DOI
  10.1038/ncomms11067
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09314, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25461053, KAKENHI-PROJECT-15K15339, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25461106, KAKENHI-PROJECT-25253066, KAKENHI-PROJECT-25713034, KAKENHI-PUBLICLY-15H01567, KAKENHI-PUBLICLY-16H01345, KAKENHI-PROJECT-15H01801, KAKENHI-PROJECT-16H05238, KAKENHI-PROJECT-15K15342, KAKENHI-PROJECT-16K09431
[Journal Article] The genetics underlying acquired long QT syndrome: impact for genetic screening.2016
- Author(s)
  Itoh H, Crotti L, Aiba T, Spazzolini C, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M.
- Journal Title
  
  European Heart Journal
  
  Volume: 37 (18) Issue: 18 Pages: 1456-1464
- DOI
  10.1093/eurheartj/ehv695
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K15311, KAKENHI-PUBLICLY-25136727, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26461056, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15KK0302
[Journal Article] Impact of Updated Diagnostic Criteria for Long QT Syndrome on Clinical Detection of Diseased Patients: Results from Study of Patients Carrying Gene Mutations.2016
- Author(s)
  Hayashi K, Konno T, Fujino N, Itoh H, Fujii Y, Imi-Hashida Y, Tada H, Tsuda T, Tanaka Y, Saito T, Ino H, Kawashiri M, Ohta K, Horie M, Yamagishi.M.
- Journal Title
  
  JACC Clin Electrophysiol
  
  Volume: 2 Issue: 3 Pages: 279-287
- DOI
  10.1016/j.jacep.2016.01.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-26460670, KAKENHI-PROJECT-15KK0302
[Journal Article] Early repolarization and risk of arrhythmia events in long QT syndrome.2016
- Author(s)
  Hasegawa K, Watanabe H, Hisamatsu T, Ohno S, Itoh H, Ashihara T, Hayashi H, Makiyama T, Minamino T, Horie M.
- Journal Title
  
  Int J Cardiol.
  
  Volume: 223 Pages: 540-542
- DOI
  10.1016/j.ijcard.2016.08.215
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-26115008, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-16H05238, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K15306, KAKENHI-PROJECT-16K09431
[Journal Article] Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family2016
- Author(s)
  Ichikawa M, Ohno S, Fujii Y, Ozawa J, Sonoda K, Fukuyama M, Kato K, Kimura H, Itoh H, Hayashi H, Horie M.
- Journal Title
  
  Intern. Med.
  
  Volume: 55 Issue: 3 Pages: 259-262
- DOI
  10.2169/internalmedicine.55.6014
- NAID
  130005122603
- ISSN
  0918-2918, 1349-7235
- Language
  English
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15K19375, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406
[Journal Article] Practical applicability of landiolol, an ultra-short-acting β1-selective blocker, for rapid atrial and ventricular tachyarrhythmias with left ventricular dysfunction.2016
- Author(s)
  Wada Y, Aiba T, Tsujita Y, Itoh H, Wada M, Nakajima I, Ishibashi K, Okamura H, Miyamoto K, Noda T, Sugano Y, Kanzaki, Toshihisa Anzai, Kengo Kusano H, Yasuda S, Horie M, Ogawa H
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: (32) Issue: 2 Pages: 82-88
- DOI
  10.1016/j.joa.2015.09.002
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406
[Journal Article] A novel SCN5A variant associate with drug-induced Brugada Syndrome2016
- Author(s)
  Turker I, Horie M, et al.
- Journal Title
  
  Plos ONE
  
  Volume: 11 Issue: 8 Pages: e0161872-e0161872
- DOI
  10.1371/journal.pone.0161872
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-16K09499
[Journal Article] Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes2016
- Author(s)
 Ichikawa M, Horie M, et al.
- Journal Title
 
 Circ J
 
 Volume: 80 Issue: 12 Pages: 2435-2442
- DOI
 10.1253/circj.CJ-16-0486
- NAID
 130005284992
- ISSN
 1346-9843, 1347-4820
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K19375, KAKENHI-PROJECT-15K09150
[Journal Article] Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular Tachycardia2016
- Author(s)
  Sasaki K, Makiyama T, Yoshida Y, Wuriyanghai Y, Kamakura T, Nishiuchi S, Hayano M, Harita T, Yamamoto Y, Kohjitani H, Hirose S, Chen J, Kawamura M, Ohno S, Itoh H, Takeuchi A, Matsuoka S, Miura M, Sumitomo N, Horie M, Yamanaka S, Kimura T
- Journal Title
  
  PLoS One
  
  Volume: 11 Issue: 10 Pages: e0164795-e0164795
- DOI
  10.1371/journal.pone.0164795
- NAID
  120005860036
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04674, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26291019, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-16K09499
[Journal Article] A type 2 ryanodine receptor variant associated with reduced Ca2+ release and short-coupled torsade de pointe ventricular arrhythmia.2016
- Author(s)
  Fujii Y, Horie M, et al.
- Journal Title
  
  Heart Rhythm
  
  Volume: 14 Issue: 1 Pages: 98-107
- DOI
  10.1016/j.hrthm.2016.10.015
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K08243, KAKENHI-PROJECT-16K08507, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15K09689
[Journal Article] Pediatric Cohort With Long QT Syndrome　– KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms –2016
- Author(s)
 Ozawa, J. Ohno, S. Horie M, et al.
- Journal Title
 
 Circ J
 
 Volume: 80 Issue: 3 Pages: 696-702
- DOI
 10.1253/circj.CJ-15-0933
- NAID
 130005128459
- ISSN
 1346-9843, 1347-4820
- Language
 English
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
 KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406
[Journal Article] The Genetics Underlying Acquired Long QT Syndrome. Impact on Management.2015
- Author(s)
  Itoh H, Crotti L, Aiba T, Spazzplini C, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M.
- Journal Title
  
  European Heart Journal
  
  Volume: 28
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Journal Article] A Common Mutation of Long QT Syndrome Type 1 in Japan2015
- Author(s)
  Itoh H, Dochi K, Shimizu W, Denjoy I, Ohno S, Aiba T, Kimura H, Kato K, Fukuyama M, Hasagawa K, Schulze-Bahr E, Guicheney P, Horie M.
- Journal Title
  
  Circ J
  
  Volume: 79 Issue: 9 Pages: 2026-2030
- DOI
  10.1253/circj.CJ-15-0342
- NAID
  130005095315
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15K19375, KAKENHI-PROJECT-15H04818
[Journal Article] Löffler Endocarditis and Lacking Heart2015
- Author(s)
  Sawayama Y, Itoh H, Sakai H, Horie M.
- Journal Title
  
  Intern. Med.
  
  Volume: 54 Issue: 23 Pages: 3093-3093
- DOI
  10.2169/internalmedicine.54.5622
- NAID
  130005112846
- ISSN
  0918-2918, 1349-7235
- Language
  English
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15H04818
[Journal Article] Asymmetry of parental origin in Long QT syndrome. Preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.2015
- Author(s)
  Itoh H, Berthet M, Fressart V, Denjoy I, Maugenre S, Klug D, Mizusawa Y, Makiyama T, Hofman N, Shimizu W, Wilde AAM, Schulze-Bahr E, Horie M, Tezenas du Montcel S, Guicheney P.
- Journal Title
  
  European Journal of Human Genetics
  
  Volume: - Issue: 8 Pages: 1160-6
- DOI
  10.1038/ejhg.2015.257
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-25461054
[Journal Article] Mosaic KCNJ2 mutation in Andersen-Tawil syndrome: targeted deep sequencing is useful for the detection of mosaicism.2015
- Author(s)
  Hasegawa K, Ohno S, Kimura H, Itoh H, Makiyama T, Yoshida Y, Horie M.
- Journal Title
  
  Clin Genet
  
  Volume: 87 Issue: 3 Pages: 279-83
- DOI
  10.1111/cge.12357
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15H04818
[Journal Article] A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.2014
- Author(s)
  Hasegawa K, Ohno S, Ashihara T, Itoh H, Ding WG, Toyoda F, Makiyama T, Aoki H, Nakamura Y, Delisle BP, Matsuura H, Horie M.
- Journal Title
  
  Heart Rhythm
  
  Volume: 11 Issue: 1 Pages: 67-75
- DOI
  10.1016/j.hrthm.2013.09.073
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23590258, KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460287, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-25461106
[Journal Article] Long QT Syndrome Type8: Novel CACNA1C Mutations Causing QT Prolongation and Variant Phenotypes.2014
- Author(s)
  Fukuyama M, Wang Q, Kato K, Ohno S, Ding WG, Toyoda F, Itoh H, Kimura H, Makiyama T, Ito M, Matsuura H, Horie M.
- Journal Title
  
  Europace.
  
  Volume: in press Issue: 12 Pages: 1828-37
- DOI
  10.1093/europace/euu063
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460287, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-26460295
[Journal Article] Nonsense-mediated mRNA decay due to a CACNA1C splicing mutation in a patient with Brugada syndrome.2014
- Author(s)
  Fukuyama M, Ohno S, Wang Q, Shirayama T, Itoh H, Horie M.
- Journal Title
  
  Heart Rhythm
  
  Volume: 11 Issue: 4 Pages: 629-34
- DOI
  10.1016/j.hrthm.2013.12.011
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460406
[Journal Article] Cardiac channelopathies associated with infantile fatal ventricular arrhythmias: from the cradle to the bench.2014
- Author(s)
  Kato K, Makiyama T, Wu J, Ding WG, Kimura H, Naiki N, Ohno S, Itoh H, Nakanishi T, Matsuura H, Horie M.
- Journal Title
  
  J Cardiovasc Electrophysiol
  
  Volume: 25 Issue: 1 Pages: 66-73
- DOI
  10.1111/jce.12270
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460287, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25461054
[Journal Article] Long-term Pharmacological Therapy of Brugada Syndrome: Is Attenuation of J waves a Marker of Drug Efficacy?2014
- Author(s)
  Hasegawa K, Ashihara T, Kimura H, Jo Hikari, Itoh H, Yamamoto T, Aizawa Y, Horie M.
- Journal Title
  
  Internal Med
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25136705
[Journal Article] Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction2014
- Author(s)
  Ohno S, Omura M, Kawamura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M
- Journal Title
  
  Europace
  
  Volume: in press Issue: 11 Pages: 1646-1654
- DOI
  10.1093/europace/eut382
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460406
[Journal Article] A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.2014
- Author(s)
  Kokunai Y, Nakata T, Furuta M, Sakata S, Kimura H, Aiba T, Yoshinaga M, Osaki Y, Nakamori M, Itoh H, Sato T, Kubota T, Kadota K, Shindo K, Mochizuki H, Shimizu W, Horie M, Okamura Y, Ohno K, Takahashi MP.
- Journal Title
  
  Neurology
  
  Volume: 82 Pages: 1058-64
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25136705
[Journal Article] Long-term pharmacological therapy of Brugada syndrome: is J-wave attenuation a marker of drug efficacy?2014
- Author(s)
  Hasegawa K, Ashihara T, Kimura H, Jo H, Itoh H, Yamamoto T, Aizawa Y, Horie M.
- Journal Title
  
  Intern Med
  
  Volume: 53 Pages: 1523-6
- NAID
  130004466395
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25136705
[Journal Article] Long-term pharmacological therapy of Brugada syndrome: is J-wave attenuation a marker of drug efficacy?2014
- Author(s)
  Hasegawa K, Ashihara T, Kimura H, Jo H, Itoh H, Yamamoto T, Aizawa Y, Horie M.
- Journal Title
  
  Intern Med
  
  Volume: 2014 Pages: 1523-6
- NAID
  130004466395
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25460406
[Journal Article] Mosaic KCNJ2 Mutation in Andersen-Tawil syndrome: Targeted Deep Sequencing is Useful for the Detection of Mosaicism.2014
- Author(s)
  Hasegawa K, Ohno S, Kimura H, Itoh H, Makiyama T, Yoshida Y, Horie M.
- Journal Title
  
  Clin Genet
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25136705
[Journal Article] Gain-of-function KCNH2 mutations in patients with Brugada syndrome.2014
- Author(s)
  Wang Q, Ohno S, Ding WG, Fukuyama M, Miyamoto A, Itoh H, Makiyama T, Wu J, Bai J, Hasegawa K, Shinohara T, Takahashi N, Shimizu A, Matsuura H, Horie M.
- Journal Title
  
  J Cardiovasc Electrophysiol.
  
