TACHI Nobutada 舘延忠

… Alternative Names

館延忠タチノブタダ

舘延忠タチノブタダ

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Researcher Number	80136944
Other IDs
External Links
Affiliation (based on the past Project Information) *help	2010 – 2012: 札幌医科大学, 保健医療学部, 准教授 1999 – 2006: 札幌医科大学, 保健医療学部, 助教授 1995: School of Health Sciences, Sapporo Medical University, Assistant Professor, 保健医療学部, 助教授 1995: School of Health Sciences, Sapporo Medical Univ.Associate Professor, 医学部, 講師 1994 – 1995: 札医大, 医学部, 講師 1994: 札幌医科大学, 保険医療学部, 助教授 1993: 札幌医科大学, 保健医療学部, 助教授
Review Section/Research Field	Principal Investigator Pediatrics / Pediatrics Except Principal Investigator Dermatology / 広領域
Keywords	Principal Investigator SMARD1 / aprataxin / Aprataxin gene / AOA / EOCA-HA / 遺伝子導入 / Adenovirus vector / Cultured peripheral nerve / IGHMBP2 gene / 培養ラツト神経細胞 … More / 983delAAGAA IGHMBP2 cDNA / SMARD 1 / 培養ラット神経細胞 / 変異IGHMBP2 cDNA / IGHMBP2遺伝子 / axonal degeneration / cultured rat peripherl nerve / 689 ins T c DNA / 689insT / aprataxin cDNA / 軸策変性 / 培養ラツト末鞘神経 / 変異aprataxin cDFNA導入 / 軸索変性 / 培養ラット末梢神経 / 変異aprataxin cDNMA導入 / AOA1 gene / FLJ20157 / myelination / constructed adenovirus vector / Mutated Po cDNA / ラツト末梢神経 / 変異Po cDNA / ラット末梢神経 / 変異PocDNA / Myotonic dystrophy protein kinase / DNA diagnosis / Congenital myotonic dystrophy / unstable DNA / 遺伝子診断 / 先天性筋緊張性ジストロフィー症 / 培養筋 / 筋細胞膜 / 筋紡錘 / 神経筋接合部 / 合成ポリペプチド / DM Kinase / MT-PK mRNA / RT-PCR / 遺伝子 / meiotic instability / CTG repeat / 伝子診断 / 先天性筋緊張性ジストロフィー / Real-time PCE / SMN2 cDNAコピー数 / 塩酸アマンタジン / VPA / 培養皮膚線維芽細胞 / SMN2mRNA / 脊髄性筋委縮症 / NMD / SMN蛋白 / SMN2転写産物 / SMN1転写産物 / SMA 複合ヘテロ / 分子遺伝 / 小児神経学 … More Except Principal Investigator XP-A / DNA diagnosis / Adenovirus vector / Complementation group / Xeroderma pigmentosum / 組み換えアデノウイルス / 遺伝子診断 / アデノウイルスベクター / 相補群 / 色素性乾皮症 / P2 protein / Dejerine-Sottas disease / connexin 32 / P0 protein / Schwann cell / Myelin / Peripheral Nerve / hereditary neuropathy / 圧迫麻痺性遺伝性ニューロパチー(HNPP) / 先天性低ミエリン形成性ニューロパチー(CHN) / 遺伝性圧脆弱性ニューロパチー(HNPP) / Connexin32 / Charcot-Marie-Tooth病 / PMP22蛋白 / PASII / P2蛋白 / Dejerine-Sottas病 / コネキシン32 / PO蛋白 / シュワン細胞 / ミエリン / 末梢神経 / 遺伝性ニューロパチー Less

Treatment of sodium valproate and amantazine hydrochloride in spinal muscular atrophyPrincipal Investigator
- Principal Investigator
  
  TACHI Nobutada
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Sapporo Medical University
Analysis of peripheral neuropathy in rat cultured nerve introduced mutant IGHMBP2 cDNA.Principal Investigator
- Principal Investigator
  
  TACHI Nobutada
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Sapporo Medical University
Establishment of complementation group diagnosis of xeroderma pigmentosum by using adenovirus vector
- Principal Investigator
  
