HIRANO Makito 平野牧人

… Alternative Names

平野政人ヒラノマサト

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Researcher Number	50347548
Other IDs
Affiliation (Current)	2025: 近畿大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2021 – 2024: 近畿大学, 医学部, 教授 2017 – 2021: 近畿大学, 医学部, 准教授 2010 – 2016: 近畿大学, 医学部附属病院, 准教授 2014: 近畿大学, 医学部・附属病院, 准教授 2011: 近畿大学, 医学部・附属病院, 准教授 … More 2010: 近畿大学, 医学部付属病院, 准教授 2007 – 2009: Nara Medical University, 医学部, 准教授 2002 – 2004: 奈良県立医科大学, 医学部, 講師 2003: 奈良県立医科大学, 医学部, 助手 Less
Review Section/Research Field	Principal Investigator Neurology / Basic Section 52020:Neurology-related Except Principal Investigator Neurology / Medium-sized Section 59:Sports sciences, physical education, health sciences, and related fields / Neurology
Keywords	Principal Investigator 筋萎縮性側索硬化症 / iPS細胞 / SCA8 / 運動ニューロン / ALS / アプラタキシン / 小脳失調症 / 治療法開発 / 病態解明 / リピート病 … More / 核酸治療薬 / iPS / 非翻訳領域反復配列 / ATXN8 / ATXN8OS / 非翻訳領域反復配列延長 / 核酸医薬品 / 脳神経疾患 / 抗がん剤 / 治療薬開発 / ERBB4 / リン酸化阻害剤 / ubiquiliin2 / 人工多能性幹細胞 / 神経細胞 / オートファジー / p62 / 翻訳後修復 / 細胞内局在 / 蛋白相互作用 / 神経変性疾患 / 翻訳後修飾 / 核内輸送 / XRCC1 / アラジン / 臨床神経分子遺伝学 / スプライス変異体 … More Except Principal Investigator 深部脳 / 嚥下 / 歩行 / 神経可塑性 / mitochondrial disease / apoptosis / Humanin / 神経細胞死 / ヒューマン / ミトコンドリア病 / ミトコンドリア脳筋症 / アポトーシス / ヒューマニン / 自己抗体 / ミエリン / シアル酸 / ギラン・バレー症候群 / 脱髄 / 硫酸化糖脂質 / ガングリオシド / 糖脂質 / 神経疾患 / 自己免疫 / 糖鎖 / Parkin / 中心体 / 酸化的ストレス / 神経変性疾患 / DNA修復 / 臨床神経分子遺伝学 Less

クローズドループ刺激による非侵襲的Deep Brainリハビリテーションの創生
- Principal Investigator
  
  美馬達哉
- Project Period (FY)
  2023 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 59:Sports sciences, physical education, health sciences, and related fields
- Research Institution
  Ritsumeikan University
The clarification of pathomechanism and the establishment of treatment for repeat expansion-associated amyotrophic lateral sclerosisPrincipal Investigator
- Principal Investigator
  
  平野牧人
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Kindai University
Identification of proteins associated with ATXN8OS-related amyotrophic lateral sclerosis and treatment of iPS cell modelsPrincipal Investigator
- Principal Investigator
  
  Hirano Makito
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Kindai University
Clarification of pathomechanism via amyotrophic lateral sclerosis-causing ERBB4 and effectiveness of anti-cancer medicine.Principal Investigator
- Principal Investigator
  
  HIRANO Makito
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kindai University
Therapeutic protein degradation and relationship between p62 and ubiquilin 2, new proteins causative for neurodegenerative diseasesPrincipal Investigator
- Principal Investigator
  
  HIRANO Makito
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kinki University
Analysis of negative regulators of B lymphocyte responses to glycoconjugates in neuroimmunological diseases
- Principal Investigator
  
  KUSUNOKI Susumu
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Neurology
- Research Institution
  Kinki University
Interaction, posttranslational modification, and subcellular localization of proteins causative for neurodegenerative diseasesPrincipal Investigator
- Principal Investigator
  
  HIRANO Makito
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kinki University
  Nara Medical University
Repairing DNA damages in neurodegenerative diseases
- Principal Investigator
  
  UENO Satoshi
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Nara Medical University
Clarification of the link between nuclear import of neurodegenerative disease-causing proteins and the pathomechanismsPrincipal Investigator
- Principal Investigator
  
  HIRANO Makito
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Nara Medical University
遺伝性小脳失調原因遺伝子アプラタキシンの野生型及びスプライス変異型蛋白の機能解析Principal Investigator
- Principal Investigator
  
  平野牧人
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neurology
- Research Institution
  Nara Medical University
Analyses for the function and related gene of humanin that suppresses cell death induced by mutant Alzheimer disease genes
- Principal Investigator
  
  UENO Satoshi
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Nara Medical University

[Book] 脳神経内科疾患の摂食嚥下・栄養ケアハンドブック患者・家族とケアスタッフのための手引きとQ＆A2023
- Author(s)
  平野牧人　他　日本神経摂食嚥下・栄養学会会員
- Total Pages
  168
- Publisher
  医歯薬出版
- ISBN
  4263266749
- Data Source
  KAKENHI-PROJECT-22K07510
[Book] 脳神経内科の摂食嚥下障害2018
- Author(s)
  平野牧人
- Total Pages
  155
- Publisher
  全日本病院出版会
- ISBN
  9784865192537
- Data Source
  KAKENHI-PROJECT-16K09705
[Book] Annual Review神経20182018
- Author(s)
  平野牧人
- Total Pages
  333
- Publisher
  中外出版
- ISBN
  9784498328068
- Data Source
  KAKENHI-PROJECT-16K09705
[Book] Bardet-Biedl(バルデー・ビードル)症候群(pp495-497)　神経症候群IV2014
- Author(s)
  平野牧人
- Total Pages
  835
- Publisher
  日本臨床社
- Data Source
  KAKENHI-PROJECT-25461297
[Book] 医学大辞典2014
- Author(s)
  平野牧人、楠　進
- Publisher
  南山堂
- Data Source
  KAKENHI-PROJECT-25461297
[Book] 医療の最先端-奈良医大からの発信-2008
- Author(s)
  平野牧人, 他42名
- Total Pages
  208
- Publisher
  創元社
- Data Source
  KAKENHI-PROJECT-19591002
[Book] 医療の最先端-奈良医大からの発信-2008
- Author(s)
  上野聡, 平野牧人, 他41名
- Total Pages
  208
- Publisher
  創元社
- Data Source
  KAKENHI-PROJECT-20591008
[Book] ケアマネジメント用語辞典2007
- Author(s)
  平野牧人, 他101名
- Total Pages
  545
- Publisher
  ミネルヴァ書房
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy2023
- Author(s)
  Hirano Makito、Kuwahara Motoi、Yamagishi Yuko、Samukawa Makoto、Fujii Kanako、Yamashita Shoko、Ando Masahiro、Oka Nobuyuki、Nagano Mamoru、Matsui Taro、Takeuchi Toshihide、Saigoh Kazumasa、Kusunoki Susumu、Takashima Hiroshi、Nagai Yoshitaka
- Journal Title
  
  Scientific Reports
  
  Volume: 13 Issue: 1 Pages: 17801-17801
- DOI
  10.1038/s41598-023-45011-8
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K07510, KAKENHI-PROJECT-21H02842
[Journal Article] Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases2022
- Author(s)
  Oda Ituki、Danno Daisuke、Saigoh Kazumasa、Wolf Johanna、Kawashita Norihito、Hirano Makito、Samukawa Makoto、Kitamura Shigekazu、Kikui Shoji、Takeshima Takao、Mitsui Yoshiyuki、Kusunoki Susumu、Nagai Yoshitaka
- Journal Title
  
  Neuroscience Research
  
  Volume: 180 Pages: 83-89
- DOI
  10.1016/j.neures.2022.03.002
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K07510
[Journal Article] Identification of a novel mutation and genotype-phenotype relationship in MEGF10 myopathy2022
- Author(s)
  Fujii Kanako、Hirano Makito、Terayama Atsushi、Inada Rino、Saito Yoshihiko、Nishino Ichizo、Nagai Yoshitaka
- Journal Title
  
  Neuromuscular Disorders
  
  Volume: - Issue: 5 Pages: 436-440
- DOI
  10.1016/j.nmd.2022.01.009
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K07984, KAKENHI-PROJECT-22K07510
[Journal Article] Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan2021
- Author(s)
  Inada R, Hirano M, Oka N, Samukawa M, Saigoh K, Suzuki H, Udaka F, Hashiguchi A, Takashima H, Hamada Y, Nakamura Y, Kusunoki S.
- Journal Title
  
  J Neurol.
  