  Volume: 25 Issue: 5 Pages: 522533-522533
- DOI
  10.1111/jce.12361
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460287, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25461054
[Journal Article] Long-term Pharmacological Therapy of Brugada Syndrome: Is Attenuation of J waves a Marker of Drug Efficacy?2014
- Author(s)
  Hasegawa K, Ashihara T, Kimura H, Jo Hikari, Itoh H, Yamamoto T, Aizawa Y, Horie M.
- Journal Title
  
  Internal Med
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25460406
[Journal Article] A Kir3.4 mutation causes Andersen–Tawil syndrome by an inhibitory effect on Kir2.1.2014
- Author(s)
  Kokunai Y, Nakata T, Furuta M, Sakata S, Kimura H, Aiba T, Yoshinaga M, Osaki Y, Nakamori M, Itoh H, Sato T, Kubota T, Kadota K, Shindo K, Mochizuki H, Shimizu W, Horie M, Okamura Y, Ohno K, Takahashi MP
- Journal Title
  
  Neurology
  
  Volume: 82 Issue: 12 Pages: 1058-64
- DOI
  10.1212/wnl.0000000000000239
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23591245, KAKENHI-PROJECT-24390221, KAKENHI-PROJECT-24591086, KAKENHI-PROJECT-25253016, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25860163, KAKENHI-PROJECT-25713034
[Journal Article] L-type calcium channel mutations in Japanese patients with inherited arrhythmias.2013
- Author(s)
  Fukuyama M, Ohno S, Wang Q, Kimura H, Makiyama T, Itoh H, Ito M, Horie M.
- Journal Title
  
  Circ J
  
  Volume: 77 Pages: 1799-806
- NAID
  10031173762
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25136705
[Journal Article] L-type calcium channel mutations in Japanese patients with inherited arrhythmias.2013
- Author(s)
  Fukuyama M, Ohno S, Wang Q, Kimura H, Makiyama T, Itoh H, Ito M, Horie M.
- Journal Title
  
  Circ J
  
  Volume: 77 Pages: 1534-42
- NAID
  10031173762
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25460406
[Journal Article] Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan.2013
- Author(s)
  Kawamura M, Ohno S, Naiki N, Nagaoka I, Dochi K, Wang Q, Hasegawa K, Kimura H, Miyamoto A, Mizusawa Y, Itoh H, Makiyama T, Sumitomo N, Ushinohama H, Oyama K, Murakoshi N, Aonuma K, Horigome H, Honda T, Yoshinaga M, Ito M, Horie M.
- Journal Title
  
  Circ J
  
  Volume: 77 Pages: 1705-13
- NAID
  10031173750
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25136705
[Journal Article] Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long QT syndrome.2013
- Author(s)
  Duchatelet S, Crotti L, Horie M. et al.
- Journal Title
  
  Circulation Cardiovasc Genet
  
  Volume: 6(4) Issue: 4 Pages: 354-61
- DOI
  10.1161/circgenetics.113.000023
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460406
[Journal Article] Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia2013
- Author(s)
  Itoh H, Horie M
- Journal Title
  
  Circ J
  
  Volume: 77 Issue: 6 Pages: 1534-1542
- DOI
  10.1253/circj.CJ-12-1446
- NAID
  10031158884
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575
[Journal Article] Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan.2013
- Author(s)
  Kawamura M, Ohno S, Naiki N, Nagaoka I, Dochi K, Wang Q, Hasegawa K, Kimura H, Miyamoto A, Mizusawa Y, Itoh H, Makiyama T, Sumitomo N, Ushinohama H, Oyama K, Murakoshi N, Aonuma K, Horigome H, Honda T, Yoshinaga M, Ito M, Horie M.
- Journal Title
  
  Circ J
  
  Volume: 77 Pages: 1705-13
- NAID
  10031173750
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25460406
[Journal Article] A novel gain-of-function KCNJ2 mutation associated with short QT syndrome impairs inward rectification of Kir2.1 currents2012
- Author(s)
  Hattori T, Makiyama T, Akao M, Ehara E, Ohno S, Iguchi M, Nishio Y, Sasaki K, Itoh H, Yokode M, Kita T, Horie M, Kimura T
- Journal Title
  
  Cardiovasc Res
  
  Volume: 93(4) Issue: 3 Pages: 666-673
- DOI
  10.1161/circgenetics.110.958157
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209
[Journal Article] Carvedilol, a Non-Selective .BETA.-with .ALPHA.1-Blocker is Effective in Long QT Syndrome Type 22011
- Author(s)
  Kimura H, Mizusawa Y, Itoh H, Miyamoto A, Kawamura M, Kawaguchi T, Naiki N, Oka Y, Ohno S, Makiyama T, Ito M, Horie M
- Journal Title
  
  J Arrhythmia
  
  Volume: 27 Issue: 4 Pages: 324-331
- DOI
  10.4020/jhrs.27.324
- NAID
  10030721650
- ISSN
  1880-4276, 1883-2148
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209
[Journal Article] KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idio pathic ventricular fibrillation2011
- Author(s)
  Ohno S, Zankov DP, Ding WG, Itoh H, Makiyama T, Doi T, Shizuta S, Hattri T, Miyamoto A, Naiki N, Hancox JC, Matsuura H, Horie M
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: 4 Issue: 3 Pages: 352-361
- DOI
  10.1161/circep.110.959619
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590205, KAKENHI-PROJECT-23390209
[Journal Article] 遺伝性不整脈疾患とシミュレーション2011
- Author(s)
  伊藤英樹、堀江稔、井本敬二
- Journal Title
  
  不整脈+PLUS
  
  Volume: 3 Pages: 9-9
- Data Source
  KAKENHI-PROJECT-23390209
[Journal Article] KCNE2 modulation of Kv4. 3 current and its potential role in fatal rhythm disorders2010
- Author(s)
  Wu J, Itoh H, Horie M, et al
- Journal Title
  
  Heart Rhythm 7
  
  Pages: 199-205
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 遺伝子異常と不整脈2010
- Author(s)
  伊藤英樹, 堀江稔
- Journal Title
  
  臨床と研究 87
  
  Pages: 98-101
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] High prevalence of early repolarization in short QT syndrome2010
- Author(s)
  Watanabe H, Makiyama T, Koyama T, Kannankeril PJ, Seto S, Okamura K, Oda H, Itoh H, Okada M, Tanabe N, Yagihara N, Kamakura S, Horie M, Aizawa Y, Shimizu W.
- Journal Title
  
  Heart Rhythm 7
  
  Pages: 647-652
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] QTが長ければQT延長症候群か?2010
- Author(s)
  伊藤英樹
- Journal Title
  
  Medicina 47
  
  Pages: 66-68
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] Long QT Syndrome with Compound Mutations is Associated with a More Severe Phenotype : a Japanese Multicenter Study2010
- Author(s)
  Itoh H
- Journal Title
  
  Heart Rhythm
  
  Volume: 7 Pages: 1411-1418
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] KCNE2 modulation of KV4.3 current and its potential role in fatal rhythm disorders2010
- Author(s)
  Wu J, Shimizu W, Ding W-G, Ohno S, Toyada F, Itoh H, Zang W-J, Miyamoto Y, Kamakura S, Matsuura H, Nademanee J, Brugada J, Brugada P, Brugada R, Vatta M, Towbin JA, Antzelevitch C, Horie M.
- Journal Title
  
  Heart Rhythm 7
  
  Pages: 199-205
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] QTが長ければQT延長症候群か?2010
- Author(s)
  伊藤英樹
- Journal Title
  
  Medicina
  
  Volume: 47(1) Pages: 66-68
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] 遺伝子異常と不整脈2010
- Author(s)
  伊藤英樹
- Journal Title
  
  臨床と研究 84
  
  Pages: 98-101
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] High prevalence of early repolarization in short QT syndrome2010
- Author(s)
  Watanabe H, Itoh H, Horie M, et al
- Journal Title
  
  Heart Rhythm 7
  
  Pages: 647-652
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 先天性QT延長症候群の遺伝子診断-複数変異例の検討-2010
- Author(s)
  伊藤英樹
- Journal Title
  
  心電図
  
  Volume: 7 Pages: 195-199
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] 遺伝子異常と不整脈2010
- Author(s)
  伊藤英樹
- Journal Title
  
  臨床と研究
  
  Volume: 87(1) Pages: 98-101
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] QTが長ければQT延長症候群か?2010
- Author(s)
  伊藤英樹, 堀江稔
- Journal Title
  
  medicina 47
  
  Pages: 66-68
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] Latent Genetic Background and Molecular Pathogenesis of Drug-Induced Long QT Syndrome2009
- Author(s)
  Hideki Itoh
- Journal Title
  
  Circulation : Arrhythm Electrophysiol 2
  
  Pages: 511-523
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] Latent genetic backgrounds and molecular pathogenesis in drug-induced long QT syndrome2009
- Author(s)
  Itoh H, Sakaguchi T, Ding WS, Watanabe E, Watanabe I, Nishio Y, Makiyama T, Ohno S, Akao M, Higashi Y, Zenda N, Kubota T, Mori C, Okajima K, Haruna T, Miyamoto A, Kawamura M, Ishida K, Nagaoka I, Oka Y, Nakazawa Y, Yao T, Jo H, Sugimoto Y, Ashihara T, Hayashi H, Ito M, Imoto K, Matsuura H, Horie M
- Journal Title
  
  Circulation Arrhythmia & EP 2
  
  Pages: 511-523
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] Latent genetic backgrounds and molecular pathogenesis in drug-induced long QT syndrome.2009
- Author(s)
  Itoh H, Sakaguchi T, Ding WS, Watanabe E, Watanabe I, Nishio Y, Makiyama T, Ohno S, Akao M, Higashi Y, Zenda N, Kubota T, Mori C, Okajima K, Haruna T, Miyamoto A, Kawamura M, Ishida K, Nagaoka I, Oka Y, Nakazawa Y, Yao T, Jo H, Sugimoto Y, Ashihara T, Hayashi H, Ito M, Imoto K, Matsuura H, Horie M
- Journal Title
  
  Circulation Arrhythmia and Electrophysiology 2(5)
  
  Pages: 511-523
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590891
[Journal Article] : Dynamic change in ST-segment and spontaneous occurrence of ventricular fibrillation in brugada syndrome with a novel nonsense mutation in the SCN5AGene during long-term follow-up2009
- Author(s)
  Kawamura M, Ozawa T, Yao T, Ashihara T, Sugimoto Y, Yagi T, Itoh H, Ito M, Makiyama T, Horie M
- Journal Title
  
  Circulation Journal 73(3)
  
  Pages: 584-588
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590891
[Journal Article] Latent genetic backgrounds and molecular pathogenesis in drug-induced long QT syndrome2009
- Author(s)
  Itoh H, Horie M, et al
- Journal Title
  
  Circulation Arrhythmia and Electrophysiology 2(5)
  
  Pages: 511-23
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] A novel KCNH2 mutation as a modifier for short QT interval2009
- Author(s)
  Itoh H, Ashihara T, Nakazawa Y, Yao T, Ito M, et al
- Journal Title
  
  International Journal of Cardiolog URL International Journal of Cardiology
  
  Volume: 137(1) Pages: 83-85
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590891
[Journal Article] Aorto-Pulmonary Artery Dissection.2009
- Author(s)
  Itoh H
- Journal Title
  
  JACC (掲載確定)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome2009
- Author(s)
  Nishio Y, Makiyama T, Itoh H, Sakaguchi T, Ohno S, Gong Y-Z, Yamamoto S, Ozawa T, Ding W-G, Toyoda F, Kawamura M, Akao M, Matsuura H, Kita T, Horie M
- Journal Title
  
  JACC 54
  
  Pages: 812-819
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] A Novel KCNH2 Mutation as a Modifier for Short QT Interval2009
- Author(s)
  Hideki Itoh
- Journal Title
  
  Int J Cardiol 137
  
  Pages: 83-85
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] Aortopulmonary artery dissection2009
- Author(s)
  Hideki Itoh
- Journal Title
  
  J Am Coll Cardiol 54
  
  Pages: 1990-1990
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790718
[Journal Article] Aorto-Pulmonary artery dissection.2009
- Author(s)
  Itoh H, Horie M, et al
- Journal Title
  
  Journal of American College of Cardiology 54(21)
  
  Pages: 1990-1990
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] A Novel KCNH2 Mutation as a Modifier for Short QT Interval.2009
- Author(s)
  Itoh H
- Journal Title
  
  Int J Cardiol (掲載確定)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] Latent genetic backgrounds and molecular pathogenesis in drug-induced long QT syndrome2009
- Author(s)
  Itoh H, Nakazawa Y, Yao T, Ashihara T, Ito M, et al
- Journal Title
  
  Circulation Journal
  
  Volume: 2(5) Pages: 511-523
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590891
[Journal Article] A novel KCNH2 mutation as a modifier for short QT interval2009
- Author(s)
  Itoh H, Sakaguchi T, Ashihara T, Ding G W, Nagaoka I, Oka Y, Nakazawa Y, Yao T, Jo H, Ito M, Matsuura H, Horie M.
- Journal Title
  
  Int J Cardiol. 137
  
  Pages: 83-85
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] Aorto-pulmonary artery dissection2009
- Author(s)
  Itoh H, et al. (7人中1番目)
- Journal Title
  
  J Am Coll Cardiol (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Aortopulmonary artery dissection2009
- Author(s)
  Itoh H, Yamamoto T, Sugihara H, Saotome T, Eguchi Y, Asai T, Horie M
- Journal Title
  
  JACC 54
  
  Pages: 1990-1990
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] A novel KCNH2 mutation as a modifier for short QT interval.2009
- Author(s)
  Itoh H, Sakaguchi T, Ashihara T, Ding G W, Nagaoka I, Oka Y, Nakazawa Y, Yao T, Jo H, Ito M, Matsuura H, Horie M
- Journal Title
  
  URLInternational Journal of Cardiology 137(1)
  
  Pages: 83-85
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590891
[Journal Article] Dynamic change in ST-segment and spontaneous occurrence of ventricular fibrillation in brugada syndrome with a novel nonsense mutation in the SCN5AGene during long-term follow-up2009
- Author(s)
  Kawamura M, Ozawa T, Yao T, Ashihara T, Itoh H, Ito M, et al
- Journal Title
  
  Circulation Journal
  
  Volume: 73(3) Pages: 584-588
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590891
[Journal Article] A novel KCNH2 mutation as a modifier for short QT interval2009
- Author(s)
  Itoh H, Horie M, et al
- Journal Title
  
  Int J Cardiol 137(1)
  
  Pages: 83-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] Hydroxyzine, a First Generation H1-Receptor Antagonist, Inhibits Human Ether-a-go-go?Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation2008
- Author(s)
  Sakaguchi T, Itoh H, Tsuji K, Horie M, et al
- Journal Title
  
  J Pharmacol Sci 108
  
  Pages: 462-471
- NAID
  130000075877
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 家庭用心電計による不整脈の検出-非電送携帯型心電計による検討-2008
- Author(s)
  伊藤誠
- Journal Title
  
  心電図 28
  
  Pages: 21-2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 肺静脈隔離術後患者の心房細動再発の検出における携帯型心電計の有用性2008
- Author(s)
  芦原貴司, 伊藤英樹, 他. (14人中6番目)
- Journal Title
  
  心電図 28(1)
  
  Pages: 77-77
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome2008
- Author(s)
  Makita N, Horie M, Itoh H, et al
- Journal Title
  
  J Clin Invest 118(6)
  
  Pages: 2219-2229
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] QT延長症候群の遺伝子変異2008
- Author(s)
  伊藤英樹
- Journal Title
  
  Heart View 12
  
  Pages: 1106-1110
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] QT延長症候群の遺伝的背景〜先天性と後天性の比較検討2008
- Author(s)
  伊藤英樹, 他. (10人中1番目)
- Journal Title
  