  YAMASHITA Toshiharu
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Sapporo Medical University
Axonal degeneration of rat culured nerve introduced mutant aprata in cDNAPrincipal Investigator
- Principal Investigator
  
  TACHI Nobutada
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Sapporo Medical University
Identity of hereditary cerebellar ataxia, peripheral neuropathy, and hypoalbuminemiaPrincipal Investigator
- Principal Investigator
  
  TACHI Nobutada
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Sapporo Medical University
Myelination in cultured rat peripheral nerve inducted mutant Po c DNA.Principal Investigator
- Principal Investigator
  
  TACHI Nobutada
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  School of Health Sciences, Sapporo Medical University
Molecular and patho-physiological atudies on hereditary neuropathy.
- Principal Investigator
  
  UYEMURA Keiichi
- Project Period (FY)
  1994 – 1995
- Research Category
  
  Grant-in-Aid for Co-operative Research (A)
- Research Field
  
  広領域
- Research Institution
  Keio University
DNA diagnosis of congenital myotonic dystrophyPrincipal Investigator
- Principal Investigator
  
  TACHI Nobutada
- Project Period (FY)
  1993 – 1995
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Sapporo Mecial University

All 2013 2012 2011 2010 2006 2005 2003

All Journal Article Presentation

[Journal Article] ラモトリギンの長期使用例の経験2012
- Author(s)
  二階堂弘輝, 舘延忠, 他
- Journal Title
  
  小児科臨床
  
  Volume: 65 Pages: 107-14
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] A myotonic dystrophy 1 patient complicated with placental adherence after miscarriage of one dichorionic diamniotic twin following her tenth in vitro fertilization and embryotransfer2012
- Author(s)
  Endo T, Baba T, Sugio A, Morishita M, Takahashi M, Akashi Y, Ishioka S, Tachi N
- Journal Title
  
  Arch Gynecol Obstet
  
  Volume: 286 Pages: 1605-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] A new mutation of GCH1 in triplets family with dopa-responsive dystonia2011
- Author(s)
  Tachi N, Takahashi S, Jo M, Shinoda M
- Journal Title
  
  Eur J Neurol
  
  Volume: 18 Pages: 1191-3
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] A new mutation of GCH1 in triplets family with dopa-responsive dystonia2011
- Author(s)
  Tachi N, Takahashi S, Jo M, et al
- Journal Title
  
  Eu J Neurol
  
  Volume: 18 Pages: 1191-1193
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] Aprataxin遺伝子変異(689insT)が培養ラツト後根神経節の髄鞘形成に及ぼす影響について2011
- Author(s)
  堀本佳誉、菊池真、舘延忠、他
- Journal Title
  
  札幌医科大学保健医療学部紀要
  
  Volume: 13 Pages: 21-23
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] Aprataxin遺伝子変異(689insT)が培養ラツト後根神経節の髄鞘形成に及ぼす影響について2011
- Author(s)
  堀本佳誉、菊池真、舘延忠, ら
- Journal Title
  
  札幌医科大学保健医療学部紀要
  
  Volume: 13 Pages: 21-27
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] 髄鞘形成期おける初代培養ラツト後根神経節細胞への組み換えアデノウイルスを用いた変異MPZ cDNAの導入2011
- Author(s)
  菊池真、小塚直樹、舘延忠、他
- Journal Title
  
  札幌医科大学保健医療学部紀要
  
  Volume: 13 Pages: 13-20
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] New mutation of CACNA1A gene in episodic ataxia type 22011
- Author(s)
  Nikaido K, Tachi N, Ohya K, Wada T, Tsutsumi H
- Journal Title
  
  Pediatr Int
  
  Volume: 53 Pages: 415-6
- NAID
  10029558653
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] 髄鞘形成期における初代培養ラツト後根神経節細胞への組み換えアデノウイルスを用いた変異MPZ cDNAの導入2011
- Author(s)
  菊池真、小塚直樹、舘延忠, ら
- Journal Title
  
  札幌医科大学保健医療学部紀要
  
  Volume: 13 Pages: 13-20
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] The acid-sensing ion channel 2 (ASIC2) of ciliated cells in the developing rat nasal septum2010
- Author(s)
  Kikuchi S, Ninomiya T, Kawamata T, Ogasawara N, Kojima T, Tachi N, et al
- Journal Title
  