  Volume: Feb 24 Issue: 8 Pages: 2933-2942
- DOI
  10.1007/s00415-021-10467-z
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18H02742, KAKENHI-PROJECT-19K07984
[Journal Article] Rasagiline monotherapy improves swallowing in patients with Parkinson's disease2020
- Author(s)
  Hirano Makito、Isono Chiharu、Samukawa Makoto、Fukuda Kanji、Kusunoki Susumu
- Journal Title
  
  Parkinsonism & Related Disorders
  
  Volume: 78 Pages: 98-99
- DOI
  10.1016/j.parkreldis.2020.07.010
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K07984
[Journal Article] Pathological Findings in Male Patients With Anti-N-methyl-d-Aspartate Receptor Encephalitis2019
- Author(s)
  Hirano M1,2, Itoh T3, Fujimura H4, Inoue K4, Samukawa M1,2, Nose K5, Sakamoto H2, Maekura S6, Ueno S1,2, Satou T3, Nishioka T4, Kusunoki S, Nakamura Y
- Journal Title
  
  J Neuropathol Exp Neurol
  
  Volume: - Issue: 8 Pages: 735-741
- DOI
  10.1093/jnen/nlz052
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K07984, KAKENHI-PROJECT-17K01486
[Journal Article] Effects of the rotigotine transdermal patch versus oral levodopa on swallowing in patients with Parkinson's disease2019
- Author(s)
  Hirano M, Isono C, Fukuda K, Ueno S, Nakamura Y, Kusunoki S
- Journal Title
  
  J Neurol Sci
  
  Volume: - Pages: 5-10
- DOI
  10.1016/j.jns.2019.07.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K07984
[Journal Article] 脊髄小脳変性症の遺伝子診断と近畿圏における病型2019
- Author(s)
  仲間美奈、西郷和真、平野牧人、濱田征宏、金城ちなつ、寒川　真、長谷川隆典、北口正孝、三井良之、巽　順子、田村和朗、楠　進
- Journal Title
  
  日本カウンセリング学会誌
  
  Volume: 40 Pages: 95-100
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K07984
[Journal Article] PSP-Phenotype in SCA8: Case Report and Systemic Review2019
- Author(s)
  Samukawa M, Hirano M, Saigoh K, Kawai S, Hamada Y, Takahashi D, Nakamura Y, Kusunoki S.
- Journal Title
  
  Cerebellum
  
  Volume: 18 Issue: 1 Pages: 76-84
- DOI
  10.1007/s12311-018-0955-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] Noncoding repeat expansions for ALS in Japan are associated with the ATXN8OS gene.2018
- Author(s)
  Hirano M, Samukawa M, Isono C, Saigoh K, Nakamura Y, Kusunoki S.
- Journal Title
  
  Neurol Genet
  
  Volume: 4 Issue: 4
- DOI
  10.1212/nxg.0000000000000252
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] The novel de novo mutation of KIF1A gene as the cause for Spastic paraplegia 30 in a Japanese case.2018
- Author(s)
  Yoshikawa K, Kuwahara M, Saigoh K, Ishiura H, Yamagishi Y, Hamano Y, Samukawa M, Suzuki H, Hirano M, Mitsui Y, Tsuji S, Kusunoki S.
- Journal Title
  
  eNeurologicalSci
  
  Volume: 2018 Pages: 34-37
- DOI
  10.1016/j.ensci.2018.11.026
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] Diagnosis of Parkinson's disease and the level of oxidized DJ-1 protein.2018
- Author(s)
  Yamagishi Y, Saigoh K, Saito Y, Ogawa I, Mitsui Y, Hamada Y, Samukawa M, Suzuki H, Kuwahara M, Hirano M, Noguchi N, Kusunoki S.
- Journal Title
  
  Neurosci Res.
  
  Volume: なし Pages: 58-62
- DOI
  10.1016/j.neures.2017.06.008
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09705, KAKENHI-PROJECT-17H03821
[Journal Article] Progression of Dysphagia in Spinocerebellar Ataxia Type 62017
- Author(s)
  Isono C, Hirano M, Sakamoto H, Ueno S, Kusunoki S, Nakamura Y.
- Journal Title
  
  Dysphagia
  
  Volume: 32 Issue: 3 Pages: 420-426
- DOI
  10.1007/s00455-016-9771-1
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] Time Course of Radiological Imaging and Variable Interindividual Symptoms in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Associated with p.Arg487His Mutation in the VCP Gene2017
- Author(s)
  Hirano Makito、Yamagishi Yuko、Yanagimoto Satoshi、Saigoh Kazumasa?、Nakamura Yusaku、Kusunoki Susumu
- Journal Title
  
  European Neurology
  
  Volume: 78 Issue: 1-2 Pages: 78-83
- DOI
  10.1159/000478906
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] Novel mutation in the SOD1 gene in a patient with early-onset, rapidly progressive amyotrophic lateral sclerosis2017
- Author(s)
  Okazaki Masahiro、Suzuki Hidekazu、Takahashi Yuji、Ishiura Hiroyuki、Goto Jun、Hirano Makito、Saigoh Kazumasa、Nakamura Yusaku、Naruse Hiroya、Mitsui Jun、Tsuji Shoji、Kusunoki Susumu
- Journal Title
  
  Neurology and Clinical Neuroscience
  
  Volume: 5 Issue: 6 Pages: 189-191
- DOI
  10.1111/ncn3.12153
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] Treatable Leukoencephalopathy in a Patient with Hypophosphatemia2016
- Author(s)
  Okazaki M, Hirano M, Iwatsu T, Yamana M, Suzuki H, Satou T, Kusunoki S.
- Journal Title
  
  Case Rep Neurol
  
  Volume: 8 Issue: 3 Pages: 264-271
- DOI
  10.1159/000454854
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] 日本のValosin-containing protein関連筋萎縮性側索硬化症2016
- Author(s)
  平野牧人、中村雄作、楠　進
- Journal Title
  
  臨床神経学
  
  Volume: 印刷中
- NAID
  130005149740
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] Valosin-containing protein-related amyotrophic lateral sclerosis in Japan2016
- Author(s)
  Hirano M, Nakamura Y, Kusunoki S
- Journal Title
  
  Rinsho Shinkeigaku
  
  Volume: 56 Issue: 4 Pages: 285-286
- DOI
  10.5692/clinicalneurol.cn-000845
- NAID
  130005149740
- ISSN
  0009-918X, 1882-0654
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] Histopathological features of a patient with Charcot-Marie-Tooth disease type 2U/AD-CMTax-MARS2016
- Author(s)
  Hirano M, Oka N, Hashiguchi A, Ueno S, Sakamoto H, Takashima H, Higuchi Y, Kusunoki S, Nakamura Y.
- Journal Title
  
  J Peripher Nerv Syst
  
  Volume: 301: Issue: 4 Pages: 61-64
- DOI
  10.1111/jns.12193
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09705
[Journal Article] Chondroitin sulfate β-1,4-N-acetylgalactosaminyltransferase-1 (ChGn-1) polymorphism; association with progression of multiple sclerosis.2016
- Author(s)
  Saigoh, K., Yoshimura, S., Izumikawa, T., Miyata, S., Tabara, Y., Matsushita, T., Miki, T., Miyamoto, K., Hirano, M., Kitagawa, H., Kita, J., and Kusunoki, S.
- Journal Title
  
  Neurosci. Res.
  
  Volume: 印刷中 Pages: 55-59
- DOI
  10.1016/j.neures.2016.01.002
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-23110003, KAKENHI-PUBLICLY-26110721, KAKENHI-PROJECT-15H04845, KAKENHI-PROJECT-25293014, KAKENHI-PROJECT-16K09705, KAKENHI-PROJECT-16H05088
[Journal Article] Differential Progression of Dysphagia in Heredity and Sporadic Ataxias Involving Multiple Systems2015
- Author(s)
  Isono C, Hirano M, Sakamoto H, Ueno S, Kusunoki S, Nakamura Y.
- Journal Title
  
  Eur Neurol
  
  Volume: 74 Issue: 5-6 Pages: 237-242
- DOI
  10.1159/000442252
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] VCP gene analyses in Japanese patients with sporadic amyotrophic lateral sclerosis identify a new mutation2015
- Author(s)
  Hirano M, Nakamura Y, Saigoh K, Sakamoto H, Ueno S, Isono C, Mitsui Y, Kusunoki S.
- Journal Title
  
  Neurobiol Aging
  
  Volume: 36 Issue: 3 Pages: 1604.e1-1604.e6
- DOI
  10.1016/j.neurobiolaging.2014.10.012
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25461297, KAKENHI-PUBLICLY-26110721
[Journal Article] Binding specificity of anti-HNK-1 IgM M-protein in anti-MAG neuropathy: Possible clinical relevance.2015
- Author(s)
  Hamada Y, Hirano M, Kuwahara M, Samukawa M, Takada K, Morise J, Yabuno K, Oka S, and Kusunoki S.
- Journal Title
  
  Neurosci Res.
  