  Bulletin Osaka Heart Club 31
  
  Pages: 21-22
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] QT延長症候群の遺伝子変異2008
- Author(s)
  伊藤英樹
- Journal Title
  
  Heart View 12
  
  Pages: 84-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] A novel SCN5Again-of-function mutation M1875T associated with familial atrial fibrillation2008
- Author(s)
  Makiyama T, Tsuji K, Itoh H, Horie M, et al
- Journal Title
  
  J Am Coll Cardiol 52(16)
  
  Pages: 1326-1334
- NAID
  10024457085
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 薬剤性QT延長症候群の遺伝子異常と分子病態2008
- Author(s)
  伊藤英樹
- Journal Title
  
  循環器専門医 16
  
  Pages: 227-227
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 家庭用心電計による不整脈の検出-非電送携帯型心電計による検討-2008
- Author(s)
  伊藤誠, 伊藤英樹, 他. (11人中6番目)
- Journal Title
  
  心電図 28(1)
  
  Pages: 21-22
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Mutation site dependent variability of cardiac events in LQT2 form of congenital long-QT syndrome2008
- Author(s)
  Nagaoka I, Itoh H, Horie M, et al
- Journal Title
  
  Circ J 72(5)
  
  Pages: 694-699
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 薬剤性QT延長症候群の遺伝子変異と分子病態2008
- Author(s)
  伊藤英樹
- Journal Title
  
  日本循環器学会専門医誌 16
  
  Pages: 227-230
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Age-and genotype-specific triggers for life-threatening arrhythmia in the genotyped long-QT syndrome2008
- Author(s)
  Sakaguchi T, Itoh H, Tsuji K, Horie M, et al
- Journal Title
  
  J Cardiovasc Electrophysiol 19(8)
  
  Pages: 794-799
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 肺静脈隔離術後における心房細動再発と自覚症状 : 携帯型心電計による検討2007
- Author(s)
  芦原貴司, 伊藤英樹, 他. (8人中5番目)
- Journal Title
  
  心電図 27
  
  Pages: 307-316
- NAID
  10019729383
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Brugada症候群と遺伝子病2007
- Author(s)
  牧山武, 赤尾昌治, 伊藤英樹, 堀江稔
- Journal Title
  
  Heart view 11
  
  Pages: 150-157
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] A novel KCNH2 mutation associated with the short QT interval of Brugada syndrome : impaired deactivation for I_<kr> channel.2007
- Author(s)
 Itoh H
- Journal Title
 
 J Am Coll Cardiol 49(abstract)
- Data Source
 KAKENHI-PROJECT-18790496
[Journal Article] A paradoxical effect of lidocaine for the N406S mutation of SCN5A associated with Brugada syndrome2007
- Author(s)
  Itoh H
- Journal Title
  
  Int J Cardiol 121
  
  Pages: 249-252
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] チャネル病の修飾因子:総論2007
- Author(s)
  伊藤英樹
- Journal Title
  
  心臓 39
  
  Pages: 576-579
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] N-and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome2007
- Author(s)
  Ohno S, Tauji K, Itoh H, Horie M, et al
- Journal Title
  
  Heart Rhythm 4(3)
  
  Pages: 332-40
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] 心筋リアノジン受容体の遺伝子変異(I4587V)を有したカテコラミン誘発性多形性心室頻拍の一成人例2007
- Author(s)
  道智賢市, 伊藤英樹, 他(12人中6番目)
- Journal Title
  
  心電図 27
  
  Pages: 246-252
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] A paradoxical effect of lidocaine for the N406S mutation of SCN5A associated with Brugada syndrome2007
- Author(s)
  Itoh H, Tsuji K, Horie M, Imoto K.
- Journal Title
  
  Int J Cardiol 121(3)
  
  Pages: 249-252
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome2007
- Author(s)
  Ohno S, Itoh H, et al. (10人中6番目)
- Journal Title
  
  Heart Rhythm 4
  
  Pages: 332-40
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] A paradoxical effect of lidocaine for the N406S mutation of SCN5Aassociated with Brugada syndrome.2007
- Author(s)
  Itoh H
- Journal Title
  
  International Journal of Cardiology 121
  
  Pages: 239-48
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] チャネル病の修飾因子 : 総論2007
- Author(s)
  伊藤英樹, 他 (11人中1番目)
- Journal Title
  
  心臓 39
  
  Pages: 576-579
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] チャネル病の修飾因子2007
- Author(s)
  伊藤英樹
- Journal Title
  
  心臓 39
  
  Pages: 576-579
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] Variable genetic background between congenital and acquired long-QT syndromes.2007
- Author(s)
  Itoh H
- Journal Title
  
  J Am Coll Cardiol 49(abstract)
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] QT延長症候群2007
- Author(s)
  伊藤英樹
- Journal Title
  
  QT間隔の診かた・考え方
  
  Pages: 131-132
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390212
[Journal Article] Arrhythmogenesis for the short QT syndrome associated with the Combined HERG Channel Gating Defects : a simulation study.2006
- Author(s)
  Itoh H
- Journal Title
  
  Circulation Journal 70
  
  Pages: 502-508
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] 心筋Naチャネルの抗不整脈薬結合関連部位に遺伝子変異を認めたBrugada症候群の薬剤負荷試験と抗不整脈薬治療2006
- Author(s)
  伊藤英樹
- Journal Title
  
  心臓 38
  
  Pages: 777-778
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Dynamic change in ST segment and spontaneous occurrence of ventricular fibrillation in Brugada syndrome with a novel nonsense mutation in the SCN5A gene during long-term follow-up
- Author(s)
  Kawamura M, Itoh H, et al. (10人中7番目)
- Journal Title
  
  Circ J 2009 73
  
  Pages: 584-8
- NAID
  110007126713
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] QT延長症候群の遺伝子変異
- Author(s)
  伊藤英樹, 他. (5人中1番目)
- Journal Title
  
  Heart View 2008 12
  
  Pages: 1106-1110
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] 心房筋リモデリングを考慮したヒト心房細動in silicoモデルにおけるアミオダロンの短期作用と長期作用
- Author(s)
  芦原貴司, 伊藤英樹, 他. (12人中5番目)
- Journal Title
  
  Progress in Medicine 2008 28
  
  Pages: 562-567
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Long and short QT syndromes
- Author(s)
  Horie M, Itoh H.
- Journal Title
  
  Circ J 2007 71
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Single common mutation in the cardiac sodium channel gene SCN5A with diverse clinical phenotypes
- Author(s)
  Makita N, Itoh H, et al. (19人中11番目)
- Journal Title
  
  J Clin Invest 2008 118
  
  Pages: 2219-29
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Aorto-Pulmonary Artery Dissection
- Author(s)
  Itoh h, et.al.
- Journal Title
  
  J Am Coll Cardiol (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] A Novel KCNH2 Mutation as a Modifier for Short QT Interval
- Author(s)
  Itoh H, et al. (12人中1番目)
- Journal Title
  
  Int J Cardiol 2009 (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Arrhythmogenesis for the short QT syndrome associated with the Combined HERG Channel Gating Defects : a simulation study
- Author(s)
  Itoh H, Horie M, Ito M, Imoto K.
- Journal Title
  
  Circ J 2006 70
  
  Pages: 502-508
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Age-related triggers for life-threatening arrhythmia in the genotyped long-QT syndrome
- Author(s)
  Sakaguchi T, Itoh H, et al. (14人中3番目)
- Journal Title
  
  J Cardiovasc Electrophysiol 2008 19
  
  Pages: 794-799
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndrome
- Author(s)
  Nagaoka I, Itoh H, et al. (16人中3番目)
- Journal Title
  
  Circ J 2008 72
  
  Pages: 694-499
- NAID
  110006680544
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] A Novel KCNH2 Mutation as a Modifier for Short QT Interval
- Author(s)
  Itoh H, et.al.
- Journal Title
  
  Int J Cardiol (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Hydroxyzine, a first generation H1-receptor antagonist, inhibits human ether-a-go-go-related gene (HERG) current and causes syncope in a patient with the HERG mutation.
- Author(s)
  Sakaguchi T, Itoh H, et al. (15人中2番目)
- Journal Title
  
  J Pharmacol Sci 2008 108
  
  Pages: 462-71
- NAID
  130000075877
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] Usefulness of fluorine-18-fluorodeoxyglucose positron emission tomography in a patient with Takayasu's arteritis associated with antiphospholipid syndrome
- Author(s)
  Kaku B, Itoh H, et al. (9人中7番目)
- Journal Title
  
  Int Heart J 2006 47
  
  Pages: 311-7
- NAID
  130000068731
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Journal Article] A novel SCN5Again-of-function mutation M1875T associated with familial atrial fibrillation
- Author(s)
  Makiyama T, Itoh H, et al. (13人中10番目)
- Journal Title
  
