YOSHIDA KUNIHIRO 吉田邦広

… Alternative Names

YOSHIDA Kunihiro 吉田邦広

吉田邦広ヨシダクニヒロ

吉田邦弘ヨシダクニヒロ

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Researcher Number	90242693
Other IDs
External Links
Affiliation (Current)	2025: 信州大学, 医学部, 特任教授
Affiliation (based on the past Project Information) *help	2014 – 2018: 信州大学, 医学部, 特任教授 2016: 信州大学, 医学部附属病院, 特任教授 2012 – 2013: 信州大学, 医学部, 教授 2007 – 2009: Shinshu University, 医学系研究科, 准教授 2002: 信州大学, 医学部附属病院・遺伝子診療部, 助教授 … More 2002: SHINSHU UNIVERSITY HOSPITAL, DIVISION OF CLINICAL AND MOLECULAR GENETICS, ASSOCIATE PROFESSOR, 医学部附属病院・遺伝子診療部・副部長助教授 2001: 信州大学, 医学部・附属病院・遺伝子診療部・副部長, 助教授 2000: 信州大学, 医学部・附属病院・遺伝子診療部・副部長助教授 1998: 信州大学, 医学部第三内科, 講師 1997: 信州大学, 医学部・第三内科, 助手 1994: 信州大学, 医学部・附属病院, 助手 Less
Review Section/Research Field	Principal Investigator Neurology / Neurology / Medical systems Except Principal Investigator Neurology / Nerve anatomy/Neuropathology
Keywords	Principal Investigator 脊髄小脳失調症31型 / 脊髄小脳変性症 / harmonic ratio / 神経難病 / 医用ロボット / リハビリテーション / 脳神経疾患 / ロボット工学 / 同調制御法 / 脳卒中 … More / 着脱型ロボット / 歩行アシスト / ASTROCYTE / OXIDATIVE STRESS / IRON METABOLISM / GENE-TARGETING / CERULOPLASMIN / フリーラジカル / 星状膠細胞 / 酸化的ストレス / 鉄代謝 / 遺伝子改変マウス / セルロプラスミン / 繰り返し配列 / 脊髄小脳失調症 / 蛋白-RNA結合 / RNA結合蛋白 / Golgi装置断片化 / プルキンエ細胞 / 一塩基多型 / 遺伝子診断 / 連鎖解析 / 5塩基繰り返し配列 / 挿入変異 / puratrophin-1 / 常染色体優性遺伝 / dystrophinopathy / insertion / L1 element / dystrophin isoform / XLDCM / dystrophin / プロモーター / 転写制御 / 心筋 / 骨格筋 / Myocyte-specific Enhancer 2 / ジストロフィン遺伝子 / ジストロフィン … More Except Principal Investigator マクロファージ / スフェロイド / コロニー刺激因子１受容体 / 白質脳症 / ミクログリア / マクロファージコロニー刺激因子受容体 / 若年性認知症 / 神経軸索スフェロイドを伴う遺伝性び慢性白質脳症 / マクロファージコロニー刺激因子 / 神経軸索ジストロフィー / コロニー刺激因子1受容体 / HDLS / 分子遺伝学 / 神経難病 / 遺伝子 / 神経病理 / 筋萎縮性側索硬化症 / 病理学 / グリア胞体内封入体 / 脳神経疾患 / グリア細胞封入体 / グリア細胞胞体内封入 / 病期分類 / グリア細胞内封入体 / 脊髄小脳変性症 / 多系統萎縮症 Less

Stages of glial inclusion pathology in multiple system pathology
- Principal Investigator
  
  Yamada Mitsunori
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Nerve anatomy/Neuropathology
- Research Institution
  Shinshu University
Application of robotic wear curara for intractable neurodegenerative diseasesPrincipal Investigator
- Principal Investigator
  
  Yoshida Kunihiro
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Medical systems
- Research Institution
  Shinshu University
Gene analysis and clinicopathological features of amyotrophic lateral sclerosis in the area where there are many patients
- Principal Investigator
  
  HINENO Akiyo
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Shinshu University
A study of the pathomechanism in early-onset dementia due to macrophage colony stimulating factor receptor gene mutations.
- Principal Investigator
  