  Volume: 91 Pages: 63-68
- DOI
  10.1016/j.neures.2014.09.010
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PLANNED-23110006, KAKENHI-PROJECT-24390225, KAKENHI-PROJECT-25461297, KAKENHI-PROJECT-26291021, KAKENHI-PUBLICLY-26110721
[Journal Article] Rotigotine Transdermal Patch Improves Swallowing in Dysphagic Patients with Parkinson's Disease.2015
- Author(s)
  Hirano M, Isono C, Sakamoto H, Ueno S, Kusunoki S, Nakamura Y.
- Journal Title
  
  Dysphagia
  
  Volume: 30 Issue: 4 Pages: 452-426
- DOI
  10.1007/s00455-015-9622-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene2015
- Author(s)
  1.Saigoh K, Mitsui J, Hirano, M, Sioyama M, Samukawa M, Ichikawa Y, Goto J, Tsuji S, Kusunoki S
- Journal Title
  
  Parkinsonism Relat Disord
  
  Volume: 21 Issue: 3 Pages: 332-334
- DOI
  10.1016/j.parkreldis.2014.12.028
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297, KAKENHI-PROJECT-25860700, KAKENHI-PUBLICLY-26110721
[Journal Article] The first nationwide survey and genetic analyses of Bardet-Biedl syndrome in Japan2015
- Author(s)
  Hirano M, Satake W, Ihara K, Tsug I, Kondo S, Saida K, Betsui H, Okubo K, Sakamoto H, Ueno S, Ikuno Y, Ishihara R, Iwahashi H, Ohishi M, Mano T, Yamashita T, Suzuki Y, Nakamura Y, Kusunoki S, Toda T
- Journal Title
  
  PLOS ONE
  
  Volume: 10 Issue: 9 Pages: e0136317-e0136317
- DOI
  10.1371/journal.pone.0136317
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591515, KAKENHI-PROJECT-26461613, KAKENHI-PROJECT-25461297, KAKENHI-PROJECT-25713015
[Journal Article] ALSとSQSTM12015
- Author(s)
  平野牧人
- Journal Title
  
  神経内科
  
  Volume: 82 Pages: 360-365
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene2014
- Author(s)
  Sakamoto H, Akamatsu M, Hirano M, Saigoh K, Ueno S, Isono C, Kusunoki S, Nakamura Y
- Journal Title
  
  Amyotroph Lateral Scler Frontotemporal Degener
  
  Volume: 未定
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene.2014
- Author(s)
  8.Sakamoto H, Akamatsu M, Hirano M, Saigoh K, Ueno S, Isono C, Kusunoki S, Nakamura Y.
- Journal Title
  
  Amyotroph Lateral Scler Frontotemporal Degener
  
  Volume: 15 Issue: 3-4 Pages: 312-314
- DOI
  10.3109/21678421.2013.873051
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] Overlapping demyelinating syndromes and anti-NMDA receptor encephalitis2014
- Author(s)
  Titulaer MJ, Hoeftberger R, Iizuka T, Leypoldt F, McCracken L, Cellucci T, Benson LA, Shu H, Irioka T, Hirano M, Singh G, Calvo AC, Kaida K, Morales PS, Wirtz PW, Yamamoto T, Reindl M, Rosenfeld MR, Graus F, Saiz A, Dalmau J.
- Journal Title
  
  Ann Neurol
  
  Volume: 未定 Issue: 3 Pages: 411-428
- DOI
  10.1002/ana.24117
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] Differences in dysphagia between spinocerebellar ataxia type 3 and type 62013
- Author(s)
  Isono C, Hirano M, Sakamoto H, Ueno S, Kusunoki S, Nakamura Y
- Journal Title
  
  Dysphagia
  
  Volume: 28 Issue: 3 Pages: 413-418
- DOI
  10.1007/s00455-013-9450-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] Ophthalmologic involvement in Japanese siblings with chorea-acanthocytosis caused by a novel chorein mutation.2013
- Author(s)
  Ogawa I, Saigoh K, Hirano M, Mtsui Y, Sugioka K, Takahashi J, Shimomura Y, Tani Y, Nakamura Y, Kusunoki S.
- Journal Title
  
  Parkinsonism Relat Disord
  
  Volume: 19 Issue: 10 Pages: 913-915
- DOI
  10.1016/j.parkreldis.2013.05.012
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] A case of severe ganciclovir-induced encephalopathy.2013
- Author(s)
  Sakamoto H, Hirano M, Nose K, Ueno S, Oki T, Sugimoto K, Nishioka T, Kusunoki S, Nakamura Y
- Journal Title
  
  Case Rep Neurol
  
  Volume: 5 Issue: 3 Pages: 183-186
- DOI
  10.1159/000355638
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461297
[Journal Article] Abnormal cystatin C levels in two patients with Bardet-Biedl syndrome2011
- Author(s)
  Hirano M, et al.
- Journal Title
  
  Clin Med Cas Rep Ins
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis2011
- Author(s)
  Hirano, M., Kokunai, Y., Nagai, A., Nakamura, Y., Saigoh, K., Kusunoki, S. and Takahashi, M. P
- Journal Title
  
  J. Neurol. Sci
  
  Volume: 309 Issue: 1-2 Pages: 9-11
- DOI
  10.1016/j.jns.2011.07.046
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097, KAKENHI-PROJECT-23591245
[Journal Article] Risks of inappropriate secretion of antidiuretic hormone in multiple system atrophy2011
- Author(s)
  Samukawa, M., Hirano, M., Sakamoto, H., Kitada, M., Kusunoki, S. and Nakamura, Y
- Journal Title
  
  Mov. Disord
  
  Volume: 26 Issue: 14 Pages: 2572-2573
- DOI
  10.1002/mds.23904
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onsetALS and ALS/dementia2011
- Author(s)
  Deng, H. X., Chen, W., Hong, S. T., Boycott, K. M., Gorrie, G. H., Siddique, N., Yang, Y., Fecto, F., Shi, Y., Zhai, H., Jiang, H., Hirano, M., Rampersaud, E., Jansen, G. H., Donkervoort, S., Bigio, E. H., Brooks, B. R., Ajroud, K., Sufit, R. L., Haines
- Journal Title
  
  Nature
  
  Volume: 477 Issue: 7363 Pages: 211-215
- DOI
  10.1038/nature10353
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] 遺伝性脊髄小脳変性症への言語聴覚療法-長期介入報告-2011
- Author(s)
  磯野千春, 中村雄作, 阪本光, 平野牧人, 山田郁子
- Journal Title
  
  言語聴覚研究
  
  Volume: 8 Pages: 63-65
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] Assembly defect due to a PSMB8 mutation reduces proteasome activity and causes the autoinflammatory disorder, Nakajo-Nishimura syndrome2011
- Author(s)
  Arima, K., Kinoshita, A., Mishima, H., Kanazawa, N., Kaneko, T., Mizushima, T., Ichinose, K., Nakamura, H., Tsujino, A., Kawakami, A., Matsunaka, M., Kasagi, S., Kawano, S., Kumagai, S., Ohmura, K., Mimori, T., Hirano, M., Ueno, S., Tanaka, K., Tanaka, M., Toyoshima, I., Sugino, H., Yamakawa, A., Tanaka, K., Niikawa, N., Furukawa, F., Murata, S., Eguchi, K., Ida, H., Yoshiura, K.
- Journal Title
  
  Proc.Natl.Acad.Sci.USA
  
  Volume: 108 Issue: 36 Pages: 14914-14919
- DOI
  10.1073/pnas.1106015108
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21000012, KAKENHI-PROJECT-21591097, KAKENHI-PROJECT-22591094, KAKENHI-PROJECT-22659071, KAKENHI-PROJECT-23500455, KAKENHI-PROJECT-23591651, KAKENHI-PROJECT-23657083, KAKENHI-PROJECT-23791115, KAKENHI-PROJECT-23791230
[Journal Article] The first nationwide survey of triple A syndrome in Japan2010
- Author(s)
  Hirano M, et al.
- Journal Title
  
  Ann Neurol
  
  Volume: 68
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] 認知症診療の未来を考える2010
- Author(s)
  花田一志、田中敬剛、平野牧人, 他3名
- Journal Title
  
  Japan Medicine Monthly
  
  Volume: 11 Pages: 6-9
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] Naturally-and experimentally-designed restorations of the Parkin gene deficit in autosomal recessive juvenile parkinsonism2010
- Author(s)
  Asai, H., Hirano, M., Kiriyama, T., Ikeda, M. and Ueno, S
- Journal Title
  
  Biochem. Biophys. Res. Commun
  
  Volume: 391 Issue: 1 Pages: 800-805
- DOI
  10.1016/j.bbrc.2009.11.141
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] Cerebrospinal fluid-orexin levels and sleep attacks in four patients with Parkinson's disease2009
- Author(s)
  Asai, H., Hirano, M., Furiya, Y., Udaka, F., Morikawa, M., Kanbayashi, T., Shimizu, T. and Ueno, S
- Journal Title
  