  Arch Histol Cytol
  
  Volume: 73 Pages: 81-89
- NAID
  10028160137
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591133
[Journal Article] Walker-Warburg症候群と鑑別を要した福山型先天性筋ジストロフィーの1例.2006
- Author(s)
  加藤高広, 舘延忠ら
- Journal Title
  
  臨床小児医学 54
  
  Pages: 17-20
- NAID
  40007293283
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] ウイリアムズ症候群児における視空間情報処理過程の特徴.2006
- Author(s)
  本間朋恵, 舘延忠ら
- Journal Title
  
  作業療法 25
  
  Pages: 116-123
- NAID
  10018140282
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] 筋緊張性ジストロフィー症における3塩基反復配列(CTGリピート)数と2005
- Author(s)
  菊池真, 舘延忠, 小塚直樹他
- Journal Title
  
  総合リハ 33
  
  Pages: 167-173
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] Clinicopathological and virological analyses of familial humanT-lymphotropic virus type I-associated polyneuropathy.2005
- Author(s)
  Sawa H, Tachi N et al.
- Journal Title
  
  J Neurovirol 11
  
  Pages: 199-207
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] Clinicopathological and virological analyses of familial human T-lymphotropic virus type I-associated polyneuropathy.2005
- Author(s)
  Sawa H, Nagashima K, Tachi N, et al.
- Journal Title
  
  J Neurovirol 11
  
  Pages: 199-207
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] A new mutation of IGHMBP2 gene in spinal muscular atrophy with respiratory distress type 1.2005
- Author(s)
  Tachi N, Kikuchi S, Kozuka N, et al.
- Journal Title
  
  Pediatr Neurol 32
  
  Pages: 288-290
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] ホルマリン固定組織からのDNA抽出法とPCR法による遺伝子解析.2005
- Author(s)
  菊池真, 舘延忠, 小塚直樹他
- Journal Title
  
  札幌医誌 74
  
  Pages: 39-44
- NAID
  110001456517
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] Study of correlation between CTG repeat lengths and muscle power in myotonic dystrophy patients2005
- Author(s)
  Kikuchi S, Tachi N, Kozuka N et al.
- Journal Title
  
  Sougou Rhiha 33
  
  Pages: 167-173
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] A new mutation of IGHMBP2 In spinal muscular atrophy with respiratory disgtress2005
- Author(s)
  Tachi N, Kikuchi S, Kozuka N, Nogami A.
- Journal Title
  
  Pediatr Neural 32
  
  Pages: 288-290
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] A new mutation of IGHMBP2 gene in spinal muscular atrophy with2005
- Author(s)
  Tachi N, Kikuchi S, Kozuka N
- Journal Title
  
  Pediatr Neurol 32
  
  Pages: 288-290
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] Structural analysis of leucine-rich-repeat bvariants in proteins associated with human diseases.2005
- Author(s)
  Matsushima N, Tachi N et al.
- Journal Title
  
  Cell Mol Life Sci 62
  
  Pages: 2771-2791
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] A new mutation of IGHMBP2 gene in spinal muscular atrophy type 1.2005
- Author(s)
  Tachi N, Kikuchi S et al.
- Journal Title
  
  Pediatr Neurol 32
  
  Pages: 288-290
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] 1) Aprataxin変異遺伝子689insT患者の小脳症状、末梢神経症状に関する報告.2005
- Author(s)
  堀本佳誉, 舘延忠, 小塚直樹他
- Journal Title
  
  北海道理学療法 22
  
  Pages: 58-62
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] Aprataxin変異遺伝子689insT患者の小脳症状、末梢神経症状に関する報告.2005
- Author(s)
  堀本佳誉, 舘延忠, 小塚直樹他
- Journal Title
  
  北海道理学療法 22
  
  Pages: 58-62
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] 筋緊張性ジストロフィー3塩基反復配列(CTG repeat)と数と筋力との関係2005
- Author(s)
  菊池真, 舘延忠, 小塚直樹他
- Journal Title
  