  FUKUSHIMA Kazuhiro
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neurology
- Research Institution
  Shinshu University
Proteome analysis for spinocerebellar ataxia type 31Principal Investigator
- Principal Investigator
  
  YOSHIDA Kunihiro
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Shinshu University
Research on 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA)Principal Investigator
- Principal Investigator
  
  YOSHIDA Kunihiro
- Project Period (FY)
  2007 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Shinshu University
RESEARCH ON THE PATHOGENESIS AND PATHOPHYSIOLOGY OF HEREDITARY CERULOPLASMIN DEFICIENCY (ACERULOPLASMINEMIA)Principal Investigator
- Principal Investigator
  
  YOSHIDA Kunihiro
- Project Period (FY)
  2000 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  SHINSHU UNIVERSITY
伴性劣性遺伝型拡張型心筋症の病因,病態に関する分子生物学的研究Principal Investigator
- Principal Investigator
  
  吉田邦広 (吉田邦弘)
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Neurology
- Research Institution
  Shinshu University
骨格筋および心筋におけるジストロフィン遺伝子の発現調節に関する分子生物学的研究Principal Investigator
- Principal Investigator
  
  吉田邦広
- Project Period (FY)
  1993 – 1994
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Neurology
- Research Institution
  Shinshu University

All 2018 2017 2016 2015 2014 2013 2012 2010 2009 2008 2007 Other

All Journal Article Presentation Book

[Book] 孤発性皮質性小脳萎縮症. 神経症候群（第2版）―その他の神経疾患を含めて―. II　III　変性疾患（脊髄小脳変性症, 孤発性脊髄小脳変性症）（新領域別症候群シリーズNo.27）2014
- Author(s)
  吉田邦広（分担）
- Total Pages
  903
- Publisher
  日本臨床社
- Data Source
  KAKENHI-PROJECT-24591255
[Journal Article] Effect of the synchronization-based control of a wearable robot having a non-exoskeletal structure on the hemiplegic gait of stroke patients.2018
- Author(s)
  Mizukami N, Takeuchi S, Tetsuya M, Tsukahara A, Hashimoto M, Yoshida K, Matsushima A, Maruyama Y, Tako K.
- Journal Title
  
  IEEE Trans Neural Syst Rehabil Eng
  
  Volume: 26 Issue: 5 Pages: 1011-1016
- DOI
  10.1109/tnsre.2018.2817647
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H03031
[Journal Article] Principal component analysis for ataxic gait using a triaxial accelerometer.2017
- Author(s)
  Matsushima A, Yoshida K, Genno H, Ikeda S.
- Journal Title
  
  J NeuroEng Rehabili
  
  Volume: 14 Issue: 1 Pages: 37-37
- DOI
  10.1186/s12984-017-0249-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H03031
[Journal Article] Natural history of spinocerebellar ataxia type 31: a 4-year prospective study.2017
- Author(s)
  Nakamura K, Yoshida K, Matsushima A, Shimizu Y, Sato S, Yahikozawa H, Ohara S, Yazawa m, Ushiyama M, Sato M, Morita H, Inoue A, Ikeda S.
- Journal Title
  
  The Cerebellum
  
  Volume: 16 Issue: 2 Pages: 518-524
- DOI
  10.1007/s12311-016-0833-6
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15H03031
[Journal Article] ロボティックウエアcuraraの実用化に向けた取り組み2016
- Author(s)
  吉田邦広、橋本稔
- Journal Title
  
  Medical Science Digest
  
  Volume: 42 Pages: 618-622
- Data Source
  KAKENHI-PROJECT-15H03031
[Journal Article] Elevation of serum heat-shock protein levels in amyotrophic lateral sclerosis2016
- Author(s)
  Miyazaki D, Nakamura A, Hineno A, Kobayashi C, Kinoshita T, Yoshida K, Ikeda SI.
- Journal Title
  
  Neurol Sci
  
  Volume: 印刷中
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461274
[Journal Article] Lower urinary tract dysfunction and neuropathological findings of the neural circuits controlling micturition in familial amyotrophic lateral sclerosis with L106V mutation in the <i>SOD1</i> gene2016
- Author(s)
  日根野晃代, 小栁清光, 中村昭則, 下島吉雄, 吉田邦広, 池田修一
- Journal Title
  