  Clin. Neurol. Neurosurg
  
  Volume: 111 Issue: 4 Pages: 341-344
- DOI
  10.1016/j.clineuro.2008.11.007
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] 総説神経疾患と塩基除去修復2009
- Author(s)
  平野牧人, 森俊雄, 上野聡
- Journal Title
  
  放射線生物研究 44
  
  Pages: 285-293
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin.2009
- Author(s)
  Asai H, Hirano M, Shimada K, Kiriyama T, Furiya Y, Ikeda M, Iwamoto T, Mori T, Nishinaka K, Konishi N, Udaka F, Ueno S
- Journal Title
  
  Hum Mol Genet,Epub 1;18(19)
  
  Pages: 3533-3543
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin2009
- Author(s)
  Asai, H., Hirano, M., Shimada, K., Kiriyama, T., Furiya, Y., Ikeda, M., Iwamoto, T., Mori, T., Nishinaka, K., Konishi, N., Udaka, F. and Ueno, S
- Journal Title
  
  Hum. Mol. Genet
  
  Volume: 18 Issue: 19 Pages: 3533-3543
- DOI
  10.1093/hmg/ddp298
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591097
[Journal Article] Naturally-and experimentally-designed restorations of the Parkin gene deficit in autosomal recessive juvenile parkinsonism.2009
- Author(s)
  Asai H, Hirano M, Kiriyama T, Ikeda M, Ueno S
- Journal Title
  
  Biochem Biophys Res Commun,Epub 1;391(1),Nov 27
  
  Pages: 800-805
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] Cerebrospinal fluid-orexin levels and sleep attacks in four patients with Parkinson's disease2009
- Author(s)
  Asai H, Hirano M, Furiya Y, Udaka F, Morikawa M, Kanbayashi T, Shimizu T, Ueno S.
- Journal Title
  
  Clin Neurol Neurosurg 111
  
  Pages: 341-344
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Treatable fluctuating mental impairment in a patient with Bardet-Biedl syndrome2009
- Author(s)
  Tonomura Y, Hirano M, Shimada K, Asai H, Ikeda M, Kataoka H, Tanaka I, Konishi N, Ueno S.
- Journal Title
  
  Clin Neurol Neurosurg 111
  
  Pages: 102-104
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] 総説神経疾患と塩基除去修復2009
- Author(s)
  平野牧人、森俊雄、上野聡
- Journal Title
  
  放射線生物研究 44巻
  
  Pages: 285-293
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] 総説神経疾患と塩基除去修復2009
- Author(s)
  平野牧人, 森俊雄, 上野聡
- Journal Title
  
  放射線生物研究 44
  
  Pages: 285-293
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] Complete recovery of an aged patient with Guillain-Barre syndrome associated with multiple IgM anti-ganglioside antibodies2008
- Author(s)
  Furiya Y, Hirano M, Kusunoki S, Ueda M, Sugie K, Nishiwaki T, Ueno S.
- Journal Title
  
  Muscle Nerve 38
  
  Pages: 1630-1633
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Identification of a nuclear localization signal of XRCC1 overcoming impaired nuclear import in triple A syndrome.2008
- Author(s)
  Kiriyama T, Hirano M, Asai H, Furiya Y, Kanbayashi T, Ikeda M, Ueno S
- Journal Title
  
  Ann Neurol 64
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] Cerebrospinal fluid-orexin levels and sleep attacks in four patients with Parkinson's disease.2008
- Author(s)
  Asai H, Hirano M, Furiya Y, Udaka F, Morikawa M, Kanbayashi T, Shimizu T, Ueno S
- Journal Title
  
  Clin Neurol Neurosurg 111(4)
  
  Pages: 341-344
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] Fixed epiglottis associated with subthalamic nucleus stimulation in Parkinson's disease2008
- Author(s)
  Yanase M, Kataoka H, Kawahara M, Hirabayashi H, Yamanaka T, Hirano M, Ueno S.
- Journal Title
  
  J Neurol Neurosurg Psychiatry 79
  
  Pages: 332-333
- NAID
  10024369564
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients2008
- Author(s)
  Nishiwaki T, Kobayashi N, Iwamoto T, Yamamoto A, Sugiura S, Liu YC, Sarasin A, Okahashi Y, Hirano M, Ueno S, Mori T.
- Journal Title
  
  DNA Repair (Amst) 7
  
  Pages: 1990-1998
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach2008
- Author(s)
  Deng H-X, Jiang H, Fu R, Zhai H, Shi Y, Liu E, Hirano M, C. Dal Canto M, Siddique T.
- Journal Title
  
  Hum Mol Genet 17
  
  Pages: 2310-2319
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Restoration of nuclear-import failure caused by triple A syndrome and oxidative stress.2008
- Author(s)
  Kiriyama T, Hirano M, Asai H, Ikeda M, Furiya Y, Ueno S
- Journal Title
  
  Biochem Biolphys Res Commnun 374
  
  Pages: 631-634
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] Restoration of nuclear-import failure caused by triple A syndrome and oxidative stress2008
- Author(s)
  Kiriyame T, Hirano M, Asai H, Ikeda M, Furiya Y, Ueno S.
- Journal Title
  
  Biochem Biophys Res Commun 374
  
  Pages: 631-634
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients.2008
- Author(s)
  Nishiwaki T, Kobayashi N, Iwamoto T, Yamamoto A, Sugiura S, Liu YC, Sarasin A, Okahashi Y, Hirano M, Ueno S, Mori T
- Journal Title
  
  DNA repair 7
  
  Pages: 1990-1998
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach.2008
- Author(s)
  Deng HX, Jiang H, Fu R, Zhai H, Shi Y, Liu E, Hirano M, Dal Canto MC, Siddique T.
- Journal Title
  
  Hum Mol Genet,Epub,Erratum in: Hum Mol Genet. 17(15),1;18(3)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] Treatable fluctuating Parkinsonism and dementia in a patient with a dural arteriovenous fistula2007
- Author(s)
  Kajitani M, Yagura H, Kawahara M, Hirano M, Ueno S, Fujimoto K, Sakaki T, Taoka T, Nakagawa H, Kichikawa K.
- Journal Title
  
  Mov Disord 22
  
  Pages: 437-439
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Sympathetic disturbances increase risk of sudden cardiac arrest in sporadic ALS2007
- Author(s)
  Asai H, Hirano M, Udaka F, Shimada K, Oda M, Kubori T, Nishinaka K, Tsujimura T, Izumi Y, Konishi N, Matsumoto S, Kameyama M, Ueno S.
- Journal Title
  
  J Neurol Sci 254
  
  Pages: 78-83
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Short half-lives of ataxia-associated aprataxin proteins in neuronal cells2007
- Author(s)
  Hirano M, Asai H, Kiriyama T, Furiya Y, Iwamoto T, Nishiwaki T, Yamamoto A, Mori T, Ueno S.
- Journal Title
  
  Neurosci Lett 419
  
  Pages: 184-187
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Diffusivity and diffusion anisotropy of cerebellar peduncles in cases of spinocerebe llar degenerative disease2007
- Author(s)
  Taoka T, Kin T, Nakagawa H, Hirano M, Sakamoto M, Wada T, Takayama K, Wuttikul C, Iwasaki S, Ueno S, Kichikawa K.
- Journal Title
  
  Neuroimage 37
  
  Pages: 387-393
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Mutant ALADIN impairs selective nuclear import and DNA repair in triple Asyndrome2007
- Author(s)
  Hirano M, et. al.
- Journal Title
  
  Ann Neurol 62
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Peripheral neuropathy in chromosome16q22.1-linked autosomal dominant cerebellar ataxia2007
- Author(s)
  Furiya Y, Hirano M, Nomura M, Asai H, Kiriyama T, Ueno S.
- Journal Title
  
  J Neurol Neurosurg Psychiatry 78
  
  Pages: 1009-1011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Short half-lives of ataxia-associated aprataxin proteins in neuronal cells2007
- Author(s)
  Hirano M, et. al.
- Journal Title
  
  Neurosci Lett 419
  
  Pages: 184-187
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] SPECT revealed cortical dysfunction in a patient who had genetically definite megalencephalic leukoencephalopathy with subcortical cysts2007
- Author(s)
  Kiriyama T, Tanizawa E, Hirano M, Shinkai T, Asai H, Furiya Y, Ueno S.
- Journal Title
  
  Clin Neurol Neurosurg 109
  
  Pages: 526-530
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] Genetics of spinocerebellar ataxias2004
- Author(s)
  Makito Hirano
- Journal Title
  
  J.Nara Med Assoc. 55・2
  
  Pages: 73-80
- NAID
  120004972856
- Data Source
  KAKENHI-PROJECT-15790453
[Journal Article] Loss of function mechanism in aprataxin-related early-onset ataxia2004
- Author(s)
  Makito Hirano
- Journal Title
  