  J Am Coll Cardiol 2008 118
  
  Pages: 2219-2229
- NAID
  10024457085
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 患者協働とレジリエントな循環器診療を実践するために2023
- Author(s)
  伊藤英樹
- Organizer
  第87回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] マニュアルからの脱却～safety-IIの実践2023
- Author(s)
  伊藤英樹
- Organizer
  第50回日本集中治療医学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] Genetic Aspects of Drug-induced Long QT syndrome: Ion Channel Genes and Race-Specific Variants of CYP genes2023
- Author(s)
  伊藤英樹, 加藤浩一, 中野由紀子, 平塚真弘
- Organizer
  第87回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] Mutation-specific risk stratification for congenital long QT syndrome2022
- Author(s)
  伊藤英樹
- Organizer
  第68回日本不整脈心電学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] 特別演題「薬物と心電図」：薬剤誘発性QT延長症候群の顕在化に関わる薬理学的作用機序2022
- Author(s)
  伊藤英樹
- Organizer
  心電学関連春季大会2022
- Invited
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] 筋強直性ジストロフィーの心伝導障害・不整脈の病態と治療2021
- Author(s)
  伊藤英樹
- Organizer
  筋ジストロフィーの心不全治療
- Invited
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] Enhanced Ca2+ leakage from the network sarcoplasmic reticulum associated with RyR2 with a loss of function mutation: a simulation study2021
- Author(s)
  Hideki Itoh, Minoru Horie, Keiji Imoto
- Organizer
  第67回日本不整脈心電学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] Novel CACNA1C R511Q Mutation, Located in Domain1-2 Linker, with Delayed Calcium Channel Inactivation Causes Non-Syndromic Type-8 Long QT Syndrome2021
- Author(s)
  中島忠, 伊藤英樹, 田村峻太郎, 長谷川寛, 小針尭司, 堀江稔, 倉林正彦, 金古善明
- Organizer
  第86回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] The ABCG2 polymorphism, 421C>A, modifies the pharmacokinetics of apixaban2021
- Author(s)
  Hideki Itoh, Satoshi Ueshima, Karin Hirata, Daiki Hira, Youei Tabuchi, Tomoya Ozawa, Yoshihisa Nakagawa, Minoru Horie, Tomohiro Terada, Toshiya Katsura
- Organizer
  第67回日本不整脈心電学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] Genetic background in patients with idiopathic ventricular fibrillation: known gene screening from whole exome analysis data2018
- Author(s)
  Aiba T, Cha PC, Takahashi A, Ohno S, Kamakura T, Ishikawa T, Ishibashi-Ueda H, Shiba-Harada M, Minamino N, Hayashi K, Yagihara N, Nakano Y, Itoh H, Miyamoto Y, Tanaka T, Makita N, Horie M, Shimizu W, Kusano K, Yasuda S.
- Organizer
  The 83rd Annual Scientific Meeting of the Japanese Circulation Society
- Data Source
  KAKENHI-PROJECT-17K09494
[Presentation] Usefulness of genetic screening for long QT syndrome in the school-based electrocardiographic screening programs2018
- Author(s)
  福山恵、大野聖子、小澤淳一、高山幸一郎、加藤浩一、伊藤英樹、青木寿明、牧山武、堀江稔
- Organizer
  The 83rd Annual Scientific Meeting of the Japanese Circulation Society
- Data Source
  KAKENHI-PROJECT-17K09494
[Presentation] Genetic and clinical aspects of congenital long-QT syndrome: results from the Japanese multicenter registry2018
- Author(s)
  清水渉、山形研一郎、野田崇、草野研吾、宮崎文、牧山武、伊藤英樹、大野聖子、渡部裕、林研至、森田宏、吉永正夫、福田恵一、宮本恵宏、鎌倉史郎、田中敏博、住友直方、萩原誠久、蒔田直昌、堀江稔、相庭武司
- Organizer
  The 83rd Annual Scientific Meeting of the Japanese Circulation Society
- Data Source
  KAKENHI-PROJECT-17K09494
[Presentation] Identification of copy number variations by next generation sequencer in patients with inherited primary arrhythmia syndromes.2017
- Author(s)
  Ichikawa M, Ohno S, Fukumoto D, Takayama K, Wada Y, Fukuyama M, Makiyama T, Itoh H, Horie M
- Organizer
  ESC Congress 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Next-Generation Sequencing Is One of the Promising Ways for Identifying Copy Number Variations in Patients with Inherited Primary Arrhythmia Syndromes.2017
- Author(s)
  Ichikawa M, Ohno S, Fukumoto D, Takayama K, Wada Y, Fukuyama M, Makiyama T, Itoh H, Horie M
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Novel N-Terminal KCNH2 Mutations Identified in Symptomatic Long QT Syndrome Patients.2017
- Author(s)
  Fukumoto D, Ohno S, Wada Y, Fujii Y, Ichikawa M, Takayama K, Fukuyama M, Itoh H, Ding WG, Matsuura H, Horie M
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Triple mutations in three major genes for long QT syndrome are very rare but produce severe phenotypes.2016
- Author(s)
  Ohno S, Wu J, Sonoda K, Itoh H, Makiyama T, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Specific phenotypes caused by RYR2 mutations relate with bradycardia but not with mutation locations in RYR2.2016
- Author(s)
  Ohno S, Ozawa J, Fujii Y, Itoh H, Horie M
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Acquired prolongation of QT interval is really “acquired” or genetic disease?2016
- Author(s)
  Itoh H
- Organizer
  第63回日本不整脈心電学会学術集会遺伝性不整脈国際研究シンポジウム
- Place of Presentation
  札幌
- Year and Date
  2016-07-14
- Invited
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] RYR2 mutations underlying in patients with short-coupled variant of torsade de pointes.2016
- Author(s)
  Fujii Y, Itoh H, Ohno S, Blancard M, Aoki H, Nakagawa Y, Yamamoto S, Matsui Y, Ichikawa M, sonoda K, Ozawa T, Ohkubo K, Watanabe I, Guicheney P, Horie M.
- Organizer
  第80回日本循環器学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2016-03-18
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Various ANK2 mutations in patients with inherited primary arrhythmia syndromes.2016
- Author(s)
  Ichikawa M, Aiba T, Ohno S, Shigemizu D, Ozawa J, Sonoda K, Fukuyama M, Itoh H, Miyamoto Y, Tsunoda T, Makiyama T, Tanaka T, Shimizu W, Horie M
- Organizer
  9th APHRS Scientific Session
- Place of Presentation
  Korea
- Year and Date
  2016-10-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Triple mutations in three major genes for long QT syndrome are very rare and cause complicated phenotypes with ventricular arrhythmia.2016
- Author(s)
  Ohno S, Wu J, Mizusawa Y, Sonoda K, Itoh H, Makiyama T, Horie M
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] AKAP9 mutations identified in young patients with idiopathic ventricular fibrillation or polymorphic ventricular tachycardia2016
- Author(s)
  Sonoda K, Ohno S, Wada Y, Ichikawa M, Fujii Y, Ozawa J, Itoh H, Ashihara T, Hayashi H, Horie M:
- Organizer
  第80回日本循環器学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2016-03-18
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] RYR2 mutations underlying in patients with short-coupled variant of torsade de pointes.2016
- Author(s)
  Fujii Y, Itoh H, Ohno S, Blancard M, Aoki H, Nakagawa Y, Yamamoto S, Matsui Y, Ichikawa M, Sonoda K, Ozawa T, Ohkubo K, Watanabe I, Guicheney P, Horie M
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Specific Phenotypes Caused by RYR2 Mutations Relate with Bradycardia but not with Mutation Locations in RYR2.2016
- Author(s)
  Ohno S, Ozawa J, Fujii Y, Itoh H, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] A novel CACNA1C mutation identified in a patient with atypical Timothy syndrome exerts both loss- and gain-of-function effects on Cav1.2.2016
- Author(s)
  Ozawa J, Ohno S, Toyoda F, Itoh H, Fukuyama M, Harita T, Makiyama T, Hiroshi Suzuki, Akihiko Saitoh, Matsuura H, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Nonsense-Mediated mRNA Decay due to a CACNA1C Splicing Mutation in a Patient with Brugada Syndrome2015
- Author(s)
  Fukuyama M, Ohno S, Wang Q, ShirayamaT，Itoh H, Horie M:
- Organizer
  第30回日本不整脈学会学術大会
- Place of Presentation
  京都
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Nonsense-Mediated mRNA Decay due to a CACNA1C Splicing Mutation in a Patient with Brugada Syndrome2015
- Author(s)
  Fukuyama M, Ohno S, Wang Q, ShirayamaT，Itoh H, Horie M.
- Organizer
  第30回日本不整脈学会学術大会
- Place of Presentation
  京都
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] 完全房室ブロックに伴いTorsade de Pointesを来たし，Tpeak-Tend延長が発作予測に有効であることが示唆された一例．2015
- Author(s)
  諸戸礼知安，加藤浩一，藤居祐介，小澤友哉，芦原貴司，伊藤英樹，堀江稔.
- Organizer
  第63回日本心臓病学会学術集会
- Place of Presentation
  横浜
- Year and Date
  2015-09-18
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Genetics of ventricular fibrillation with short-coupled torsade de pointes.2015
- Author(s)
  Malorie Blancard, Estelle Gandjbakhch, Fabrice Extramiana, Vincent Probst, Michel Haissaguerre, Hideki Itoh, Pascale Guicheney
- Organizer
  Printemps de la Cardiologie
- Place of Presentation
  Dijon
- Year and Date
  2015-04-07
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Arrhythmogenic ventricular cardiomyopathy with peculiar ventricular aneurysm and TMEM43 mutations.2015
- Author(s)
  Ichikawa M, Ohno S, Fujii Y, Ozawa J, Sonoda K, Fukuyama M, Kato K, Itoh H,Horie M.
- Organizer
  EHRA EUROPACE CARDIOSTIM 2015
- Place of Presentation
  Milan
- Year and Date
  2015-06-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Short-coupled variant of torsade de pointesに対するverapamilの有効性2015
- Author(s)
  藤居祐介、伊藤英樹、小澤友哉、服部哲久、芦原貴司、八木典章、松本祐一、木村紘美、酒井　宏、山本　孝、林　秀樹、大野聖子、堀江　稔、中川義久、山本　聖、松井由美恵
- Organizer
  第13回特発性心室細動研究会
- Place of Presentation
  東京
- Year and Date
  2015-02-14
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] The genetics underlying the acquired long QT syndrome. Impact on management.2015
- Author(s)
  Itoh H, Spazzolini C, Crotti L, Aiba T, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M.
- Organizer
  The Heart Rhythm Society's 36th Annual Scientific Sessions
- Place of Presentation
  Boston
- Year and Date
  2015-05-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] 小児ＱＴ延長症候群:ＬＱＴ２は発症年齢が高いが重症例が多い2015
- Author(s)
  小澤淳一, 大野聖子, 伊藤英樹, 牧山　武, 堀江　稔
- Organizer
  第26回滋賀不整脈研究会
- Place of Presentation
  滋賀
- Year and Date
  2015-02-28
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Usefulness of Benchtop Next Generation Sequencer in Research of Inherited Primary Arrhythmia Syndromes2015
- Author(s)
  Ohno S,Fukuyama M,Itoh H,Makiyama T,Horie M
- Organizer
  第79回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Short-coupled variant of torsade de pointesに対するverapamilの有効性2015
- Author(s)
  藤居祐介、伊藤英樹、小澤友哉、服部哲久、芦原貴司、八木典章、松本祐一、木村紘美、酒井　宏、山本　孝、林　秀樹、大野聖子、堀江　稔、中川義久、山本　聖、松井由美恵
- Organizer
  第13回特発性心室細動研究会
- Place of Presentation
  東京
- Year and Date
  2015-02-14
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] The genetics underlying the acquired long QT syndrome. Impact on management.2015
- Author(s)
  Itoh H, Spazzolini C, Crotti L, Aiba T, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M.
- Organizer
  The Heart Rhythm Society's 36th Annual Scientific Sessions
- Place of Presentation
  アメリカ合衆国
- Year and Date
  2015-05-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Arrhythmogenic ventricular cardiomyopathy with peculiar ventricular aneurysm and TMEM43 mutations2015
- Author(s)
  Ichikawa M, Ohno S, Fujii Y, Ozawa J, Sonoda K, Fukuyama M, Kato K, Itoh H,Horie M
- Organizer
  EUROPACE- CARDIOSTIM 2015
- Place of Presentation
  イタリア
- Year and Date
  2015-06-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] 完全房室ブロックに伴いTorsade de Pointesを発症した二次性QT延長症候群の１例2015
- Author(s)
  諸戸礼知安, 加藤浩一, 藤居祐介, 小澤友哉, 芦原貴司, 伊藤英樹, 堀江　稔
- Organizer
  第207回日本内科学会近畿地方会
- Place of Presentation
  大阪
- Year and Date
  2015-03-07
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] 慢性心房細動の治療戦略. 自験例と理論的見地から.2015
- Author(s)
  坂田憲祐，小澤友哉，芦原貴司，加藤浩一，藤居祐介，服部哲久，伊藤英樹，杉本喜久，堀江　稔.
- Organizer
  第30回京滋奈良ハートリズム研究会
- Place of Presentation
  京都
- Year and Date
  2015-05-23
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Differential Diagnosis of Catecholaminergic Polymorphic Ventricular Tachycardia vs. Long QT Syndrome Type 1: A Modified Schwartz Scoring2015
- Author(s)
  Ozawa J, Ohno S, Fujii Y, Makiyama T, Suzuki H, Saitoh A, Horie M.
- Organizer
  AHA Scientific Sessions 2015
- Place of Presentation
  アメリカ合衆国
- Year and Date
  2015-11-07
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] 小児ＱＴ延長症候群:ＬＱＴ２は発症年齢が高いが重症例が多い2015
- Author(s)
  小澤淳一, 大野聖子, 伊藤英樹, 牧山　武, 堀江　稔
- Organizer
  第26回滋賀不整脈研究会
- Place of Presentation
  滋賀
- Year and Date
  2015-02-28
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] 薬剤負荷による遺伝子型の予測が困難であった QT 延長症候群の一例.2015
- Author(s)
  中村恵理子、伊藤英樹、藤居祐介、加藤浩一、澤山裕一、八木典章、松本祐一、福山恵、服部哲久、木村紘美、小澤友哉、芦原貴司、酒井宏、山本孝、林秀樹、福原武久、堀江稔.
- Organizer
  第119回日本循環器学会近畿地方会
- Place of Presentation
  大阪
- Year and Date
  2015-06-20
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] 完全房室ブロックに伴いTorsade de Pointesを発症した二次性QT延長症候群の１例2015
- Author(s)
  諸戸礼知安, 加藤浩一, 藤居祐介, 小澤友哉, 芦原貴司, 伊藤英樹, 堀江　稔
- Organizer
  第207回日本内科学会近畿地方会
- Place of Presentation
  大阪
- Year and Date
  2015-03-07
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Usefulness of Benchtop Next Generation Sequencer in Research of Inherited Primary Arrhythmia Syndromes.2015
- Author(s)
  Ohno S,Fukuyama M,Itoh H,Makiyama T,Horie M.
- Organizer
  第79回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] 後天性QT延長症候群の発症病態2014
- Author(s)
  伊藤英樹、Crotti Lia、Schwartz J Peter、林研至、中島忠、大野聖子、牧山武、山岸正和、井本敬二、Pascale Guicheney、堀江稔
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島
- Invited
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] 後天性QT延長症候群の発症病態2014
- Author(s)
  伊藤英樹、Crotti Lia、Schwartz J Peter、林研至、中島忠、大野聖子、牧山武、山岸正和、井本敬二、Pascale Guicheney、堀江稔
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島
- Invited
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Kir3.4変異はKir2.1に対する抑制作用を通してAndersen-Tawil 症候群を引き起こす2014
- Author(s)
  田充、殻内洋介、中田智彦、坂田宗平、木村紘美、相庭武司、吉永正夫、大崎裕亮、中森雅之、伊藤秀樹、佐藤貴子、久保田智哉、門田一繁、進藤克郎、望月秀樹、清水渉、堀江稔、岡村康司、大野欽司、高橋正紀
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Both Gain- and Loss-of-Function SCN5A Mutations Associated with Infantile Fatal Ventricular Arrhythmias2014
- Author(s)
  Koichi Kato, Takeru Makiyama, Jie Wu, Wei-Guang Ding, Hiromi Kimura, Nobu Naiki, Seiko Ohno, Hideki Itoh, Toshio Nakanishi, Hiroshi Matsuura, Minoru Horie
- Organizer
  ACC 2014
- Place of Presentation
  Washington
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Kir3.4変異はKir2.1に対する抑制作用を通してAndersen-Tawil 症候群を引き起こす2014
- Author(s)
  古田充、殻内洋介、中田智彦、坂田宗平、木村紘美、相庭武司、吉永正夫、大崎裕亮、中森雅之、伊藤秀樹、佐藤貴子、久保田智哉、門田一繁、進藤克郎、望月秀樹、清水渉、堀江稔、岡村康司、大野欽司、高橋正紀
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Copy number variation in KCNQ1 gene were frequently identified in the pediatric patients of long QT syndrome and caused exercise related QT prolongation.2013
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M.
- Organizer
  ESC CONGRESS 2013
- Place of Presentation
  Amsterdam, The Netherlands
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] The High Prevalence of Early Repolarization in Genotyped Long QT Syndrome.2013
- Author(s)
  Hasegawa K, Watanabe H, Ohno S, Itoh H, Makiyama T, Ashihara T, Hayashi H, Horie M.
- Organizer
  AHA Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Asymmetry of parental origin in Long QT syndrome2013
- Author(s)
  Itoh H, Horie M
- Organizer
  European Human Genetics Conference
- Place of Presentation
  Paris, France
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Novel CACNA1C mutations in Long QT syndrome patients- The subtype of Long QT syndrome type 8.2013
- Author(s)
  Fukuyama M, Wang Q, Kato K, Ohno S, Kimura H, Makiyama T, Itoh H, Ito M, Matsuura H, Horie M.
- Organizer