  Rinsho Shinkeigaku
  
  Volume: 56 Issue: 2 Pages: 69-76
- DOI
  10.5692/clinicalneurol.cn-000767
- NAID
  130005132720
- ISSN
  0009-918X, 1882-0654
- Language
  Japanese
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25461274
[Journal Article] Shinshu Brain Resource Net2016
- Author(s)
  Oyanagi K, Yamada M, Hineno A, Yahikozawa H, Ushiyama M, Miki J, Kanno H, Nakayama J, Makishita H, Inoue K, Ohara S, Hayashida K, Kayanuma K, Yamamoto K, Yasude T, Hashimoto T, Yoshida K, Ikeda SI
- Journal Title
  
  Neuropathology
  
  Volume: 36 Issue: 6 Pages: 600-601
- DOI
  10.1111/neup.12304
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25461274
[Journal Article] Elevation of serum heat-shock protein levels in amyotrophic lateral sclerosis2016
- Author(s)
  Miyazaki D, Nakamura A, Hineno A, Kobayashi C, Kinoshita T, Yoshida K, Ikeda SI
- Journal Title
  
  Neurol Sci
  
  Volume: 37 Issue: 8 Pages: 1277-1281
- DOI
  10.1007/s10072-016-2582-1
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25461274
[Journal Article] Rare frequency of downbeat positioning nystagmus in spinocerebellar ataxia type 31.2015
- Author(s)
  Yabe I, Matsushima M, Yoshida K, Ishikawa K, Shirai S, Takahashi I, Sasaki H.
- Journal Title
  
  J Neurol Sci.
  
  Volume: Mar 15;350(1-2) Issue: 1-2 Pages: 90-92
- DOI
  10.1016/j.jns.2014.12.042
- NAID
  120005722547
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591252, KAKENHI-PROJECT-24591255, KAKENHI-PUBLICLY-25129703
[Journal Article] Predominant cerebellar phenotype in spastic paraplegia 7 (SPG7).2015
- Author(s)
  Yahikozawa H, Yoshida K, Shunichi S, Hanyu N, Doi H, Miyatake S, Matsumoto N.
- Journal Title
  
  Human Genome Variation
  
  Volume: 2 Issue: 1 Pages: 15015-15015
- DOI
  10.1038/hgv.2015.12
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591255, KAKENHI-PROJECT-26461549, KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118007
[Journal Article] Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer.2015
- Author(s)
  Matsushima A, Yoshida K, Genno H, Murata A, Matsuzawa S, Nakamura K, Nakamura A, Ikeda S.
- Journal Title
  
  Cerebellum Ataxias
  
  Volume: 2 Issue: 1 Pages: 9-9
- DOI
  10.1186/s40673-015-0028-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H03031
[Journal Article] A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan.2014
- Author(s)
  Yasui K, Yabe I, Yoshida K, Kanai K, Arai K, Ito M, Onodera O, Koyano S, Isozaki E, Sawai S, Adachi Y, Sasaki H, Kuwabara S, Hattori T, Sobue G, Mizusawa H, Tsuji S, Nishizawa M, Nakashima K.
- Journal Title
  
  Orphanet Jounal of Rare Diseases
  
  Volume: 9 Issue: 1 Pages: 118-118
- DOI
  10.1186/s13023-014-0118-4
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591255, KAKENHI-PROJECT-26460907, KAKENHI-PROJECT-26461319
[Journal Article] Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.2014
- Author(s)
  Yoshida K, Asakawa M, Suzuki-Kouyama E, Tabata K, Shintaku M, Ikeda S, Oyanagi K.
- Journal Title
  