  総合リハ 33
  
  Pages: 167-173
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] Structural analysis of leucine-rich-repeat bvariants in proteins associated with human diseases.2005
- Author(s)
  Matsusima N, Tachi N, Kuroki Y, et al.
- Journal Title
  
  Cell Mol Life Sci 62
  
  Pages: 2771-2791
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] A new mutation of IGHMBP2 gene in spinal muscular atrophy with2005
- Author(s)
  Tachi N, Kikuchi S, Kozuka N, et al.
- Journal Title
  
  Pediatr Neurol 32
  
  Pages: 288-290
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] 先天性筋強直性ジストロフィー症における3塩基反復配列(CTGリピート)数と筋組織所見の関係.2005
- Author(s)
  菊池真, 舘延忠, 小塚直樹他
- Journal Title
  
  総合リハ 33
  
  Pages: 167-173
- NAID
  40006627637
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591100
[Journal Article] 父親由来将に筋緊張性ジストロフィー症における研究2003
- Author(s)
  菊池真, 舘延忠, 小塚直樹他
- Journal Title
  
  札幌医科大学保健医療学部紀要 6
  
  Pages: 43-48
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] Analysis of CTG repeat in Myotonic dystrophy using Non-RI southern2003
- Author(s)
  Kozuka N, Tachi N, Kikuchi S et al.
- Journal Title
  
  Nou to Hatatsu 35
  
  Pages: 380-387
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] 筋緊張性ジストロフィー症CTGリピートのNon-RIサザン法による解析2003
- Author(s)
  小塚直樹, 舘延忠, 菊池真他
- Journal Title
  
  脳と発達 35
  
  Pages: 380-387
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] 筋緊張性ジストロフィーCTG repeatのNon-RIサザン法による解析2003
- Author(s)
  小塚直樹, 舘延忠, 菊池真, 他
- Journal Title
  
  脳と発達 35
  
  Pages: 380-387
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] Study of myotonic dystrophy inherited from fathers2003
- Author(s)
  Kikuchi S, Tachi N, Kozuka N et al.
- Journal Title
  
  School of Healt Sciences, Sapporo University Kiyou 6
  
  Pages: 43-48
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] 父親由来の筋緊張性ジストロフィーにおける研究2003
- Author(s)
  菊池真, 舘延忠, 小塚直樹他
- Journal Title
  
  札幌医科大学保健医療学部紀要 6
  
  Pages: 43-48
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] 「特異な脳炎脳症後てんかん一群」と考えられた1女児例2003
- Author(s)
  鈴木将史, 舘延忠, 桜井のどか他
- Journal Title
  
  臨小医 51
  
  Pages: 115-120
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] A female case of specific epilepsy after encephalitis2003
- Author(s)
  Suzuki S, Tachi N, Sakurai N et al.
- Journal Title
  
  Rinsyou Syouni Igaku 51
  
  Pages: 115-120
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Journal Article] 「特異な脳症後てんかんの一群」と考えられた1女児例2003
- Author(s)
  鈴木将史, 舘延忠, 桜井のどか他
- Journal Title
  