  Denis Escande Symposium
- Place of Presentation
  Amsterdam, the Netherlands
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Exon-3 deletion of RyR2 encoding cardiac ryanodine receptor related to left ventricular non-compaction (LVNC) with ventricular arrhythmia and bradycardia.2013
- Author(s)
  Ohno S, Omura M, Kawamura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M.
- Organizer
  EHRA EUROPACE
- Place of Presentation
  Athens, Greek
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] 若年時に診断された催不整脈性右室心筋症・異形成（ARVC/D）患者の臨床的および遺伝的特徴2013
- Author(s)
  大野聖子、福山恵、長谷川奏恵、木村紘美、伊藤英樹、牧山武、堀江稔
- Organizer
  第30回日本心電学会
- Place of Presentation
  青森
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Phenotypic characterization of three patients with lethal arrhythmia related to KCNH2-R148W missense mutation.2013
- Author(s)
  Ohno S, Wang Q, Hasegwas K, Itoh H, Makiyama T, Horie M.
- Organizer
  6th APHRS & CardioRhythm
- Place of Presentation
  Hong Kong, China
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Altered splicing of cardiac sodium channel might be responsible for cardiac conduction defects in myotonic dystrophy.2013
- Author(s)
  Kokunai Y, Kino Y, Li M, Itoh H, Nakamori M, Kimura T, Matsumura T, Fujimura H, Nukina N, Sakoda S, Horie M, Imoto K, Ishiura S, Swanson MS, Charlet-Berguerand N, Takahashi MP.
- Organizer
  the 9th International Myotonic Dystrophy Consortium
- Place of Presentation
  Basque, Spain
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Copy number variation in KCNQ1 gene were frequently identified in the pediatric patients of long QT syndrome and caused exercise related QT prolongation.2013
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M.
- Organizer
  ESC CONGRESS
- Place of Presentation
  Amsterdam, the Netherlands
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] 心室細動後の12誘導心電図で広範囲なST上昇を認めたJ wave syndromeの一例2013
- Author(s)
  冨田行則、服部哲久、伊藤英樹、児玉　健二、福沢綾子、高橋宏明、八木典章、木村紘美、山科　聡、酒井　宏、小澤友哉、山本　孝、伊藤　誠、堀江　稔
- Organizer
  第115回日本循環器学会近畿地方会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] VerapamilがVF stormに有効であった突発性心室細動の１例2013
- Author(s)
  藤居祐介、伊藤英樹、服部哲久、小澤友哉、芦原貴司、児玉健二、高橋宏明、福沢綾子、冨田行則、八木典章、松本祐一、内貴乃生、木村紘美、酒井　宏、山本　孝、伊藤　誠、堀江　稔
- Organizer
  第75回滋賀県循環器疾患研究会
- Place of Presentation
  滋賀
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] VerapamilがVF stormに有効であった突発性心室細動の１例2013
- Author(s)
  藤居祐介、伊藤英樹、服部哲久、小澤友哉、芦原貴司、児玉健二、高橋宏明、福沢綾子、冨田行則、八木典章、松本祐一、内貴乃生、木村紘美、酒井　宏、山本　孝、伊藤　誠、堀江　稔
- Organizer
  第75回滋賀県循環器疾患研究会
- Place of Presentation
  滋賀
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Asymmetry of parental origin in Long QT syndrome.2013
- Author(s)
  Itoh H, Berthet M, Fressart V, Denjoy I , Maugenre S, Klug D, Mizusawa Y, Makiyama T, Hofman N, Husemann A, Shimizu W, Wilde AA , Schulze-Bahr E, Horie M, du Montcel ST, Guicheney P.
- Organizer
  European Human Genetics Conference
- Place of Presentation
  Paris, France
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Exon-3 deletion of RyR2 encoding cardiac ryanodine receptor related to left ventricular non-compaction (LVNC) with ventricular arrhythmia and bradycardia.2013
- Author(s)
  Ohno S, Omura M, Kawamura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M.
- Organizer
  EHRA EUROPACE 2013
- Place of Presentation
  Athens, Greek
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] 心室細動後の12誘導心電図で広範囲なST上昇を認めたJ wave syndromeの一例2013
- Author(s)
  冨田行則、服部哲久、伊藤英樹、児玉　健二、福沢綾子、高橋宏明、八木典章、木村紘美、山科　聡、酒井　宏、小澤友哉、山本　孝、伊藤　誠、堀江　稔
- Organizer
  第115回日本循環器学会近畿地方会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Asymmetry of parental origin in Long QT syndrome. European Human Genetics Conference2013
- Author(s)
  Itoh H, Berthet M, Fressart V, Denjoy I , Maugenre S, Klug D, Mizusawa Y, Makiyama T, Hofman N, Husemann A, Shimizu W, Wilde AA , Schulze-Bahr E, Horie M, du Montcel ST, Guicheney P.
- Organizer
  European Human Genetics Conference
- Place of Presentation
  Paris, France
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Altered splicing of cardiac sodium channel might be responsible for cardiac conduction defects in myotonic dystrophy.2013
- Author(s)
  Kokunai Y, Kino Y, Li M, Itoh H, Horie M. et al.
- Organizer
  the 9th International Myotonic Dystrophy Consortium
- Place of Presentation
  Basque, Spain
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] short-coupled variant of torsade de pointes の遺伝的背景2013
- Author(s)
  堀本かんな、伊藤英樹、小澤友哉、内貴乃生、冨田行則、藤居祐介、八木典章、服部哲久、木村紘美、芦原貴司、松本祐一、酒井　宏、山本　孝、伊藤　誠、堀江　稔
- Organizer
  第116回日本循環器学会近畿地方会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Phenotypic characterization of three patients with lethal arrhythmia related to KCNH2-R148W missense mutation.2013
- Author(s)
  Ohno S, Wang Q, Hasegwas K, Itoh H, Makiyama T, Horie M.
- Organizer
  6th APHRS & CardioRhythm 2013
- Place of Presentation
  Hong Kong, China
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] KCNH2遺伝子変異による徐脈性QT延長症候群の一家系2013
- Author(s)
  中泉伸彦、伊藤英樹、児玉　浩、富田行則、八木典章、服部哲久、木村紘美、酒井　宏、小澤友哉、山本　孝、伊藤　誠、堀江　稔、椙本　晃
- Organizer
  第115回日本循環器学会近畿地方会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Novel CACNA1C mutations in Long QT syndrome patients- The subtype of Long QT syndrome type 8.2013
- Author(s)
  Fukuyama M, Wang Q, Kato K, Ohno S, Kimura H, Makiyama T, Itoh H, Ito M, Matsuura H, Horie M.
- Organizer
  Denis Escande Symposium 2013
- Place of Presentation
  Amsterdam, the Netherlands
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Underlying Mechanisms in Forme Fruste Long QT Syndrome Manifested by Acquired Factors.2013
- Author(s)
  Itoh H.
- Organizer
  The 2nd HD Physiology International Symposium
- Place of Presentation
  Tokyo, Japan
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Phenotypic characterization of three patients with lethal arrhythmia related to KCNH2-R148W missense mutation.2013
- Author(s)
  Ohno S, Wang Q, Hasegwas K, Itoh H, Makiyama T, Horie M.
- Organizer
  6th APHRS & CardioRhythm 2013.
- Place of Presentation
  Hong Kong, China
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Copy number variation in KCNQ1 gene were frequently identified in the pediatric patients of long QT syndrome and caused exercise related QT prolongation.2013
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M.
- Organizer
  ESC CONGRESS 2013
- Place of Presentation
  Amsterdam, the Netherlands
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] The High Prevalence of Early Repolarization in Genotyped Long QT Syndrome.2013
- Author(s)
  Ohno S, Itoh H, Horie M. et al.
- Organizer
  AHA Scientific Sessions 2013．
- Place of Presentation
  Dallas, Texas, U.S.A.
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Altered splicing of cardiac sodium channel might be responsible for cardiac conduction defects in myotonic dystrophy.2013
- Author(s)
  Kokunai Y, Kino Y, Li M, Itoh H, Nakamori M, Kimura T, Matsumura T, Fujimura H, Nukina N, Sakoda S, Horie M, Imoto K, Ishiura S, Swanson MS, Charlet-Berguerand N, Takahashi MP.
- Organizer
  The 9th International Myotonic Dystrophy Consortium
- Place of Presentation
  Basque, Spain
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] short-coupled variant of torsade de pointes の遺伝的背景2013
- Author(s)
  堀本かんな、伊藤英樹、小澤友哉、内貴乃生、冨田行則、藤居祐介、八木典章、服部哲久、木村紘美、芦原貴司、松本祐一、酒井　宏、山本　孝、伊藤　誠、堀江　稔
- Organizer
  第116回日本循環器学会近畿地方会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] KCNH2遺伝子変異による徐脈性QT延長症候群の一家系2013
- Author(s)
  中泉伸彦、伊藤英樹、児玉　浩、富田行則、八木典章、服部哲久、木村紘美、酒井　宏、小澤友哉、山本　孝、伊藤　誠、堀江　稔、椙本　晃
- Organizer
  第115回日本循環器学会近畿地方会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Underlying Mechanisms in Forme Fruste Long QT Syndrome Manifested by Acquired Factors.2013
- Author(s)
  Itoh H.
- Organizer
  The 2nd HD Physiology International Symposium
- Place of Presentation
  Tokyo, Japan
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] 若年時に診断された催不整脈性右室心筋症・異形成（ARVC/D）患者の臨床的および遺伝的特徴2013
- Author(s)
  大野聖子、福山恵、長谷川奏恵、木村紘美、伊藤英樹、牧山武、堀江稔
- Organizer
  第30回日本心電学会
- Place of Presentation
  青森
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Asymmetry of parental origin in Long QT syndrome.2013
- Author(s)
  Itoh H, Berthet M, Horie M. et al.
- Organizer
  European Human Genetics Conference
- Place of Presentation
  Paris, France
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] The High Prevalence of Early Repolarization in Genotyped Long QT Syndrome.2013
- Author(s)
  Hasegawa K, Watanabe H, Ohno S, Itoh H, Makiyama T, Ashihara T, Hayashi H, Horie M.
- Organizer
  AHA Scientific Sessions
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Underlying Mechanisms in Forme Fruste Long QT Syndrome Manifested by Acquired Factors.2013
- Author(s)
  Itoh H.
- Organizer
  The 2nd HD Physiology International Symposium
- Place of Presentation
  Tokyo, Japan
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] QT延長症候群における変異遺伝子の伝達乖離―多施設国際共同研究―2012
- Author(s)
  伊藤英樹
- Organizer
  第27回日本不整脈学会学術大会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Seasonal and circadian distributions of occurrence of cardiac events in genotyped patients with congenital long QT syndrome2011
- Author(s)
  Takigawa M, Kawamura M, Noda T, Yamada Y, Okamura H, Satomi K, Aiba T, Aihara N, Kamakura S, Sakaguchi T, Mizusawa Y, Itoh H, Horie M, Shimizu W
- Organizer
  第75回日本循環器学会総会・学術集会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Site-specific arrhythmogenesis in structurally normal heart of non-Brugada patients with ventricular arrhythmias originating from ventricular outflow tract2011
- Author(s)
  Ozawa T, Ito M, Itoh H, Nakazawa Y, Sugimoto Y, Yao T, Miyamoto A, Ashihara T, Horie M
- Organizer
  APHRS2011 & 26th JHRS 28th JSE合同学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Long QT syndromes are heterogeneous disease entities presenting not only QT prolongation but multiple phenotypes-cases with compound heterozygous mutations2011
- Author(s)
  Horie M, Itoh H, Shimizu W, Hayashi K, Ohno S, Makiyama T, Yamagishi M, Kamakura S
- Organizer
  APHRS2011 & 26th JHRS 28th JSE合同学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Clinical and genetic characterization of Japanese patients with arrhythmogenic right ventricular cardiomyopathy2011
- Author(s)
  Ohno S, Nishio Y, Nagaoka I, Miyamoto A, Kimura H, Itoh H, Makiyama T, Horie M
- Organizer
  ICPES 2011
- Place of Presentation
  Athens, Greece
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Genotype-phenotype correlation in Japanese patients with andersen-tawil syndrome2011
- Author(s)
  Kimura H, Zhou J, Itoh H, Mizusawa Y, Miyamoto A, Jitoh Y, Kawamura M, Sakaguchi T, Nishio Y, Ding WG, Makiyama T, Ito M, Matsuura H, Horie M
- Organizer
  第75回日本循環器学会総会・学術集会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] 携帯型イベント心電計を活用した日常診療2011
- Author(s)
  伊藤誠
- Organizer
  第28回日本心電学会学術集会ランチョンセミナー(オムロン)
- Place of Presentation
  福岡
- Year and Date
  2011-09-21
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Phenotype variability in patients carrying KCNJ2 mutations2011
- Author(s)
  Kimura H, Zhou J, Itoh H., Mizusawa Y, Miyamoto A, Kawamura M, Makiyama T, Ito M, Matsuura H, Horie H
- Organizer
  ESC Congress 2011
- Place of Presentation
  Paris, France
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] 携帯型イベント心電計を活用した日常診療2011
- Author(s)
  伊藤誠
- Organizer
  第28回日本心電学会学術集会ランチョンセミナー
- Place of Presentation
  福岡市
- Year and Date
  2011-09-21
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] KCNE5 variants are novel modulators of brugada syndrome and idiopathic ventri-cular fibrillation2011
- Author(s)
  Ohno S, Zankov DP, Ding WG, Itoh H, Makiyama T, Doi T, Shizuta S, Hattori T, Miyamoto A, Naiki N, Matsuura H, Horie M
- Organizer
  APHRS2011 & 26th JHRS 28th JSE合同学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Over-expression of heterozygous KCNJ2-M301K channels, identified in a patient with short QT syndrome, shortened action potential durations in neonatal rat ventricular myocytes2011
- Author(s)
  Hattori T, Makiyama T, Akao M, Ehara E, Ohno S, Iguchi M, Sasaki K, Itoh H, Horie M, Kimura T
- Organizer
  ESC Congress 2011
- Place of Presentation
  Paris, France
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Long QT Syndromes are heterogeneous disease entities presenting not only QT prolongation but multiple phenotypes Cases with compound heterozygous mutations2011
- Author(s)
  Horie M, Itoh H, Shimizu W, Hayashi K, Ohno S, Makiyama T, Yamagishi M, Kamakura S
- Organizer
  APHRS2011 & 26th JHRS 28th JSE合同学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] What influences β-blocker resistance for secondary prevention of cardiac events in patients with congenital long QT syndrome2011
- Author(s)
  Makimoto H, Horie M, Ogawa S, Aizawa Y, Ohe T, Kusano K, Yamagishi M, Makita N, Tanaka T, Makiyama T, Yoshinaga M, Hagiwara N, Sumitomo N, Itoh H, Yamada Y, Okamura, Noda T, Aiba T, Kamakura S, Miyamoto Y, Shimizu W
- Organizer
  第75回日本循環器学会総会・学術集会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Clinical differences between KCNH2 and SCN5A mutation carriers with Brugada syndrome and Brugada-like ECG patients in Japan2011
- Author(s)
  Ohno S, Miyamoto A, T Makiyama, Itoh H, Horie M
- Organizer
  AHA Scientific Sessions 2011
- Place of Presentation
  Orlando, Florida, U.S.A.
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] Mutations of the cardiac ryanodine Recepter (RyR2) gene in catecholaminergic polymorphic ventricular tachycardia2011
- Author(s)
  Kawamura M, Nagaoka I, Kenichi, Nishio Y, Itoh H, Kimura H, Miyamoto A, Mizusawa Y, Jito Y, Ishida K, Ito M, Makiyama T, Ohno S, Sumitomo N, Oyama K, Horie M
- Organizer
  APHRS2011 & 26th JHRS 28th JSE合同学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] 学校検診にて発見された早期再分極症候群(J wave syndrome)の疑われる一例2011
- Author(s)
  岡川浩人、鹿野真由美、西山敬三、松井俊樹、山岡修、大村具子、伊藤誠、堀江稔
- Organizer
  第70回滋賀県循環器疾患研究会
- Place of Presentation
  滋賀
- Year and Date
  2011-06-11
- Data Source
  KAKENHI-PROJECT-23390209
[Presentation] J波を伴う突発性心室細動におけるデバイス治療の工夫と有効性日本不整脈学会2010
- Author(s)
  八尾武憲, 水澤有香, 中澤優子, 宮本証, 伊藤英樹, 芦原貴司, 杉本喜久, 伊藤誠, 堀江稔, 城日加里
- Organizer
  第2回植え込みデバイス関連冬季大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Irrigation catheterを用いた肺静脈隔離術における食道温測定の意義2010
- Author(s)
  伊藤誠
- Organizer
  第20回京滋奈良ハートリズム研究会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21790718
[Presentation] Influence of pulmonary vein isolation on heart rate : A clinical study using event-ECG monitors.2010
- Author(s)
  Nakazawa Y, Ashihara T, Miyamoto A, Ozawa T, Itoh H, Sugimoto Y, Ito M, Horie M
- Organizer
  APHRS2010/APAFS2010
- Place of Presentation
  Jeju Island Korea
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] What is the Best Index of Successful Ablation in Each Radiofrequency Point Using Irrigation Catheter for Pulmonary Vein Isolation?2010
- Author(s)
  伊藤誠
- Organizer
  第74回日本循環器学会総会・学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Irrigated ablation systemによる左房後壁の電位波高低下は安全な焼灼の指標となるか?2010
- Author(s)
  伊藤誠
- Organizer
  第27回日本心電学会学術集会
- Place of Presentation
  大分
- Data Source