  Neuropathology
  
  Volume: 印刷中 Issue: 3 Pages: 261-267
- DOI
  10.1111/neup.12090
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591255
[Journal Article] ‘Cortical cerebellar atrophy’ dwindles away in the era of next-generation sequencing.2014
- Author(s)
  Yoshida K, Miyatake S, Kinoshita T, Doi H, Tsurusaki Y, Miyake N, Saitsu H, Matsumoto N.
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 59 Issue: 10 Pages: 589-590
- DOI
  10.1038/jhg.2014.75
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591255, KAKENHI-PROJECT-25293235, KAKENHI-PROJECT-25860915, KAKENHI-PROJECT-26461549
[Journal Article] Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation2014
- Author(s)
  Doi H, Ushiyama M, Baba T, Tani K, Shiina M, Ogata K, Miyatake S, Yuzawa YF, Tsuji S, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Ikeda S, Tanaka F, Matsumoto N, Yoshida K
- Journal Title
  
  Sci Rep
  
  Volume: 4 Issue: 1 Pages: 7132-7132
- DOI
  10.1038/srep07132
- NAID
  120007100602
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22129005, KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118005, KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-24249019, KAKENHI-PROJECT-24591255, KAKENHI-PROJECT-25293207, KAKENHI-PROJECT-25293235, KAKENHI-PROJECT-25461287, KAKENHI-PROJECT-26330331, KAKENHI-PROJECT-26440105, KAKENHI-PROJECT-26461549, KAKENHI-PROJECT-26670445
[Journal Article] リピート伸長病（repeat expansion disease）―トリプレットリピート病を中心に―2012
- Author(s)
  吉田邦広
- Journal Title
  
  SRL宝函
  
  Volume: 32 Pages: 20-29
- Data Source
  KAKENHI-PROJECT-24591255
[Journal Article] 皮質性小脳萎縮症（CCA）2012
- Author(s)
  吉田邦広
- Journal Title
  
  最新医学
  
  Volume: 67 Pages: 1071-1076
- Data Source
  KAKENHI-PROJECT-24591255
[Journal Article] Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan.2010
- Author(s)
  Sakai H, Yoshida K, Shimizu Y, et al.(計6名)
- Journal Title
  
  Neurogenetics (in press)
- NAID
  120007110502
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA)in the endemic Nagano area of Japan.2009
- Author(s)
  Yoshida K, Shimizu Y, Morita H, et al.
- Journal Title
  
  Cerebellum 8
  
  Pages: 46-51
- NAID
  120007110508
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Spinocerebellar ataxia type 6 (SCA6) : Clinical pilot trial with gabapentin. 278 : 107-111, 2009.2009
- Author(s)
  Nakamura K, Yoshida K, Miyazaki D, Morita H, Ikeda S.
- Journal Title
  
  J Neurol Sci 278
  
  Pages: 107-111
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Spinocerebellar ataxia type 6(SCA6) : Clinical pilot trial with gabapentin.2009
- Author(s)
  Nakamura K, Yoshida K, Miyazaki D, et al.(計5名)
- Journal Title
  
  J Neurol Sci 278
  
  Pages: 107-111
- NAID
  120007110528
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Severity and progression rate of cerebellar ataxia in 16q-linkedautosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano area of Japan.2009
- Author(s)
  Yoshida K, Shimizu Y, Morita H, et al. (計17名)
- Journal Title
  
  Cerebellum 8
  
  Pages: 46-51
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia(16q-ADCA)in the endemic Nagano area of Japan.2009
- Author(s)
  Yoshida K, Shimizu Y, Morita H, et al.(計17名)
- Journal Title
  
  Cerebellum 8
  
  Pages: 46-51
- NAID
  120007110508
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Spinocerebellar ataxia type 6 (SCA6): Clinical pilot trial with gabapentin.2009
- Author(s)
  Nakamura K, Yoshida K, Miyazaki D, et al. (計5名)
- Journal Title
  
  J Neurol Sci 278
  
  Pages: 107-111
- NAID
  120007110528
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2).2009
- Author(s)
  Nakamura K, Yoshida K, Makishita H, et al. (計6名)
- Journal Title
  
  J Hum Genet 54
  
  Pages: 746-748
- NAID
  10030732987
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2(AOA2).2009
- Author(s)
  Nakamura K, Yoshida K, Makishita H, et al.(計6名)
- Journal Title
  