  Biochem.Biophys.Res.Commun. 322・2
  
  Pages: 380-386
- Data Source
  KAKENHI-PROJECT-15790453
[Journal Article] Novel splice variants increase molecular diversity of aprataxin, the gene responsible for early-onset ataxia with ocular motor apraxia and hypoalbuminemia2004
- Author(s)
  Makito Hirano
- Journal Title
  
  Neurosci.Lett. 366・2
  
  Pages: 120-125
- Data Source
  KAKENHI-PROJECT-15790453
[Journal Article] Alternative splicing may contribute to tissue specific phenotype in aprataxin-related ataxia2004
- Author(s)
  Makito Hirano
- Journal Title
  
  Ann.Neurol. 56・suppl 8
- Data Source
  KAKENHI-PROJECT-15790453
[Journal Article] 総説神経疾患と塩基除去修復
- Author(s)
  平野牧人, 他2名
- Journal Title
  
  放射線生物研究 (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Journal Article] 総説神経疾患と塩基除去修復
- Author(s)
  平野牧人, 森俊雄, 上野聡
- Journal Title
  
  放射線生物研究 (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591008
[Journal Article] 総説神経疾患と塩基除去修復
- Author(s)
  平野牧人, 森俊雄, 上野聡
- Journal Title
  
  放射線生物研究 (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] RFC1 repeat expansions in neuroimmunological and neurodegenerative diseases2024
- Author(s)
  Makito Hirano, Yuko Yamagishi, Motoi Kuwahara, Makoto Samukawa, Kanako Fujii, Nobuyuki Oka, Misako Kaido, Toshihide Takeuchi, Kazumasa Saigoh, Yusaku Nakamura, Susumu Kusunoki, Hiroshi Takashima, Yoshitaka Nagai
- Organizer
  第65回　日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-22K07510
[Presentation] Phenotypic variation and therapeutic strategy of SCA8-associated amyotrophic lateral sclerosis2022
- Author(s)
  Makito Hirano, Toshiyuki Takehara, Shigeo Murayama, Yuishin Izumi, Makoto Samukawa, Tomoyasu Matsubara, Yuko Saito, Kazumasa Saigoh, Yusaku Nakamura, Kanji Fukuda, Susumu Kusunoki, Yoshitaka Nagai
- Organizer
  第63回　日本神経学会総会
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] Phenotypic variation and therapeutic strategy of SCA8-associated amyotrophic lateral sclerosis2022
- Author(s)
  Makito Hirano, Toshiyuki Takehara, Shigeo Murayama, Yuishin Izumi, Makoto Samukawa, Tomoyasu Matsubara, Yuko Saito, Kazumasa Saigoh, Yusaku Nakamura, Kanji Fukuda Susumu Kusunoki, Yoshitaka Nagai
- Organizer
  第63回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-22K07510
[Presentation] Gene analyses for spinocerebellar ataxia type 2 identify neuropathy phenotype in Japan.2022
- Author(s)
  Rino Inada, Makito Hirano, Nobuyuki Oka, Makoto Samukawa, Kazumasa Saigoh, Hidekazu Suzuki, Fukashi Udaka, Akihiro Hashiguchi, Hiroshi Takashima, Yukihiro Hamada, Yusaku Nakamura, Yoshitaka Nagai ,Susumu Kusunoki
- Organizer
  第63回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-22K07510
[Presentation] Gene analyses for spinocerebellar ataxia type 2 identify neuropathy phenotype in Japan.2022
- Author(s)
  Rino Inada, Makito Hirano, Nobuyuki Oka, Makoto Samukawa, Kazumasa Saigoh, Hidekazu Suzuki, Fukashi Udaka, Akihiro Hashiguchi, Hiroshi Takashima, Yukihiro Hamada, Yusaku Nakamura, Susumu Kusunoki
- Organizer
  第63回　日本神経学会総会
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] 脊髄小脳失調症8型遺伝子異常を有する筋萎縮性側索硬化症患者の嚥下機能2021
- Author(s)
  磯野千春、平野牧人、福田寛二、寒川　真、西郷和真、中村雄作、楠　進
- Organizer
  第62回　日本神経学会総会
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] パーキンソン病と関連疾患における新しい分子病態と嚥下障害～治療と対策～2021
- Author(s)
  平野牧人
- Organizer
  第62回　日本神経学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] 神経筋疾患の嚥下障害　　　　　～基本から最新知見まで～2021
- Author(s)
  平野牧人
- Organizer
  第61回日本神経学会
- Invited
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] The first patient with pathologically-definite ATXN8OS-associated amyotrophic lateral sclerosis2020
- Author(s)
  Makito Hirano, Shigeo Murayama, Yuishin Izumi, Makoto Samukawa, Tomoyasu Matsubara, Kazumasa Saigoh, Yusaku Nakamura, Susumu Kusunoki
- Organizer
  第61回日本神経学会
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] Non-coding repeats in the ATXN8OS gene are expanded in Japanese patients with amyotrophic lateral sclerosis2019
- Author(s)
  Makito Hirano, Makoto Samukawa, Chiharu Isono, Kazumasa Saigoh, Yusaku Nakamura, Susumu Kusunoki
- Organizer
  2019 Annual Meeting - American Academy of Neurology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] NON-CODING REPEAT EXPANSIONS IN THE ATXN8OS GENE ARE IDENTIFIED IN JAPANESE PATIENTS WITH AMYOTROPHIC LATERAL SCLEROSIS.2019
- Author(s)
  Makito Hirano, Makoto Samukawa, Chiharu Isono, Kazumasa Saigoh, Yusaku Nakamura, Susumu Kusunoki
- Organizer
  World Congress of Neurology 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] Clinical features and progression of dysphagia in bulbar-onset or limb-onset amyotrophic lateral sclerosis between patients with genetic mutations and those without mutations2019
- Author(s)
  Chiharu Isono, Makito Hirano, Kanji Fukuda, Makoto Samukawa, Kazumasa Saigoh, Yusaku Nakamura, Susumu Kusunoki
- Organizer
  World Congress of Neurology 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K07984
[Presentation] Analyses of non-coding repeat expansions in Japanese patients with amyotrophic lateral sclerosis reveals mutations in the ATXN8OS gene.2018
- Author(s)
  Makito Hirano, Makoto Samukawa, Chiharu Isono, Kazumasa Saigoh,, Yusaku Nakamura, Susumu Kusunoki
- Organizer
  American Neurological Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] Characteristics and progression of dysphagia in amyotrophic lateral sclerosis associated with genetic mutations.2018
- Author(s)
  Chiharu Isono, Makito Hirano, Kanji Fukuda, Susumu Kusunoki, Yusaku Nakamura
- Organizer
  American Neurological Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] Significant relationship of CTA/CTG repeat sizes with age at onset and phenotype in SCA82018
- Author(s)
  Makoto Samukawa, Makito Hirano, Kazumasa Saigoh, Shigeru Kawai, Yukihiro Hamada, Daisuke Takahashi, Yusaku Nakamura, Susumu Kusunoki
- Organizer
  American Neurological Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] p62変異型筋萎縮性側索硬化症iPS細胞を用いた疾患機序解明の試み2018
- Author(s)
  竹原俊幸,平野牧人,寺村岳士,小野寺勇太,楠進,江良拓実,福田寛二
- Organizer
  再生医療学会
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] Mutations in the COQ2 gene in atypical phenotypes of neurodegenerative diseases and supplementation of coenzyme Q102017
- Author(s)
  Makito Hirano, Yusaku Nakamura, Kazumasa Saigoh, Makoto Samukawa, Susumu Kusunoki
- Organizer
  American Neurological Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] Comparison of clinical features between a patient with intermediate CTA/CTG repeats and patients with 80 of longer CTA/CTG repeats in Spinocerebellar ataxia type 82017
- Author(s)
  Makoto Samukawa, Makito Hirano, Kazumasa Saigoh, Susumu Kusunoki
- Organizer
  American Neurological Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] Genetic analyses and counselling of sporadic amyotrophic lateral sclerosis in Japan2016
- Author(s)
  Makito Hirano, Yusaku Nakamura, Kazumasa Saigoh, Hikaru Sakamoto, Shuichi Ueno, Hidekazu Suzuki, Susumu Kusunoki
- Organizer
  Annual Meeting of American Neurological Association
- Place of Presentation
  ボルチモアマリオットホテル（米国ボルチモア）
- Year and Date
  2016-10-16
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] パーキンソン病とMSAの摂食嚥下障害2016
- Author(s)
  平野牧人
- Organizer
  日本神経学会総会
- Place of Presentation
  神戸国際会議場（神戸）
- Year and Date
  2016-05-18
- Invited
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] Progression of dysphagia in spinocerebellar ataxia type 62016
- Author(s)
  Chiharu Isono, Makito Hirano, Hikaru Sakamoto, Shuichi Ueno, Susumu Kusunoki, Yusaku Nakamura
- Organizer
  Annual Meeting of American Neurological Association
- Place of Presentation
  ボルチモアマリオットホテル（米国ボルチモア）
- Year and Date
  2016-10-16
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] Comparison of improvement in swallowing functions between patients with Parkinson’s disease treated with rotigotine and those with levodopa2016
- Author(s)
  Makito Hirano, Chiharu Isono, Hikaru Sakamoto, Shuichi Ueno, Susumu Kusunoki, Yusaku Nakamura
- Organizer
  Annual Meeting of American Neurological Association
- Place of Presentation
  ボルチモアマリオットホテル（米国ボルチモア）
- Year and Date
  2016-10-16
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] Novel mutations and genetic counseling in sporadic amyotrophic lateral sclerosis2016
- Author(s)
  Makito Hirano, Yusaku Nakamura, Kazumasa Saigoh, Hikaru Sakamoto, Shuichi Ueno, Hidekazu Suzuki, Susumu Kusunoki
- Organizer
  日本神経学会総会
- Place of Presentation
  神戸国際会議場（神戸）
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-16K09705
[Presentation] 孤発性筋萎縮性側索硬化症の遺伝子解析による新規変異同定とカウンセリングの問題点2015
- Author(s)
  平野牧人、中村雄作、西郷和真、阪本　光、上野周一、鈴木秀和、楠　進
- Organizer
  人類遺伝学会
- Place of Presentation
  京王プラザホテル (東京)
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] Analyses of the VCP gene in Japanese patients with sporadic amyotrophic lateral sclerosis identify the novel mutation that increases susceptibility to oxidative stress2015
- Author(s)
  Makito Hirano, MD, PhD1, 2, Yusaku Nakamura, Kazumasa Saigoh, Hikaru Sakamoto, Shuichi Ueno, Chiharu Isono, Susumu Kusunoki
- Organizer
  The Annual Meeting of American Neurological Association
- Place of Presentation
  Chicago (米国)
- Year and Date
  2015-09-27
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] Analysis of sporadic amyotrophic lateral sclerosis detects a novel VCP mutation2015