  KAKENHI-PROJECT-21790718
[Presentation] Irrigation catheterを用いた肺静脈隔離術における食道温測定の意義2010
- Author(s)
  伊藤誠
- Organizer
  第20回京滋奈良ハートリズム研究会
- Place of Presentation
  京都市
- Year and Date
  2010-02-13
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] J波を伴う突発性心室細動におけるデバイス治療の工夫と有効性日本不整脈学会2010
- Author(s)
  八尾武憲, 伊藤誠et al
- Organizer
  第2回植え込みデバイス関連冬季大会
- Place of Presentation
  東京都
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 12誘導心電図による予後研究2010
- Author(s)
  宮本証, 石田勝也, 林秀樹, 吉野知秀, 水澤有香, 杉本嘉久, 伊藤誠, Joel Q.Xue, 堀江稔
- Organizer
  第20回京滋奈良ハートリズム研究会
- Place of Presentation
  京都
- Year and Date
  2010-02-13
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Irrigation catheterを用いた肺静脈隔離術における食道温測定の意義2010
- Author(s)
  伊藤誠
- Organizer
  第20回京滋奈良ハートリズム研究会
- Place of Presentation
  京都
- Year and Date
  2010-02-13
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Latent genetic backgrounds and molecular pathogenesis inacquired long QT syndrome with distinct arrhythmic triggers2010
- Author(s)
  Itoh H, Ito M, et al
- Organizer
  AHA Scientific Sessions
- Place of Presentation
  Chicago Illinois USA
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] シンポジウムLatent Genetic Backgrounds of Acquired Long QT Syndrome2010
- Author(s)
  Hideki Itoh
- Organizer
  第74回日本循環器学会総会学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21790718
[Presentation] 携帯型イベント心電計を活用した日常診療2010
- Author(s)
  伊藤誠
- Organizer
  第27回日本心電学会学術集会
- Place of Presentation
  大分iichiko総合文化センター
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Latent genetic backgrounds and molecular pathogenesis in acquired long QT syndrome with distinct arrhythmic triggers..2010
- Author(s)
  Itoh H, Oka Y, Ding WG, Sakaguchi T, Kimura H, Mizusawa Y, Miyamoto A, Wu J, Ohno S, Makiyama T, Ito M, Matsuura H, Horie M
- Organizer
  AHA Scientific Sessions 2010
- Place of Presentation
  Chicago Illinois U.S.A
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Long QT syndrome with compound mutations is associated with a severer phenotype : a Japanese multicenter study2010
- Author(s)
  Itoh H
- Organizer
  European Heart Association (ESC)
- Place of Presentation
  Stockholm, Sweden
- Data Source
  KAKENHI-PROJECT-21790718
[Presentation] 12誘導心電図による予後研究2010
- Author(s)
  宮本証、伊藤誠、et al
- Organizer
  第20回京滋奈良ハートリズム研究会
- Place of Presentation
  京都市
- Year and Date
  2010-02-13
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Latent genetic backgrounds and molecular pathogenesis in acquired long QT syndrome with distinct triggers2010
- Author(s)
  Itoh H
- Organizer
  American Heart Association (AHA)
- Place of Presentation
  Chicago, U.S.A.
- Data Source
  KAKENHI-PROJECT-21790718
[Presentation] Irrigated ablation systemによる左房後壁の電位波高低下は安全な焼灼の指標となるか?2010
- Author(s)
  伊藤誠、et al
- Organizer
  第27回日本心電学会学術集会
- Place of Presentation
  大分iichiko総合文化センター
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Latent genetic backgrounds and molecular pathogenesis of drug-induced long QT syndrome2009
- Author(s)
  Itoh H, et al. (13人中1番目)
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 多種類の上室頻拍を合併した心臓手術後の一例2009
- Author(s)
  城日加里, 八尾武憲, 山科聡, 中澤優子, 伊藤英樹, 芦原貴司, 杉本喜久, 伊藤誠, 堀江稔, 八木崇文
- Organizer
  第24回日本不整脈学会学術大会第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 多種類の上室頻拍を合併した心臓手術後の一例2009
- Author(s)
  城日加里, 八尾武憲, 山科聡, 中澤優子, 伊藤英樹, 芦原貴司, 杉本喜久, 伊藤誠, 堀江稔, 八木崇文
- Organizer
  第24回日本不整脈学会学術大会第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] 冠動脈洞開口以上を合併した防湿回帰性頻拍にカテーテル・アブレーションを施行し根治しえた1例2009
- Author(s)
  伊藤英樹, 八尾武憲, 宮本証, 中澤優子, 城日加里, 水澤有香, 芦原貴司, 八木崇文, 横田良司, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第21回カテーテル・アブレーション委員会公開研究会
- Place of Presentation
  埼玉
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Early Repolarizationに関連した特発性心室細動の検討2009
- Author(s)
  八尾武憲, 伊藤誠, et al
- Organizer
  Early Repolarizationに関連した特発性心室細動の検討
- Place of Presentation
  有馬市
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 肺静脈隔離術後の心房細動再発予測におけるエンドセリン1の有用性2009
- Author(s)
  中澤優子, 伊藤誠, et al
- Organizer
  第7回滋賀呼吸循環器フォーラム
- Place of Presentation
  大津市
- Year and Date
  2009-08-29
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Latent genetic backgrounds and molecular pathogenesis of drug-induced long QT syndrome2009
- Author(s)
  Itoh H, Watanabe E, Watanabe I, Sakaguchi T, Makiyama T, Akao M, Oono S, Zenda N, Higashi Y, Mori C, Okajima K, Matsuura H, Horie M
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] 家族性ペースメーカー植込み症例における遺伝的背景の検討-心臓NA+チャネル病、lamin A/C関連心筋症-2009
- Author(s)
  牧山武, 横出正之, 赤尾昌治, 静田聡, 土井孝浩, 池田智之, 大野聖子, 服部哲久, 西尾由貴子, 木村剛, 北徹, 宮本証, 伊藤英樹, 堀江稔
- Organizer
  第24回日本不整脈学会学術大会第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] SCN5A and lamin A/C gene mutations are highly prevalent in patients with familial bradyarrhythmic disorders2009
- Author(s)
  Makiyama T, Itoh H, et al. (13人中9番目)
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Latent genetic backgrounds and molecular pathogenesis of drug-inducedlong QT syndrome.2009
- Author(s)
  Itoh H
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Early Repolarization に関連した特発性心室細動の検討2009
- Author(s)
  八尾武憲, 宮本証, 中津優子, 伊藤英樹, 芦原貴司, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第25回心電情報処理ワークショップ
- Place of Presentation
  有馬
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] A novel genetic marker for potential risk of QT prolongation and cardiac sudden death -KCNE1-D85N polymorphism2009
- Author(s)
  Nishio Y, Itoh H, et al : (9人中2番目)
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 冠動脈洞開口以上を合併した防湿回帰性頻拍にカテ-テル・アブレ-ションを施行し根治しえた1例2009
- Author(s)
  伊藤英樹, 伊藤誠, et al
- Organizer
  第21回カテーテル・アブレーション委員会公開研究会
- Place of Presentation
  さいたま市
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 冠動脈洞開口以上を合併した防湿回帰性頻拍にカテーテル・アブレーションを施行し根治しえた1例2009
- Author(s)
  伊藤英樹, 八尾武憲, 宮本証, 中澤優子, 城日加里, 水澤有香, 芦原貴司, 八木崇文, 横田良司, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第21回カテーテル・アブレーション委員会公開研究会
- Place of Presentation
  埼玉
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Early Repolarizationに関連した特発性心室細動の検討2009
- Author(s)
  八尾武憲, 宮本証, 中津優子, 伊藤英樹, 芦原貴司, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第25回心電情報処理ワークショップ
- Place of Presentation
  有馬
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Severer phenotypes of long QT syndrome are associated with compound mutations : A multicenter study.2009
- Author(s)
  Itoh H
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] 学術諮問委員会指定トピックス先天性QT延長症候群における遺伝子診断-複数変異例の検討-2009
- Author(s)
  伊藤英樹
- Organizer
  第24回日本不整脈学会・第26回日本心電図学会合同学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21790718
[Presentation] 肺静脈隔離術後の心房細動再発検出における携帯型心電計の有用性2009
- Author(s)
  中澤優子, 芦原貴司, 八尾武憲, 城日加里, 伊藤英樹, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第29回日本ホルター・ノンインベイシブ心電学研究会(JASHNE 2009)
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 抗凝固治療法を中心とした心房細動ガイドラインの応用2009
- Author(s)
  伊藤誠
- Organizer
  湖北医師会学術講演会
- Place of Presentation
  滋賀
- Year and Date
  2009-09-24
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 多量の心嚢水貯留を認めた好酸球性心筋炎の一例2009
- Author(s)
  吉井理一郎, 伊藤英樹, 高山幸一郎, 山下寛人, 八尾武憲, 谷口晋, 中澤優子, 芦原貴司, 山本孝, 高島弘行, 藤井応理, 中江一郎, 林秀樹, 杉本喜久, 松本鉄也, 蔦本尚慶, 伊藤誠, 堀江稔
- Organizer
  第67回滋賀県循環器疾患研究会
- Place of Presentation
  滋賀
- Year and Date
  2009-09-12
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] A Novel Gain-of-function KCNJ2 Mutation Associated With Short QT Syndrome Impairs Inward Rectification of Kir 2.1 Currents2009
- Author(s)
  Hattori T, Makiyama T, Akao M, Ehara E, Ohno S, Nishio Y, Itoh H, Yokode M, Kimura T, Horie M
- Organizer
  AHA Scientific Sessions 2009
- Place of Presentation
  Orlando, Florida, U.S.A.
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] 多量の心嚢水貯留を認めた好酸球性心筋炎の一例2009
- Author(s)
  吉井理―郎, 伊藤英樹, 高山幸一郎, 山下寛人, 八尾武憲, 谷口晋, 中澤優子, 芦原貴司, 山本孝, 高島弘行, 藤井応理, 中江一郎, 林秀樹, 杉本喜久, 松本鉄也, 蔦本尚慶, 伊藤誠, 堀江稔
- Organizer
  第67回滋賀県循環器疾患研究会
- Place of Presentation
  滋賀
- Year and Date
  2009-09-12
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] 肺静脈隔離術後の心房細動再発検出における携帯型心電計の有用性2009
- Author(s)
  中澤優子, 伊藤誠, et al
- Organizer
  第29回日本ホルター・ノンインベイシブ心電学研究会
- Place of Presentation
  横浜市
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 多量の心嚢水を認めた好酸球性心筋炎の1例2009
- Author(s)
  吉井理一郎, 伊藤誠, et al
- Organizer
  第189回日本内科学会近畿地方会
- Place of Presentation
  大阪市
- Year and Date
  2009-09-26
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 先天性QT延長症候群の遺伝子診断-複数変異例の検討-2009
- Author(s)
  伊藤英樹, 清水渉, 林研至, 山形研一郎, 坂口知子, 大野聖子, 牧山武, 赤尾昌治, 藍智彦, 野田崇, 宮崎彩, 宮本恵宏, 山岸正和, 鎌倉史郎, 堀江稔
- Organizer
  第24回日本不整脈学会学術大会第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] 心房細動に対するベプリジルの適正使用について2009
- Author(s)
  芦原貴司, 八尾武憲, 森田幸弘, 中澤優子, 城日加里, 伊藤英樹, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第25回滋賀不整脈カンファレンス
- Place of Presentation
  滋賀
- Year and Date
  2009-04-18
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] At-Home AED : ICD植込みが困難な患者に対する代替法としてのAED利用について2009
- Author(s)
  八尾武憲, 伊藤誠, et al
- Organizer
  第24回日本不整脈学会学術大会第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都市
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 肺静脈隔離術後の心房細動再発予測におけるエンドセリン1の有用性2009
- Author(s)
  中澤優子, 芦原貴司, 八尾武憲, 伊藤英樹, 城日加里, 杉本喜久, 蔦本尚慶, 伊藤誠, 堀江稔, 八木崇文
- Organizer
  第7回滋賀呼吸循環器フォーラム
- Place of Presentation
  大津
- Year and Date
  2009-08-29
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] 心房細動に対するベプリジルの適正使用について2009
- Author(s)
  芦原貴司, 伊藤誠, et al
- Organizer
  第25回滋賀不整脈カンファレンス
- Place of Presentation
  滋賀県
- Year and Date
  2009-04-18
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 多量の心嚢水を認めた好酸球性心筋炎の1例2009
- Author(s)
  吉井理一郎, 高山幸一郎, 山下寛人, 中澤優子, 伊藤英樹, 高島弘行, 伊藤誠, 堀江稔
- Organizer
  第189回日本内科学会近畿地方会
- Place of Presentation
  大阪
- Year and Date
  2009-09-26
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] 多量の心嚢水を認めた好酸球性心筋炎の1例2009
- Author(s)
  吉井理一郎, 高山幸一郎, 山下寛人, 中澤優子, 伊藤英樹, 高島弘行, 伊藤誠, 堀江稔
- Organizer
  第189回日本内科学会近畿地方会
- Place of Presentation
  大阪
- Year and Date
  2009-09-26
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Event ECG recording is useful tool for atrial fibrillation (AF) recurrence after pulmonary vein isolation (PVI)2009
- Author(s)
  Ito M, Itoh H, et al. (8人中6番目)
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] At-Home AED : ICD植込みが困難な患者に対する代替法としてのAED利用について2009
- Author(s)
  八尾武憲, 城日加里, 中澤優子, 伊藤英樹, 芦原貴司, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第24回日本不整脈学会学術大会第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] ARBと不整脈2009
- Author(s)
  伊藤誠
- Organizer
  REGESSION SUMMIT in滋賀Metabolic & CV
- Place of Presentation
  滋賀
- Year and Date
  2009-09-26
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] At-Home AED : ICD植込みが困難な患者に対する代替法としてのAED利用について2009
- Author(s)
  八尾武憲, 城日加里, 中澤優子, 伊藤英樹, 芦原貴司, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第24回日本不整脈学会学術大会第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Overlap between LQT3 and syndrome : Clinical features in a common mutation and underlying biophysical mechanisms2009
- Author(s)
  Makita N, Shimizu W, Miyamoto K, Kamakura S, Horie M, Itoh H, Crotti L, Schwartz PJ, George AL Jr, Roden DM
- Organizer
  第24回日本不整脈学会学術大会第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Event ECG recording is useful tool for atrial fibrillation (AF) recurrence after pulmonary vein isolation (PVI)2009
- Author(s)
  Ito M, Nakazawa Y, Yao T, Ashihara T, Joh H, Itoh H, Sugimoto Y, Horie M
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] ICD植え込み後にVF onset が明らかとなった心肺蘇生後の一例2009
- Author(s)
  八尾武憲, 宮本証, 中澤優子, 伊藤英樹, 芦原貴司, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  ICD公開研究会学術集会
- Place of Presentation
  大阪
- Year and Date
  2009-12-19
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Severer phenotypes of long QT syndrome are associated with cornpound mutations : A multicenter study2009
- Author(s)
  Itoh H
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 肺静脈隔離術後の心房細動再発予測におけるエンドセリン1の有用性2009
- Author(s)
  中澤優子, 芦原貴司, 八尾武憲, 伊藤英樹, 城日加里, 杉本喜久, 蔦本尚慶, 伊藤誠, 堀江稔, 八木崇文
- Organizer
  第7回滋賀呼吸循環器フォーラム
- Place of Presentation
  大津
- Year and Date
  2009-08-29
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Severer phenotypes of long QT syndrome are associated with compound mutations : A multicenter study2009
- Author(s)
  Itoh H, et al. (11人中1番目)
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 肺静脈隔離術後の心房細動再発検出における携帯型心電計の有用性2009
- Author(s)
  中澤優子, 芦原貴司, 八尾武憲, 城日加里, 伊藤英樹, 杉本喜久, 伊藤誠, 堀江稔
- Organizer
  第29回日本ホルター・ノンインベイシブ心電学研究会 (JASHNE 2009)
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] ARBと不整脈. REGESSION SUMMIT in滋賀Metabolic & CV2009
- Author(s)
  伊藤誠
- Organizer
  REGESSION SUMMIT in滋賀Metabolic & CV
- Place of Presentation
  大津市
- Year and Date
  2009-09-26
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] 冠動脈洞開口異常を合併した房室回帰性頻拍にカテーテル・アブレーションを施行し根治しえた1例2009
- Author(s)
  伊藤英樹
- Organizer
  第189回日本内科学会近畿地方会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21790718
[Presentation] 多種類の上室頻拍を合併した心臓手術後の一例2009
- Author(s)
  城日加里, 伊藤誠, et al.
- Organizer
  第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都市
- Data Source
  KAKENHI-PROJECT-21590891
[Presentation] Severer phenotypes of long QT syndrome are associated with compound mutations: A multicenter study2009
- Author(s)
  Itoh H, Shimizu W, Yamagata K, Sakaguchi T, Oono S, Makiyama T, Akao M, Noda T, Miyamoto Y, Kamakura S, Horie M
- Organizer
  第73回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Brugada Syndrome and Diverse Phenotypes of Cardiac Sodium Channelopathies2008
- Author(s)
  Makiyama T, Itoh H, et al. (10人中8番目)
- Organizer
  第72回日本循環器学会・学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Overlap Between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms2008
- Author(s)
  Makita N, Itoh H, et al. (6人中4番目)
- Organizer
  第72回日本循環器学会・学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 薬剤誘発性QT延長症例の原因薬剤と遺伝子異常同定率2008
- Author(s)
  伊藤英樹
- Organizer
  第23回日本不整脈学会学術大会
- Place of Presentation
  神奈川
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Molecular Pathogenesis of Genotyped Drug-lnduced Long QT Syndrome2008
- Author(s)
  Itoh H
- Organizer
  第72回日本循環器学会・学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] A Common KCNE1 Polymorphism, D85N, is a Genetic Modifier of Long QT Syndrome2008
- Author(s)
  Nishio Y, Itoh H, et al. (10人中5番目)
- Organizer
  第72回日本循環器学会・学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 軟球が左胸部を直撃後、埋め込み型除細動器が頻回誤作動した一例2008
- Author(s)
  伊藤英樹, 他 (9人中1番目)
- Organizer
  第106回日本循環器学会近畿地方会
- Place of Presentation
  兵庫
- Year and Date
  2008-11-29
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Brugada症候群、Brugada様心電図患者におけるSCN5A遺伝子解析2008
- Author(s)
  牧山武, 伊藤英樹, 他. (9人中7番目)
- Organizer
  第25回日本心電学会学術集会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] SCN5Aのgain-of-functionによる家族性心房細動の発症メカニズムに関する数値解析的研究2008
- Author(s)
  芦原貴司, 伊藤英樹, 他. (10人中6番目)
- Organizer
  第24回心電情報処理ワークショップ
- Place of Presentation
  神奈川
- Year and Date
  2008-10-18
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 家族性ペースメーカー植え込み症例の遺伝子解析2008
- Author(s)
  宮本証、伊藤英樹, 他. (12人中2番目)
- Organizer