  J Hum Genet 54
  
  Pages: 746-748
- NAID
  10030732987
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Increased vulnerability to rotenone-induced neurotoxity in ceruloplasimin-deficient mice.2008
- Author(s)
  Kaneko K, Hineno A, Yoshida K, Ikeda S.
- Journal Title
  
  Neurosci Lett 446
  
  Pages: 56-58
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Congenital fibrosis of the extraocular muscles(CFEOM)syndrome as sociated with progressive cerebellar ataxia2007
- Author(s)
  Yoshida K, Okano T, Hoshi K, et. al.
- Journal Title
  
  Am J Med Genet 143A
  
  Pages: 1494-1501
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan.2007
- Author(s)
  Yoshida K, Wada T, Sakurai A, et al. (計6名)
- Journal Title
  
  J Hum Genet 52
  
  Pages: 675-679
- NAID
  10019812864
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan.2007
- Author(s)
  Yoshida K, Wada T, Sakurai A, et. al.
- Journal Title
  
  J Hum Genet 52
  
  Pages: 675-679
- NAID
  10019812864
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Congenital fibrosis of the extraocular muscles (CFEOM) syndrome associated with progressive cerebellar ataxia.2007
- Author(s)
  Yoshida K, Okano T, Hoshi K, et al. (計9名)
- Journal Title
  
  Am J Med Genet 143A
  
  Pages: 1494-1501
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Journal Article] Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano
- Author(s)
  Sakai H, Yoshida K, Shimizu Y, et al. (計6名)
- Journal Title
  