- Author(s)
  Makito Hirano, Yusaku Nakamura, Kazumasa Saigoh, Hikaru Sakamoto, Shuichi Ueno, MD, Susumu Kusunoki
- Organizer
  神経学会総会
- Place of Presentation
  朱鷺メッセ　(新潟市)
- Year and Date
  2015-05-20
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] Improvement of swallowing functions by rotigotine transdermal patch in patients with Parkinson’s disease2015
- Author(s)
  Chiharu Isono, Makito Hirano, Hikaru Sakamoto, Shuichi Ueno, Susumu Kusunoki, Yusaku Nakamura
- Organizer
  The Annual Meeting of American Neurological Association
- Place of Presentation
  Chicago (米国)
- Year and Date
  2015-09-27
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] p62/SQSTM1/遺伝子変異を有する筋萎縮性側索硬化症の線維芽細胞とiPS細胞の解析2013
- Author(s)
  平野牧人、中村雄作、寺村岳士、　江良択実、西郷和真、阪本　光、上野周一、福田寛二、楠　進
- Organizer
  日本人類遺伝学会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] 孤発性筋萎縮性側索硬化症におけるC9ORF72, UBQLN2, PFN1, p62/SQSTM1遺伝子解析2013
- Author(s)
  平野牧人、中村雄作、阪本　光、上野周一、西郷和真、楠　進
- Organizer
  日本神経学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] Novel mutations in the SQSTM1 gene encoding p62 in Japanese patients with sporadic amyotrophic lateral sclerosis2013
- Author(s)
  Makito Hirano, Yusaku Nakamura, Kazumasa Saigoh, Hikaru Sakamoto, Shuichi Ueno, Chiharu Isono, Susumu Kusunoki
- Organizer
  The Annual Meeting of American Neurological Association
- Place of Presentation
  ニューオリンズ
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] 孤発性筋萎縮性側索硬化症におけるp62/SQSTM1遺伝子の解析2013
- Author(s)
  平野牧人、中村雄作、阪本　光、上野周一、西郷和真、楠　進
- Organizer
  Neuro2013
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] SCA3およびSCA6における嚥下障害の経過と特徴2011
- Author(s)
  平野牧人, 他
- Organizer
  第29回日本神経治療学会
- Place of Presentation
  福井
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Oxidative stress-induced DNA damage in neurodegenerative diseases-autosomal dominant and recessive ataxia and motor neuron diseases-2011
- Author(s)
  Hirano, M., 他
- Organizer
  1^<st> RIRBM International Symposium Genome damage and non-cancerous diseases
- Place of Presentation
  Hiroshima
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] The first nationwide survey of Bardet-Biedl syndrome in Japan2011
- Author(s)
  Hirano, M., 他
- Organizer
  136th Annual meeting of American Neurological Association
- Place of Presentation
  San Diego, USA
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] UBQLN2は筋萎縮性側索硬化症の新規原因遺伝子である2011
- Author(s)
  平野牧人, ら
- Organizer
  第56回日本人類遺伝学会
- Place of Presentation
  幕張メッセ(千葉市)
- Year and Date
  2011-11-12
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Oxidative stress-induced DNA damage in neurodegenerative diseases-autosomal dominant and recessive ataxia and motor neuron diseases-2011
- Author(s)
  Hirano M, 他3名
- Organizer
  1^<st> RIRBM International Symposium Genome damage and non-cancerous diseases
- Place of Presentation
  広島
- Year and Date
  2011-03-03
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] バルデー・ビードル症候群の全国実態調査2011
- Author(s)
  平野牧人, ら
- Organizer
  第52回日本神経学会
- Place of Presentation
  名古屋国際会議場(名古屋市)
- Year and Date
  2011-05-20
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] UBQLN2は筋萎縮性側索硬化症の新規原因遺伝子である2011
- Author(s)
  平野牧人, 他
- Organizer
  第56回日本人類遺伝学会
- Place of Presentation
  大宮
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 多系統萎縮症と抗利尿ホルモン不適合分泌症候群の関連2011
- Author(s)
  平野牧人, 他
- Organizer
  第52回日本神経学会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] バルデー・ビードル症候群の全国実態調査2011
- Author(s)
  平野牧人, 他
- Organizer
  第35回日本遺伝カウンセリング学会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 本邦におけるバルデー・ビードル症候群の実態2011
- Author(s)
  平野牧人, 他
- Organizer
  第52回日本神経学会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] The first nationwide survey of Bardet-Biedl syndrome in Japan2011
- Author(s)
  Hirano M, et al
- Organizer
  136th Annual meeting of American Neurological Association
- Place of Presentation
  Manchester Grand Hyatt (San Diego, USA)
- Year and Date
  2011-09-26
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] The first nationwide survey of triple A syndrome in Japan2010
- Author(s)
  Hirano, M., 他
- Organizer
  135th Annual meeting of American Neurological Association
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Japanese patients with Bardet-Biedl syndrome2010
- Author(s)
  Hirano, M., 他
- Organizer
  Neuro2010(日本神経化学会総会)
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Spontaneous and Experimental Exon Skipping Restores the Parkin Gene Deficits in Autosomal Recessive Juvenile Parkinsonism2010
- Author(s)
  Hirano, M., 他
- Organizer
  135th Annual meeting of American Neurological Association
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 常染色体劣性パーキンソニズムのparkin機能欠損に対するアンチセンス治療の検討2010
- Author(s)
  平野牧人, 他
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Alzheimer患者における内臓脂肪面積とadipocytokinesの検討2010
- Author(s)
  平野牧人, 他
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Phenotype-Genotype Relationship of Triple A Syndrome2010
- Author(s)
  Hirano, M., 他
- Organizer
  135th Annual meeting of American Neurological Association
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 運動ニューロン病様AAA症候群の全国実態調査および臨床遺伝学的研究連2010
- Author(s)
  平野牧人, 他
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] FUS関連筋萎縮側索硬化症細胞の酸化ストレスに対する脆弱性とDNA損傷の蓄積2010
- Author(s)
  平野牧人, 他
- Organizer
  第53回放射線影響学会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 多系統萎縮症における抗利尿ホルモン不適合分泌症候群の合併2010
- Author(s)
  平野牧人, 他
- Organizer
  第63回日本自律神経学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] パーキン関連パーキンソニズムにおけるエクソンスキッピング誘導療法2010
- Author(s)
  平野牧人, 他
- Organizer
  第28回日本神経治療学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] The influence of antihypertensive drugs, rennin-angiotensin blockades, on cognitive decline and insulin resistance in Alzheimer's disease2010
- Author(s)
  Hirano, M., 他
- Organizer
  135th Annual meeting of American Neurological Association
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 常染色体劣性遺伝パーキンソンニズムのparkin機能欠損に対するアンチセンス治療の検討2010
- Author(s)
  浅井宏英、平野牧人、桐山敬生、池田真徳、上野聡
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2010-05-20
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] Spontaneous and Experimental Exon Skipping Restores the Parkin Gene Deficits in Autosomal Recessive Juvenile Parkinsonism.2010
- Author(s)
  Asai H, Hirano M, Kiriyama T, Ikeda M, Horikawa H, Ueno S
- Organizer
  135^<th> Annual Meeting of the American Neurological Association
- Place of Presentation
  San Francisco, U.S.A
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] 本邦におけるバルデー・ビードル症候群2010
- Author(s)
  平野牧人, 他
- Organizer
  人類遺伝学会第55回大会
- Place of Presentation
  大宮
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] PMP22遺伝子欠失を伴う遺伝性圧脆弱性ニューパチーにおける神経根のMRI所見2009
- Author(s)
  平野牧人, 他
- Organizer
  第50回日本神経学会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Kinase activities of muta nt protein kinase C gamma, a protein cau sative for spinocerebellar ataxia type 14, and neuronal cell death under oxidative st ress2009
- Author(s)
  Hirano, M., 他
- Organizer
  134th Annual meeting of American Neurological Association
- Place of Presentation
  Baltimore, USA
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] DNA修復蛋白XRCC1の核局在シグナルを用いたAprataxinとSOD1の核内輸送2009
- Author(s)
  平野牧人, 他
- Organizer
  第50回日本神経学会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 遺伝性脊髄小脳変性症14型の原因となる変異protein kinase Cγ活性と蛋白凝集の関連2009
- Author(s)
  平野牧人, 浅井宏英, 桐山敬生, 池田真徳, 降矢芳子, 上野聡
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] DNA単鎖切断修復蛋白アプラタキシンと神経疾患～常染色体優性・劣性小脳失調症とAAA症候群～2009
- Author(s)
  平野牧人, 他6名
- Organizer
  第52回放射線影響学会
- Place of Presentation
  広島
- Year and Date
  2009-11-11
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] 遺伝性脊髄小脳変性症14型の原因となる変異protein kinase Cg活性と蛋白凝集の関連2009
- Author(s)
  平野牧人, 他
- Organizer
  第50回日本神経学会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Kinase activities of mutant protein kinase C gamma, a protein causative for spinocerebellar ataxia type 14, and neuronal cell death under oxidative stress.2009
- Author(s)
  浅井宏英, 平野牧人, 池田真徳, 上野聡
- Organizer
  The 134th Annual Meeting of American Neurological Association
- Place of Presentation
  Baltimore
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] Aggregate formation and activities of mutant protein kinase C gamma, a protein causative for spinocerebellar ataxia type 142009
- Author(s)
  Hirano, M., 他
- Organizer
  134th Annual meeting of American Neurological Association
- Place of Presentation
  Baltimore, USA
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 酸化ストレス下における遺伝性脊髄小脳変性症14型の原因となる変異protein kinase Cγ活性と細胞死の関連2009
- Author(s)
  平野牧人, 他
- Organizer
  第50回日本神経学会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] DNA単鎖切断修復蛋白アプラタキシンと神経疾患.常染色体優性・劣性小脳失調症とAAA症候群2009
- Author(s)
  平野牧人、森俊雄、池田真徳、浅井宏英、桐山敬生、降矢芳子、上野聡
- Organizer
  第52回日本放射線影響学会大会
- Place of Presentation
  広島
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] MRI abnormalities of cervical roots in hereditary neuropahty with liability to pressure palsies2009
- Author(s)
  Hirano, M., 他
- Organizer
  134th Annual meeting of American Neurological Association
- Place of Presentation
  Baltimore, USA
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Japanese patients with triple A syndrome2009
- Author(s)