  第6回滋賀呼吸循環器フォーラム
- Place of Presentation
  滋賀
- Year and Date
  2008-07-12
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] SCN5Aの遺伝子異常(R179X)を有した下壁誘導ST上昇型Brugada症候群の1例2008
- Author(s)
  川村美朋子, 伊藤英樹, 他. (10人中5番目)
- Organizer
  第23回日本不整脈学会学術大会
- Place of Presentation
  神奈川
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 全国登録データを生かすには?2008
- Author(s)
  伊藤英樹, 他. (4人中1番目)
- Organizer
  平成19年度厚生労働科学研究費補助金創薬基盤推進研究事業「致死性遺伝性不整脈疾患の遺伝子診断と臨床応用」班会議
- Place of Presentation
  大阪
- Year and Date
  2008-01-29
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Cardiac sodium channel gene mutations are prevalent in Japanese patients with familial sick sinus syndrome2008
- Author(s)
  Makiyama T, Itoh H, et al. (9人中7番目)
- Organizer
  第72回日本循環器学会・学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 軟球が左胸部を直撃後、埋め込み型除細動器が頻回誤作動した-例2008
- Author(s)
  伊藤英樹
- Organizer
  第106回日本循環器学会近畿地方会
- Place of Presentation
  兵庫
- Year and Date
  2008-11-29
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 本邦におけるQT延長症候群の遺伝的背景 : 先天性と後天性における相違2008
- Author(s)
  伊藤英樹, 他. (10人中1番目)
- Organizer
  第105回日本内科学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 薬剤誘発性QT延長症例の原因薬剤と遺伝子異常同定率2008
- Author(s)
  伊藤英樹, 他. (13人中1番目)
- Organizer
  第23回日本不整脈学会学術大会
- Place of Presentation
  神奈川
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 薬剤誘発性QT延長症例の原因薬剤と遺伝子異常同定率2008
- Author(s)
  伊藤英樹
- Organizer
  第23回日本不整脈学会学術大会
- Place of Presentation
  神奈川
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] SCN5Aのgain-of-functionによる家族性心房細動の発症メカニズム : コンピュータシミュレーションによる検討2008
- Author(s)
  芦原貴司, 伊藤英樹, 他. (10人中6番目)
- Organizer
  第25回日本心電学会学術集会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Molecular Pathogenesis of Genotyped Drug-Induced Long QT Syndrome.2008
- Author(s)
  Itoh H
- Organizer
  第72回日本循環器学会・学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 全国登録データを生かすには?.2008
- Author(s)
  伊藤英樹
- Organizer
  平成19年度厚生労働科学研究費補助金創薬基盤推進研究事業「致死性遺伝性不整脈疾患の遺伝子診断と臨床応用」班会議
- Place of Presentation
  大阪
- Year and Date
  2008-01-29
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 房室ブロックによる後天性QT延長症候群の遺伝学的背景とその臨床像2008
- Author(s)
  岡優子, 伊藤英樹, 他. (9人中2番目)
- Organizer
  第23回日本不整脈学会学術大会
- Place of Presentation
  神奈川
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation2008
- Author(s)
  Makiyama T, Itoh H, et al. (13人中10番目)
- Organizer
  第72回日本循環器学会・学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Mutation analysis for the human cariac ryanodine receptor gene (RyR2) in catecholaminergic polymorphic ventricular tachycardia (CPVT)2007
- Author(s)
  Nagaoka I, Itoh H, et al. (11人中2番目)
- Organizer
  The 71st Annual Scientific Meeting of Japanese Circulation Society
- Place of Presentation
  Kobe, Japan
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 先天性2型QT延長症候群の不整脈発症リスク評価 : 遺伝子検索から臨床へ2007
- Author(s)
  長岡伊織, 伊藤英樹, 他. (10人中2番目)
- Organizer
  第12回京滋不整脈研究会
- Place of Presentation
  京都
- Year and Date
  2007-10-13
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 家庭用心電計の評価と適性使用に関する小委員会報告:家庭用心電計の使用経験2007
- Author(s)
  伊藤誠
- Organizer
  第24回日本心電図学会学術集会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms2007
- Author(s)
  Makita N, Behr E, Shimizu W, Horie M, Crotti L, Itoh H, Miyamoto K, Kamakura S, Tsutsui H, Schwartz PJ, George AL Jr, Roden DM.Overlap Between LQT3, Brugada Syndrome:
- Organizer
  The American Heart Association Scientific Sessions 2007
- Place of Presentation
  U.S. A
- Year and Date
  2007-11-05
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Overlap Between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms2007
- Author(s)
  Makita N, Itoh H, et al. (12人中6番目)
- Organizer
  The American Heart Association Scientific Sessions 2007
- Place of Presentation
  U. S. A.
- Year and Date
  2007-11-05
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Variable genetic backgrounds between congenital and acquired long-QT syndromes2007
- Author(s)
  Itoh H, et al. (13人中1番目)
- Organizer
  The 71st Annual Scientific Meeting of Japanese Circulation Society
- Place of Presentation
  Kobe, Japan
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 心筋Naチャネルの遺伝子異常と薬剤誘発性不整脈2007
- Author(s)
  蒔田直昌, 伊藤英樹, 他 (8人中6番目)
- Organizer
  第24回日本心電学会学術集会
- Place of Presentation
  愛知
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 遺伝性不整脈について2007
- Author(s)
  伊藤英樹
- Organizer
  滋賀医科大学メディカルグランドラウンド
- Place of Presentation
  滋賀
- Year and Date
  2007-12-12
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] A novel KCNH2 mutation associated with the short QT interval of Brugada syndrome. Impaired deactivation for the Ikr channel(Poster).2007
- Author(s)
  Itoh H, et al. (11人中1番目)
- Organizer
  56th Annual Scientific Session of the American College of Cardiology (ACC)
- Place of Presentation
  New Orleans, U. S. A.
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Age-Related Triggers for Life-Threatning Arrhythmia in the Genotyped Long QT Syndrome2007
- Author(s)
  Sakaguchi T, Itoh H, et al. (13人中3番目)
- Organizer
  The American Heart Association Scientific Sessions 2007
- Place of Presentation
  U. S. A.
- Year and Date
  2007-11-06
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 家族性洞不全症候群の1家系に認めた心臓Naチャネル(SCN5A)遺伝子異常の電気生理学的機能解析2007
- Author(s)
  牧山武, 伊藤英樹, 他. (9人中7番目)
- Organizer
  第24回日本心電学会学術集会
- Place of Presentation
  愛知
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 心外膜側からパーフェクトマップが得られたにもかかわらず、心内膜側からの通電にて焼灼しえた左室流出路起源心室頻拍の一例2007
- Author(s)
  伊藤英樹, 他 (6人中1番目)
- Organizer
  第18回滋賀不整脈研究会
- Place of Presentation
  大津
- Year and Date
  2007-02-03
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 遺伝性不整脈疾患の分子病態2007
- Author(s)
  伊藤英樹
- Organizer
  第4回 CEMフォーラム
- Place of Presentation
  京都
- Year and Date
  2007-03-24
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] QT延長症候群の遺伝的背景〜先天性と後天性の比較検討2007
- Author(s)
  伊藤英樹
- Organizer
  第27回近畿循環器疾患治療研究会
- Place of Presentation
  大阪
- Year and Date
  2007-08-25
- Data Source
  KAKENHI-PROJECT-19390212
[Presentation] Variable genetic backgrounds between congenital and acquired long-QT syndromes2007
- Author(s)
  Itoh H, et al. (10人中1番目)
- Organizer
  56th Annual Scientific Session of the American College of Cardiology (ACC)
- Place of Presentation
  New Orleans, U. S. A.
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 不整脈の基礎と臨床〜遺伝子からカテーテル治療まで〜2007
- Author(s)
  伊藤英樹
- Organizer
  レクチャーミーティング
- Place of Presentation
  滋賀
- Year and Date
  2007-06-26
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Clinical characteristics for Japanese patients with genotyped long-QT syndrome(Poster)2007
- Author(s)
  Oka Y, Itoh H, et al. (10人中3番目)
- Organizer
  The 71st Annual Scientific Meeting of Japanese Circulation Society
- Place of Presentation
  Kobe, Japan
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 遺伝子変異を認めた薬剤性QT延長症候群の一症例-KCNH2遺伝子変異(A614V)と第一世代抗ヒスタミン薬ヒドロキシジン(アタラックスP)-2007
- Author(s)
  坂口知子, 伊藤英樹, 他(17人中2番目)
- Organizer
  第18回滋賀不整脈研究会
- Place of Presentation
  大津
- Year and Date
  2007-02-03
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] QT延長症候群の遺伝的背景〜先天性と後天性の比較検討2007
- Author(s)
  伊藤英樹, 他 (10人中1番目)
- Organizer
  第27回近畿循環器疾患治療研究会
- Place of Presentation
  大阪
- Year and Date
  2007-08-25
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 先天性QT延長症候群1型および2型における心イベント発症リスクの評価-不整脈関連遺伝子検索から臨床へのfeedback2006
- Author(s)
  長岡伊織, 伊藤英樹, 他. (14人中2番目)
- Organizer
  第4回滋賀呼吸循環器フォーラム
- Place of Presentation
  大津
- Year and Date
  2006-07-22
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] KCNH2遺伝子変異(S641F)を認めたQT延長症候群の臨床および電気生理学的特徴2006
- Author(s)
  坂口知子, 伊藤英樹, 他. (17人中2番目)
- Organizer
  第21回日本不整脈学会学術大会(JHRS)/第23回日本心電学会学術集会(JSE)
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 心筋リアノジン受容体(hRYR2)の遺伝子変異を有したカテコラミン誘発性多形性心室頻拍(CPVT)の2症例2006
- Author(s)
  道智賢市, 伊藤英樹, 他. (13人中8番目)
- Organizer
  第102回日本循環器学会近畿地方会
- Place of Presentation
  大津
- Year and Date
  2006-12-09
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] 心筋Naチャネルの抗不整脈薬結合関連部位に遺伝子異変を認めたBrugada症候群における薬剤負荷試験と抗不整脈薬治療2006
- Author(s)
  伊藤英樹, 他 (7人中1番目)
- Organizer
  第3回不整脈薬物治療フォーラム
- Place of Presentation
  東京
- Year and Date
  2006-04-22
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] Long QT syndrome : an ion channelopathy in cardiovasccular medicine2006
- Author(s)
  Horie M, Itoh H, et al. (14人中2番目)
- Organizer
  The 11th La Jolla-Capri-Yamaguchi-Seoul Research Conference
- Place of Presentation
  Yamaguchi
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] QT短縮を認めたBrugada症候群における新たなKCNH2遺伝子変異2006
- Author(s)
  伊藤英樹, 他. (12人中1番目)
- Organizer
  循環病研究委託事業 16 公-3 班会議「無症候性Brugada症候群の予後に関する研究(多施設共同継続研究)
- Place of Presentation
  大阪
- Year and Date
  2006-12-09
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] RAA型と心筋イオンチャネル2006
- Author(s)
  伊藤英樹, 他 (11人中1番目)
- Organizer
  第4回滋賀心血管とリスクファクター研究会
- Place of Presentation
  大津
- Year and Date
  2006-10-21
- Data Source
  KAKENHI-PROJECT-18790496
[Presentation] The Prognosis of Andersen-Tawil syndrome is not so benign as ever thought
- Author(s)
  Kimura H, Itoh H, Ohno S, Fukuyama M, Kato K, Ichikawa M, Fujii Y, Makiyama T, Horie M
- Organizer
  AHA Scientific Sessions 2014
- Place of Presentation
  Chicago,アメリカ合衆国
- Year and Date
  2014-11-15 – 2014-11-19
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Acquired long QT syndrome.
- Author(s)
  Itoh H.
- Organizer
  7th APHRS 2014
- Place of Presentation
  New Delhi,インド
- Year and Date
  2014-10-29 – 2014-11-01
- Invited
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Identification of novel SCN10A variants in Brugada syndrome patients.
- Author(s)
  Fukuyama M, Ohno S, Makiyama T, Hasegawa K, Itoh H, Horie M.
- Organizer
  ESC CONGRESS 2014
- Place of Presentation
  Barcelona,スペイン
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Identification of latent mutations in primary inherited arrhythmia syndromes using benchtop next generation sequencer.
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M.
- Organizer
  ESC CONGRESS 2014
- Place of Presentation
  Barcelona,スペイン
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] The genetics underlying the acquired long QT syndrome. Impact on management
- Author(s)
  Itoh H, Spazzolini C, Crotti L, Aiba T, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M
- Organizer
  Heart Rhythm Society’s 36th Annual Scientific Sessions
- Place of Presentation
  Boston,アメリカ合衆国
- Year and Date
  2015-05-13 – 2015-05-15
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Genetics in acquired long QT syndrome
- Author(s)
  Pedrazzini M, Itoh H, Crotti L, Aiba T, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Yamagishi M, Berthet M, Shimizu W, Guicheney P, Schwartz PJ, Horie M
- Organizer
  ESHG 2014
- Place of Presentation
  Milano,イタリア共和国
- Year and Date
  2014-05-31 – 2014-06-03
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Mosaic KCNJ2 Mutation in Andersen-Tawil syndrome:Targeted Deep Sequencing is Useful for the Detection of Mosaicism
- Author(s)
  Hasegawa K,Ohno S,Kimura H,Itoh H,Makiyama T,Yoshida Y,Horie M
- Organizer
  Heart Rhythm2014
- Place of Presentation
  San Francisco,アメリカ合衆国
- Year and Date
  2014-05-06 – 2014-05-11
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Usefulness of Benchtop Next Generation Sequencer in Research of Inherited Primary Arrhythmia Syndromes
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M
- Organizer
  The 79th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Osaka
- Year and Date
  2015-04-24 – 2015-04-26
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Young long QT syndrome patients with KCNH2 mutations have late onset but severe symptoms
- Author(s)
  Ozawa J, Ohno S, Itoh H, Makiyama T, Horie M
- Organizer
  AHA Scientific Sessions 2014
- Place of Presentation
  Chicago,アメリカ合衆国
- Year and Date
  2014-11-15 – 2014-11-19
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Young long QT syndrome patients with KCNH2 mutations have late onset but severe symptoms.
- Author(s)
  Ozawa J, Ohno S, Itoh H, Makiyama T, Horie M.
- Organizer
  AHA Scientific Sessions 2014
- Place of Presentation
  Chicago,アメリカ合衆国
- Year and Date
  2014-11-15 – 2014-11-19
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Usefulness of Benchtop Next Generation Sequencer in Research of Inherited Primary Arrhythmia Syndromes.
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M.
- Organizer
  The 79th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Osaka
- Year and Date
  2015-04-24 – 2015-04-26
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] High frequency of ANK2 mutations in patients with non-genotyped primary inherited arrhythmia syndromes
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M
- Organizer
  ESC CONGRESS 2014
- Place of Presentation
  Barcelona,スペイン
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Genetics in acquired long QT syndrome.
- Author(s)
  Pedrazzini M, Itoh H, Crotti L, Aiba T, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Yamagishi M, Berthet M, Shimizu W, Guicheney P, Schwartz PJ, Horie M.
- Organizer
  ESHG 2014
- Place of Presentation
  Milano,イタリア共和国
- Year and Date
  2014-05-31 – 2014-06-03
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] High frequency of ANK2 mutations in patients with non-genotyped primary inherited arrhythmia syndromes.
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M.
- Organizer
  ESC CONGRESS 2014
- Place of Presentation
  Barcelona,スペイン
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Identification of latent mutations in primary inherited arrhythmia syndromes using benchtop next generation sequencer
- Author(s)
  Ohno S, Fukuyama M, Itoh H, Makiyama T, Horie M
- Organizer
  ESC CONGRESS 2014
- Place of Presentation
  Barcelona,スペイン
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Acquired long QT syndrome
- Author(s)
  Itoh H
- Organizer
  7th APHRS 2014
- Place of Presentation
  New Delhi,インド
- Year and Date
  2014-10-29 – 2014-11-01
- Invited
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] Identification of novel SCN10A variants in Brugada syndrome patients
- Author(s)
  Fukuyama M, Ohno S, Makiyama T, Hasegawa K, Itoh H, Horie M
- Organizer
  ESC CONGRESS 2014
- Place of Presentation
  Barcelona,スペイン
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PUBLICLY-25136705
[Presentation] The Prognosis of Andersen-Tawil syndrome is not so benign as ever thought
- Author(s)
  Kimura H, Itoh H, Ohno S, Fukuyama M, Kato K, Ichikawa M, Fujii Y, Makiyama T, Horie M.
- Organizer
  AHA Scientific Sessions 2014
- Place of Presentation
  Chicago,アメリカ合衆国
- Year and Date
  2014-11-15 – 2014-11-19
- Data Source
  KAKENHI-PROJECT-25460406
[Presentation] Mosaic KCNJ2 Mutation in Andersen-Tawil syndrome:Targeted Deep Sequencing is Useful for the Detection of Mosaicism
- Author(s)
  Hasegawa K,Ohno S,Kimura H,Itoh H,Makiyama T,Yoshida Y,Horie M.
- Organizer
  Heart Rhythm2014
- Place of Presentation
  San Francisco, アメリカ合衆国
- Year and Date
  2014-05-06 – 2014-05-11
- Data Source
  KAKENHI-PROJECT-25460406