  Japan. Neurogenetics (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 脊髄小脳変性症：診療と研究のクロストーク.2017
- Author(s)
  吉田邦広
- Organizer
  第13回阪神SCDセミナー
- Place of Presentation
  尼崎（都ホテルニューアルカイック）
- Year and Date
  2017-02-03
- Invited
- Data Source
  KAKENHI-PROJECT-15H03031
[Presentation] Evaluation of walking smoothness using wearable robotic system curara® for spinocerebellar degeneration patients.2017
- Author(s)
  Tsukahara A, Yoshida K, Matsushima A, Ajima K, Kuroda C, Mizukami N, Hashimoto M.
- Organizer
  15th International Conference on Rehabilitation Robotics 2017 (ICORR2017)
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H03031
[Presentation] Gait analysis in SCA6 and SCA31 with a triaxial accelerometer.2017
- Author(s)
  Matsushima A, Yoshida K, Genno H, Ikeda S.
- Organizer
  XXIII World Congress of Neurology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H03031
[Presentation] 片麻痺患者のリハビリ訓練におけるロボティックウェアcurara®の同調制御法の効果.2016
- Author(s)
  水上憲明, 竹内志津江, 鉄矢美紀雄, 塚原淳, 橋本稔, 吉田邦広, 松嶋聡, 丸山陽一, 田幸健司.
- Organizer
  第6回日本ロボットリハビリテーション・ケア研究会in HYOGO.
- Place of Presentation
  神戸（兵庫県立総合リハビリテーションセンター）
- Year and Date
  2016-11-12
- Data Source
  KAKENHI-PROJECT-15H03031
[Presentation] Measuring the severity of ataxia using a triaxial accelerometer. A new assessment method.2016
- Author(s)
  Matsushima A, Yoshida K, Genno H, Matsuzawa S, Ikeda S.
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  神戸（神戸国際会議場）
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-15H03031
[Presentation] ロボティックウェアcuraraによる脊髄小脳変性症患者のための歩行支援.2016
- Author(s)
  所宏美、塚原淳, 吉田邦広, 松嶋聡, 中村勝哉, 橋本稔.
- Organizer
  日本機械学会ロボティクス・メカトロニクス講演会2016
- Place of Presentation
  横浜（パシフィコ横浜）.
- Year and Date
  2016-06-08
- Data Source
  KAKENHI-PROJECT-15H03031
[Presentation] 3軸加速度計を用いた失調性歩行の定量的な解析と評価法への応用.2016
- Author(s)
  松嶋聡, 吉田邦広, 源野広和, 江澤直樹, 池田修一.
- Organizer
  第34回日本神経治療学会総会
- Place of Presentation
  米子（米子コンベンションセンターBiG SHiP, 米子市文化ホール）
- Year and Date
  2016-11-03
- Data Source
  KAKENHI-PROJECT-15H03031
[Presentation] ロホティックウェア curara による脊髄小脳変性症患者のための歩行支援2015
- Author(s)
  所宏美、塚原淳、吉田邦広、松嶋聡、中村勝哉、橋本稔
- Organizer
  日本機械学会ロボティクス・メカトロニクス部門
- Place of Presentation
  パシフィコ横浜（神奈川県・横浜市）
- Year and Date
  2015-06-08
- Data Source
  KAKENHI-PROJECT-15H03031
[Presentation] 腫大軸索を伴う遺伝性びまん性白質脳症(HDLS)患者の単球由来マクロファージの検討2014
- Author(s)
  福島和広, 近藤恭史, 松嶋聡, 木下通亨, 星研一, 矢彦沢裕之, 吉田邦広, 池田修一
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡国際会議場
- Data Source
  KAKENHI-PROJECT-25860704
[Presentation] 脊髄小脳失調症31型の小脳プルキンエ細胞の形態変化とゴルジ装置断片化の検討2014
- Author(s)
  吉田邦広, 浅川美果, 鈴木絵美, 田畑賢一, 新宅雅幸, 池田修一, 小栁清光.
- Organizer
  第55回日本神経病理学会総会学術研究会
- Place of Presentation
  学術総合センター（一橋構堂）（東京都千代田区）
- Data Source
  KAKENHI-PROJECT-24591255
[Presentation] 腰髄に巣状の脊髄神経細胞脱落と皮質脊髄路変性を認めたポリオ後症候群の１剖検例2013
- Author(s)
  日根野晃代，中村卓也，吉田拓弘，酒井康弘，菅野祐幸，小栁清光, 池田修一
- Organizer
  第54回神経病理学会
- Place of Presentation
  タワーホテル船堀
- Data Source
  KAKENHI-PROJECT-25461274
[Presentation] 軸索腫大と伴う遺伝性びまん性白質脳症のSPECT所見とその神経病理学的背景2013
- Author(s)
  吉田邦広、木下朋実、近藤泰史、木下通亨、福島和広、浅川美果、鈴木絵美、上原弥生、池田修一、小栁清光
- Organizer
  第32回日本認知症学会
- Place of Presentation
  キッセイ文化ホール
- Data Source
  KAKENHI-PROJECT-25860704
[Presentation] 神経難病患者診療におけるモバイル電子端末を用いた在宅チームケアシステムの有用性2013
- Author(s)
  日根野晃代，中村昭則，松沢由美，両角由里，滝沢正臣，吉田邦広，池田修一
- Organizer
  第54回日本神経学会学術大会
- Place of Presentation
  東京国際フォーラム
- Data Source
  KAKENHI-PROJECT-25461274
[Presentation] 腫大軸索を伴う遺伝性白質脳症（HDLS）剖検脳を用いたCSF-1Rシグナル伝達分子の検討2013
- Author(s)
  福島和広, 近藤恭史, 木下通亨, 吉田邦広, 矢澤生, 小栁清光, 池田修一
- Organizer
  第54回日本神経学会学術大会
- Place of Presentation
  東京国際フォーラム
- Data Source
  KAKENHI-PROJECT-25860704
[Presentation] 脊髄小脳失調症31型小脳病変の神経病理学的再検討2013
- Author(s)
  吉田邦広, 浅川美果, 鈴木絵美, 田畑賢一, 新宅雅幸, 池田修一, 小栁清光.
- Organizer
  第54回日本神経学会学術大会
- Place of Presentation
  東京国際フォーラム（東京都千代田区）
- Data Source
  KAKENHI-PROJECT-24591255