  Hirano, M., 他
- Organizer
  6th Congress of International Society for Autonimic Neuroscience
- Place of Presentation
  Sydney, Australia
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 遺伝性脊髄小脳変性症14型の原因となる変異 protein kinase Cγ活性と蛋白凝集の関連2009
- Author(s)
  平野牧人, 他5名
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-21
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Aggregate formation and activities of mutant protein kinase C gamma, a protein causative for spinocerebellar ataxia type 142009
- Author(s)
  平野牧人, 他5名
- Organizer
  135^<th> Annual meeting of American Neurological Association
- Place of Presentation
  Baltimore, USA
- Year and Date
  2009-10-13
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] DNA修復蛋白XRCC1の核局在シグナルを用いたAprataxinとSOD1の核内輸送2009
- Author(s)
  桐山敬生、平野牧人、浅井宏英、池田真徳、降矢芳子、上野聡
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] Aggregate formation and activities of mutant protein kinase C gamma, a protein causative for spinocerebellar ataxia type 14.2009
- Author(s)
  平野牧人, 浅井宏英, 桐山敬生, 池田真徳, 降矢芳子, 上野聡
- Organizer
  The 134th Annual Meeting of American Neurological Association
- Place of Presentation
  Baltimore
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] Alzheimer患者におけるメタボリックシンドロームと内臓脂肪面積の検討2009
- Author(s)
  平野牧人, 他
- Organizer
  第50回日本神経学会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] DNA単鎖切断修復蛋白アプラタキシンと神経疾患～常染色体優性・劣性小脳失調症とAAA症候群～2009
- Author(s)
  平野牧人, 他6名
- Organizer
  第52回放射線影響学会
- Place of Presentation
  広島
- Year and Date
  2009-11-11
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] 酸化ストレス下における遺伝性脊髄小脳変性症14型の原因となる変異protein kinase Cγ活性と細胞死の関連2009
- Author(s)
  浅井宏英、平野牧人、桐山敬生、池田真徳、降矢芳子、上野聡
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] DNA単鎖切断修復蛋白アプラタキシンと神経疾患～常染色体優性・劣性小脳失調症とAAA症候群～2009
- Author(s)
  平野牧人, 他
- Organizer
  日本放射線影響学会
- Place of Presentation
  広島
- Data Source
  KAKENHI-PROJECT-21591097
[Presentation] Aggregate formation and activities of mutant protein kinase C gamma, a protein causative for spinocerebellar ataxia type 142009
- Author(s)
  平野牧人, 他5名
- Organizer
  135^<th> Annual meeting of American Neurological Association
- Place of Presentation
  Baltimore, USA
- Year and Date
  2009-10-13
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] 遺伝性脊髄小脳変性症14型の原因となる変異 protein kinase Cγ活性と蛋白凝集の関連2009
- Author(s)
  平野牧人, 他5名
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-21
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] In vivo DNA damage accumulation in aprataxin-related ataxia.2008
- Author(s)
  Hirano M, 他9名
- Organizer
  134^<th> Annual meeting of American Neurological Association
- Place of Presentation
  Salt Lake City, USA
- Year and Date
  2008-09-23
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] 酸化的DNA損傷修復系への小脳失調原因蛋白アプラタキシンの機能的関与2008
- Author(s)
  平野牧人, 他7名
- Organizer
  第48回放射線影響学会
- Place of Presentation
  小倉
- Year and Date
  2008-11-20
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] In Vivo DNA Damage Accumulation in Aprataxin-Related Ataxia.2008
- Author(s)
  Hirano M, Asai H, Aoki M, shimada K, Fuiya Y, Kiriyama T, Ikeda M, Konishi N, Itoyama Y, Ueno S
- Organizer
  133rd Annual Meeting of the American Neurological Association
- Place of Presentation
  Salt Lake City, UT
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] 酸化的DNA損傷修復系への小脳失調原因蛋白アプラタキシンの機能的関与2008
- Author(s)
  平野牧人、浅井宏英、桐山敬生、池田真徳、降矢芳子、森俊雄、安井明、上野聡
- Organizer
  第51回日本放射線影響学会
- Place of Presentation
  小倉
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] 眼球運動失行と低アルブミン血症を伴う早発型脊髄小脳失調症におけるDNA損傷の蓄積2008
- Author(s)
  平野牧人, 他8名
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  横浜
- Year and Date
  2008-05-16
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] 酸化的DNA損傷修復系への小脳失調原因蛋白アプラタキシンの機能的関与2008
- Author(s)
  平野牧人, 他7名
- Organizer
  第48回放射線影響学会
- Place of Presentation
  小倉
- Year and Date
  2008-11-20
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] 眼球運動失行と低アルブミン血症を伴う早発型脊髄小脳失調症におけるDNA損傷の蓄積2008
- Author(s)
  平野牧人, 上野聡, 他7名
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  横浜
- Year and Date
  2008-05-16
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] In vivo DNA damage accumulation in aprataxin-related ataxia2008
- Author(s)
  Hirano M, 他9名
- Organizer
  134^<th> Annual meeting of American Neurological Association
- Place of Presentation
  Salt Lake City, USA
- Year and Date
  2008-09-23
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] In vivo DNA damage accumulation in aprataxin-related ataxia.2008
- Author(s)
  Hirano M, 他9名
- Organizer
  134^<th> Annual meeting of American Neurological Association
- Place of Presentation
  Salt Lake City, USA
- Year and Date
  2008-09-23
- Data Source
  KAKENHI-PROJECT-20591008
[Presentation] ALADINI482S causes hypersensitivity to oxidative stress by selective failure of DNA repair protein import in triple A syndrome2007
- Author(s)
  5. Asai H, Hirano M, 他5名
- Organizer
  Neuroscience
- Place of Presentation
  San Diego, USA
- Year and Date
  2007-11-05
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] 新たなALADIN遺伝子変異を伴うTriple A症候群における、小脳失調原因蛋白aprataxinの核内輸送障害2007
- Author(s)
  浅井宏英、平野牧人, 他3名
- Organizer
  第48回日本神経学会総会
- Place of Presentation
  名古屋
- Year and Date
  2007-05-18
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] 小脳失調原因蛋白aprataxin導入によるTriple A症候群のストレス起因性細胞死の抑制2007
- Author(s)
  平野牧人, 他4名
- Organizer
  第48回日本神経学会総会
- Place of Presentation
  名古屋
- Year and Date
  2007-05-18
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] ALADLNI482S causes hypersensitivily to oxidative stress by selective failure of DNA repair protein import in triple A syndrome2007
- Author(s)
  Asai H, Hirano M, 他5名
- Organizer
  Neuroscience 2008
- Place of Presentation
  San Diego,USA
- Year and Date
  2007-11-05
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] A Japanese family with triple A syndrome caused by a novel mutation in the ALADIN gene2007
- Author(s)
  Furiya Y, Hirano M, 他5名
- Organizer
  5th Congress of the International Society for Autonomic Neuroscience
- Place of Presentation
  Kyoto, Japan
- Year and Date
  2007-10-07
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] 新たなALADIN遺伝子変異を伴うTriple A症候群における、小脳失調原因蛋白arataxinの核内輸送障害2007
- Author(s)
  浅井宏英、平野牧人, 他3名
- Organizer
  第48回日本神経学会総会
- Place of Presentation
  名古屋
- Year and Date
  2007-05-18
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] Mutant ALADIN responsible for triple A syndrome impairs nuclear import of aprataxin,a DNA repair protein causative for ataxia2007
- Author(s)
  Hirano M, 他5名
- Organizer
  Neuro2007(日本神経化学会総会)
- Place of Presentation
  横浜
- Year and Date
  2007-09-10
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] A Japanese family with triple A syndrome caused by a novel mutation in the ALADIN gene2007
- Author(s)
  Furiya Y, Hirano M, 他5名
- Organizer
  5th Congress of the International Society for Autonomic Neuroscience
- Place of Presentation
  Kyoto,Japan
- Year and Date
  2007-10-07
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] Mutant ALADIN responsible for triple A syndrome impairs nuclear import of aprataxin, a DNA repair protein causative for ataxia2007
- Author(s)
  Hirano M, 他5名
- Organizer
  Neuro2007(日本神経化学会総会)
- Place of Presentation
  横浜
- Year and Date
  2007-09-10
- Data Source
  KAKENHI-PROJECT-19591002
[Presentation] Electrophysiological subtypes of GBS with anti-Gal-C antibodies and other anti-glycolipid antibodies
- Author(s)
  Kusunoki S, Samukawa M, Hamada, Y, Kuwahara M, Takada K, Hirano M, Mitsui Y.
- Organizer
  Inflammatory Neuropathy Consortium
- Place of Presentation
  Dusseldorf, Germany
- Year and Date
  2014-07-12 – 2014-07-16
- Data Source
  KAKENHI-PROJECT-24390225
[Presentation] 多系統萎縮症および常染色体優性遺伝性脊髄小脳変性症におけるCOQ2遺伝子解析 COQ2 gene analyses in multiple system atrophy and dominantly-inherited ataxia
- Author(s)
  平野牧人、中村雄作、阪本　光、上野周一、三井良之、西郷和真、楠　進
- Organizer
  日本神経学会総会
- Place of Presentation
  福岡(福岡国際会議場)
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] Analyses of the COQ2 gene in Japanese patients with multiple system atrophy and other neurodegenerative diseases
- Author(s)
  Makito Hirano, Yusaku Nakamura, Kazumasa Saigoh, Hikaru Sakamoto, Shuichi Ueno, Yoshiyuki Mitsui, Susumu Kusunoki
- Organizer
  Annual Meeting of American Neurological Association
- Place of Presentation
  Baltimore
- Year and Date
  2014-10-12 – 2014-10-14
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] 多系統の障害をきたしたSOD1変異例
- Author(s)
  阪本　光、平野牧人、上野周一、赤松舞子、中村雄作、楠　進
- Organizer
  日本神経学会総会
- Place of Presentation
  福岡(福岡国際会議場)
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] Differential progression of dysphagia between spinocerebeller ataxia type 3 and type 6
- Author(s)
  Chiharu Isono, Makito Hirano, Hikaru Sakamoto, Shuichi Ueno, Susumu Kusunoki, Yusaku Nakamura
- Organizer
  Annual Meeting of American Neurological Association
- Place of Presentation
  Baltimore
- Year and Date
  2014-10-12 – 2014-10-14
- Data Source
  KAKENHI-PROJECT-25461297
[Presentation] Rotigotine transdermal patchにより嚥下機能が著明に改善した誤嚥性肺炎合併パーキンソン病患者の一例
- Author(s)
  平野牧人、磯野千春、上野周一、阪本　光、楠　進、中村雄作
- Organizer
  日本神経治療学会
- Place of Presentation
  東京(東京ドームホテル)
- Year and Date
  2014-11-20 – 2014-11-22
- Data Source
  KAKENHI-PROJECT-25461297
[]