  臨小医 51
  
  Pages: 115-120
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591119
[Presentation] 脊髄性筋委縮症のSMN転写産物の検討2013
- Author(s)
  舘　延忠
- Organizer
  ２１回日本小児神経学会北海道地方会
- Place of Presentation
  札幌市
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] 脊髄性筋委縮症の SMN転写産物の検討2013
- Author(s)
  舘延忠
- Organizer
  第21回日本小児神経学会北街道地方会
- Place of Presentation
  札幌
- Year and Date
  2013-03-23
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] 家族性片頭痛の1家系2013
- Author(s)
  二階堂弘輝, 舘延忠
- Organizer
  第21回日本小児神経学会北街道地方会
- Place of Presentation
  札幌
- Year and Date
  2013-03-23
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] Marinesco-Sjogren症候群の 22歳女児の1剖検例ー心筋の微細構造を中心にー2012
- Author(s)
  二階堂弘輝, 舘延忠
- Organizer
  第54回日本小児神経学会
- Place of Presentation
  札幌
- Year and Date
  2012-05-12
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] 小児期発症のジスとニア:Dopa-rersponsive dystonia (Segawa 病)を中心に2012
- Author(s)
  舘延忠
- Organizer
  第20回日本小児神経学会北海道地方会
- Place of Presentation
  札幌
- Year and Date
  2012-11-17
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] 新しいGCH1遺伝子変異を持つDopa-responsive dystoniaの一卵性３つ子を含む１家系2012
- Author(s)
  舘　延忠
- Organizer
  第54回日本小児神経学会総会
- Place of Presentation
  札幌市
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] 新しいGCH1遺伝子を持つDopa-responsive dystoniaの一卵性3つ子を含む一家系2012
- Author(s)
  舘延忠
- Organizer
  第54回日本小児神経学会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] Myotubular myopathyの遺伝子診断2011
- Author(s)
  舘延忠、内田英二, ら
- Organizer
  第53回日本小児神経学会総会
- Place of Presentation
  横浜
- Year and Date
  2011-05-22
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] Myotubular myopathyの遺伝子診断2011
- Author(s)
  舘延忠
- Organizer
  第53回日本小児神経学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] 瀬川病の1家系2010
- Author(s)
  大屋一博、舘延忠、二階堂弘輝, ら
- Organizer
  第52回日本小児神経学会総会
- Place of Presentation
  福岡
- Year and Date
  2010-05-21
- Data Source
  KAKENHI-PROJECT-22591133
[Presentation] 周期性失調症2型の1 家系2010
- Author(s)
  二階堂弘輝, 舘延忠
- Organizer
  第52回日本小児神経学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-22591133

1. YAMASITA Tosiharu (50167706)

# of Collaborated Projects: 6 results

# of Collaborated Products: 0 results
2. KOZUKA Naoki (90225459)

# of Collaborated Projects: 4 results

# of Collaborated Products: 17 results
3. KIKUCHI Sin (20404585)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
4. OHYA Kazuhiro (60438067)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
5. UYEMURA Keiichi (90049792)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. TAKEDA Yasuo (60245462)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. OHNISHI Akio (50091278)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. HAYASAKA Kiyoshi (20142961)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. NINOMIYA Tahafumi (80156140)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

TACHI Nobutada 舘 延忠

館 延忠 タチ ノブタダ

舘 延忠 タチ ノブタダ

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Treatment of sodium valproate and amantazine hydrochloride in spinal muscular atrophyPrincipal Investigator

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Analysis of peripheral neuropathy in rat cultured nerve introduced mutant IGHMBP2 cDNA.Principal Investigator

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Establishment of complementation group diagnosis of xeroderma pigmentosum by using adenovirus vector

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Axonal degeneration of rat culured nerve introduced mutant aprata in cDNAPrincipal Investigator

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Identity of hereditary cerebellar ataxia, peripheral neuropathy, and hypoalbuminemiaPrincipal Investigator

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Myelination in cultured rat peripheral nerve inducted mutant Po c DNA.Principal Investigator

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Molecular and patho-physiological atudies on hereditary neuropathy.

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DNA diagnosis of congenital myotonic dystrophyPrincipal Investigator

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[Journal Article] ラモトリギンの長期使用例の経験2012

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[Journal Article] A myotonic dystrophy 1 patient complicated with placental adherence after miscarriage of one dichorionic diamniotic twin following her tenth in vitro fertilization and embryotransfer2012

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[Journal Article] A new mutation of GCH1 in triplets family with dopa-responsive dystonia2011

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[Journal Article] A new mutation of GCH1 in triplets family with dopa-responsive dystonia2011

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[Journal Article] Aprataxin遺伝子変異(689insT)が培養ラツト後根神経節の髄鞘形成に及ぼす影響について2011

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[Journal Article] Aprataxin遺伝子変異(689insT)が培養ラツト後根神経節の髄鞘形成に及ぼす影響について2011

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[Journal Article] 髄鞘形成期おける初代培養ラツト後根神経節細胞への組み換えアデノウイルスを用いた変異MPZ cDNAの導入2011

Author(s)

TACHI Nobutada 舘延忠

館延忠タチノブタダ

舘延忠タチノブタダ