[Presentation] 脊髄小脳失調症31型小脳病変の神経病理学的再検討2013
- Author(s)
  吉田邦広, 浅川美果, 鈴木絵美, 田畑賢一, 新宅雅幸, 池田修一, 小栁清光.
- Organizer
  第54回日本神経学会学術大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24591255
[Presentation] 脊髄小脳失調症31型における(TGGAA)n・(UGGAA)n結合蛋白の探索2012
- Author(s)
  吉田邦広, 鈴木佳代, 石川えり, 小栁清光, 池田修一.
- Organizer
  第53回日本神経学会学術大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24591255
[Presentation] 純粋小脳型脊髄小脳変性症における臨床像と脳血流シンチグラフィの検討.2009
- Author(s)
  清水雄策, 吉田邦広, 安出卓司, ら.(計5名)
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-22
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 純粋小脳型脊髄小脳変性症における臨床像と脳血流シンチグラフィの検討2009
- Author(s)
  清水雄策, 吉田邦広, 安出卓司, (他2名)
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-22
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 末梢神経障害を伴った脊髄小脳変性症(SCD)患者の臨床像.2009
- Author(s)
  中村勝哉, 吉田邦広, 関島良樹, ら.(計8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-19590985
[Presentation] 脊髄小脳変性症の臨床-診断・治療の実際-2009
- Author(s)
  吉田邦広
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-20
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 脊髄小脳失調症6型(SCA6)に対するガバペンチン療法2008
- Author(s)
  中村勝哉, 吉田邦広, 宮崎大吾, (他2名)
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  横浜
- Year and Date
  2008-05-15
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 脊髄小脳失調症6型(SCA6)に対するガバペンチン療法2008
- Author(s)
  中村勝哉, 吉田邦広, 宮崎大吾, (他2名)
- Organizer
  第105回日本内科学会講演会
- Place of Presentation
  東京
- Year and Date
  2008-04-11
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 脊髄小脳失調症6型(SCA6)に対するガバペンチン療法.2008
- Author(s)
  中村勝哉, 吉田邦広, 宮崎大吾, 森田洋, 池田修一.
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  横浜
- Year and Date
  2008-05-15
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 16番染色体長腕に連鎖する優性遺伝性脊髄小脳変性症(16q-ADCA)の自然史2008
- Author(s)
  吉田邦広, 清水雄策, 森田洋, (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-19590985
[Presentation] 脊髄小脳失調症6型の自然史-多施設共同後ろ向き調査-.2008
- Author(s)
  安井建一, 矢部一郎, 佐々木秀直, 新井公人, 金井数明, 服部孝道, 吉田邦広, 磯崎英治, 小野寺理, 西澤正豊, 中島健二.
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  横浜
- Year and Date
  2008-05-15
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 脊髄小脳失調症6型(SCA6)に対するガバペンチン療法.2008
- Author(s)
  中村勝哉, 吉田邦広, 宮崎大吾, 森田洋, 池田修一.
- Organizer
  第105回日本内科学会講演会
- Place of Presentation
  東京
- Year and Date
  2008-04-11
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 16番染色体長腕に連鎖する優性遺伝性脊髄小脳変性症(16q-ADCA)の自然史.2008
- Author(s)
  吉田邦広, 清水雄策, 森田洋, 中村勝哉, 田澤浩一, 岡野友美, 大原慎司, 井上敦, 田畑賢一, 佐藤俊一, 池田修一.
- 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-19590985
[Presentation] 16番染色体長腕に連鎖する優性遺伝性脊髄小脳変性症の病因解析2007
- Author(s)
  吉田邦広, 堺温哉, 大畑尚子, (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-19590985
[Presentation] puratrophin-1遺伝子-16C>T置換陽性患者の臨床像に関する検討2007
- Author(s)
  清水雄策, 吉田邦広, 岡野友美, (他1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-19590985
[Presentation] 長野県の原因遺伝子未同定SCA患者におけるSCA14遺伝子異常の検討2007
- Author(s)
  岡野友美, 吉田邦広, 清水雄策, (他2名)
- Organizer
  第48回日本神経学会総会
- Place of Presentation
  名古屋
- Year and Date
  2007-05-16
- Data Source
  KAKENHI-PROJECT-19590985
[Presentation] 脊髄小脳失調症31型の小脳プルキンエ細胞の形態変化とゴルジ装置断片化の検討.
- Author(s)
  吉田邦広, 浅川美果, 鈴木－香山絵美, 田畑賢一, 新宅雅幸, 池田修一, 小栁清光.
- Organizer
  第55回日本神経病理学会総会学術研究会
- Place of Presentation
  東京（学術総合センター）
- Year and Date
  2014-06-05 – 2014-06-07
- Data Source
  KAKENHI-PROJECT-24591255
[Presentation] 小脳失調症のリズム解析評価の試み（第2報）.
- Author(s)
  安井建一, 田尻佑喜, 吉田邦広, 中島健二.
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡（福岡国際会議場、福岡サンパレス、福岡国際センター）
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-24591255
[Presentation] 脊髄小脳失調症31型の自然史
- Author(s)
  中村勝哉, 吉田邦広, 清水雄策, 兼子一真, 佐藤俊一, 矢彦沢裕之, 森田洋, 大原慎司, 矢沢正信, 牛山雅夫, 佐藤充人, 宮崎大吾, 井上敦, 池田修一.
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡（福岡国際会議場、福岡サンパレス、福岡国際センター）
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-24591255