1. HORIE Minoru (90183938)

# of Collaborated Projects: 6 results

# of Collaborated Products: 135 results
2. ASHIHARA Takashi (80396259)

# of Collaborated Projects: 3 results

# of Collaborated Products: 19 results
3. 大野聖子 (20610025)

# of Collaborated Projects: 2 results

# of Collaborated Products: 25 results
4. TSUJI Keiko (70432309)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
5. ITO Makoto (70159911)

# of Collaborated Projects: 1 results

# of Collaborated Products: 40 results
6. OZAWA Tomoya (20584395)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
7. NAKAZAWA Yuko (90564914)

# of Collaborated Projects: 1 results

# of Collaborated Products: 16 results
8. YAO Takenori (90402726)

# of Collaborated Projects: 1 results

# of Collaborated Products: 18 results
9. WU Jie (40595097)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. 牧山武 (30528302)

# of Collaborated Projects: 1 results

# of Collaborated Products: 13 results
11. 林秀樹 (70464188)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
12. 松浦博 (60238962)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
13. 竹島浩 (70212024)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
14. 加藤浩一 (70736983)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
15. TAKAHASHI Masanori

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
16. AIBA Takeshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
17. UESHIMA satoshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. 豊田太

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
19. 丁維光

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
20. 平大樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
21. 福山恵

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
22. 蒔田直昌

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
23. 国広なごみ

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 村山尚

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 南野徹

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 竹内綾子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 松岡達

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 桂敏也

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Itoh Hideki 伊藤 英樹

ITOH Hideki 伊藤 英樹

Research Projects

Research Products

Co-Researchers

The genetic analysis and underlying function of the endoplasmic reticulum membrane protein targeting inherited arrhythmogenic syndromesPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

The risk stratification of drug-induced long QT syndrome upon the underlying geneticsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Multilateral Research on the Mechanisms of Inherited Arrhythmias

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

心筋イオンチャネル病のリスク層別化と臨床管理におけるシミュレーションの応用Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Genetic epidemiology in the ion channel diseasePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Multidisciplinary Studies on Molecular Pathogenesis of Inherited Primary Arrhythmia Syndromes

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Evaluation of Efficacy and Long-term Results of Catheter Ablation in Drug-refractory Atrial Fibrillation

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

潜在性突然死症候群の顕在化に関与する遺伝的背景と分子病態の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Genotype-phenotype relation study on inherited cardiac arrhythmias as ion hcannel diseases

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Genetic Backgrounds and Functional Analysis in SCN5A Mutation-Negative Brugada SyndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] Management of Cardiac Arrhythmias, 3rd ed. Chapter 20 Acquired Long QT Syndrome and Torsades de Pointes2020

Author(s)

Publisher

Data Source

[Book] Management of Cardiac Arrhythmias,3rd ed.2020

Author(s)

Total Pages

Publisher

Data Source

[Book] 不整脈薬物治療ガイドライン2020年改訂版2020

Author(s)

Total Pages

Publisher

Data Source

[Book] 循環器疾患最新の治療2018-20192018

Itoh Hideki 伊藤英樹

ITOH Hideki 伊藤英樹

[Book] 見逃すな！薬物中毒と電解質異常. レジデントノート　心電図の読み方トレニーング2013

[Book] 見逃すな！薬物中毒と電解質異常. レジデントノート　心電図の読み方トレニーング2013