1. UENO Satoshi (40184949)

# of Collaborated Projects: 2 results

# of Collaborated Products: 21 results
2. SAIGOH Kazumasa (50319688)

# of Collaborated Projects: 2 results

# of Collaborated Products: 12 results
3. 竹原俊幸 (60580561)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
4. MORI Toshio (10115280)

# of Collaborated Projects: 1 results

# of Collaborated Products: 8 results
5. KUSUNOKI Susumu (90195438)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
6. MIYAMOTO Katsuichi (50388526)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. TSUBATA Takeshi (80197756)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. MURATA Ken-ya (90264853)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. 美馬達哉 (20324618)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. 小野弓絵 (10360207)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. 野嶌一平 (20646286)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. 桐本光 (40406260)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. 植木美乃 (40467478)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 小金丸聡子 (40579059)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 宇川義一 (50168671)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 福田敦夫 (50254272)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 大須理英子 (60374112)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. 北城圭一 (70302601)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. 竹内雄一 (70588384)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 芝田純也 (70844166)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. MORISE Jyoji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
22. MIYATA Shinji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
23. 岡昌吾

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 井原健二

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 高嶋博

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 橋口昭大

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 村田茂穂

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 田中啓二

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. 北川裕之

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

HIRANO Makito 平野 牧人

平野 政人 ヒラノ マサト

Research Projects

Research Products

Co-Researchers

クローズドループ刺激による非侵襲的Deep Brainリハビリテーションの創生

Principal Investigator

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Review Section

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The clarification of pathomechanism and the establishment of treatment for repeat expansion-associated amyotrophic lateral sclerosisPrincipal Investigator

Principal Investigator

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Review Section

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Identification of proteins associated with ATXN8OS-related amyotrophic lateral sclerosis and treatment of iPS cell modelsPrincipal Investigator

Principal Investigator

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Review Section

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Clarification of pathomechanism via amyotrophic lateral sclerosis-causing ERBB4 and effectiveness of anti-cancer medicine.Principal Investigator

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Therapeutic protein degradation and relationship between p62 and ubiquilin 2, new proteins causative for neurodegenerative diseasesPrincipal Investigator

Principal Investigator

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Analysis of negative regulators of B lymphocyte responses to glycoconjugates in neuroimmunological diseases

Principal Investigator

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Interaction, posttranslational modification, and subcellular localization of proteins causative for neurodegenerative diseasesPrincipal Investigator

Principal Investigator

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Repairing DNA damages in neurodegenerative diseases

Principal Investigator

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Clarification of the link between nuclear import of neurodegenerative disease-causing proteins and the pathomechanismsPrincipal Investigator

Principal Investigator

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Research Institution

遺伝性小脳失調原因遺伝子アプラタキシンの野生型及びスプライス変異型蛋白の機能解析Principal Investigator

Principal Investigator

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Analyses for the function and related gene of humanin that suppresses cell death induced by mutant Alzheimer disease genes

Principal Investigator

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Research Institution

[Book] 脳神経内科疾患の摂食嚥下・栄養ケアハンドブック 患者・家族とケアスタッフのための手引きとQ＆A2023

Author(s)

Total Pages

Publisher

ISBN

Data Source

[Book] 脳神経内科の摂食嚥下障害2018

Author(s)

Total Pages

HIRANO Makito 平野牧人

平野政人ヒラノマサト

[Book] 脳神経内科疾患の摂食嚥下・栄養ケアハンドブック患者・家族とケアスタッフのための手引きとQ＆A2023

[Book] Bardet-Biedl(バルデー・ビードル)症候群(pp495-497)　神経症候群IV2014