1. IKEDA Shu-ichi (60135134)

# of Collaborated Projects: 2 results

# of Collaborated Products: 10 results
2. OYANAGI Kiyomitsu (00134958)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
3. 中村昭則 (10303471)

# of Collaborated Projects: 2 results

# of Collaborated Products: 8 results
4. MATSUMOTO Naomichi (80325638)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. TAKEDA Shin'ichi (90171644)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. Yamada Mitsunori (30240039)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. HINENO Akiyo (20596366)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
8. FUKUSHIMA Kazuhiro (10421835)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
9. 橋本稔 (60156297)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
10. 柿田明美 (80281012)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. Tada Mari

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. Toyoshima Yasuko

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. KINOSHITA Michiaki

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
14. KONDO Yasufumi

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
15. MATSUSHIMA Akira

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
16. TANAKA Fumiaki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
17. 石川欽也

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. 土井宏

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

YOSHIDA KUNIHIRO 吉田 邦広

YOSHIDA Kunihiro 吉田 邦広

吉田 邦広 ヨシダ クニヒロ

吉田 邦弘 ヨシダ クニヒロ

Research Projects

Research Products

Co-Researchers

Stages of glial inclusion pathology in multiple system pathology

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Application of robotic wear curara for intractable neurodegenerative diseasesPrincipal Investigator

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Gene analysis and clinicopathological features of amyotrophic lateral sclerosis in the area where there are many patients

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A study of the pathomechanism in early-onset dementia due to macrophage colony stimulating factor receptor gene mutations.

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Proteome analysis for spinocerebellar ataxia type 31Principal Investigator

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Research on 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA)Principal Investigator

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RESEARCH ON THE PATHOGENESIS AND PATHOPHYSIOLOGY OF HEREDITARY CERULOPLASMIN DEFICIENCY (ACERULOPLASMINEMIA)Principal Investigator

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伴性劣性遺伝型拡張型心筋症の病因,病態に関する分子生物学的研究Principal Investigator

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骨格筋および心筋におけるジストロフィン遺伝子の発現調節に関する分子生物学的研究Principal Investigator

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[Book] 孤発性皮質性小脳萎縮症. 神経症候群（第2版）―その他の神経疾患を含めて―. II III 変性疾患（脊髄小脳変性症, 孤発性脊髄小脳変性症）（新領域別症候群シリーズNo.27）2014

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[Journal Article] Effect of the synchronization-based control of a wearable robot having a non-exoskeletal structure on the hemiplegic gait of stroke patients.2018

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[Journal Article] Principal component analysis for ataxic gait using a triaxial accelerometer.2017

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[Journal Article] Natural history of spinocerebellar ataxia type 31: a 4-year prospective study.2017

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YOSHIDA KUNIHIRO 吉田邦広

YOSHIDA Kunihiro 吉田邦広

吉田邦広ヨシダクニヒロ

吉田邦弘ヨシダクニヒロ

[Book] 孤発性皮質性小脳萎縮症. 神経症候群（第2版）―その他の神経疾患を含めて―. II　III　変性疾患（脊髄小脳変性症, 孤発性脊髄小脳変性症）（新領域別症候群シリーズNo.27）2014