舘 延忠

• 科研費等

• 舘 延忠, 須鎌 康介, 仙石 泰仁. 脊髄性筋萎縮症の診断と治療の進歩. 北海道作業療法. 2018. 35. 4. 190-200
• 舘 延忠, 高橋 悟. 小児期発症の遺伝性ジストニア Dopa-responsive Dystonia. 北海道千歳リハビリテーション大学研究紀要. 2018. 2. 9-15
• Toshiaki Endo, Tsuyoshi Baba, Asuka Sugio, Miyuki Morishita, Madoka Takahashi, Yushi Akashi, Shinichi Ishioka, Nobutada Tachi, Tomihiro Imai, Mitsuharu Tamakawa, et al. A myotonic dystrophy 1 patient complicated with placental adherence after miscarriage of one dichorionic diamniotic twin following her tenth in vitro fertilization and embryo transfer. ARCHIVES OF GYNECOLOGY AND OBSTETRICS. 2012. 286. 6. 1605-1608
• N. Tachi, S. Takahashi, M. Jo, M. Shinoda. A new mutation of GCH1 in triplets family with dopa-responsive dystonia. EUROPEAN JOURNAL OF NEUROLOGY. 2011. 18. 9. 1191-1193
• Koki Nikaido, Nobutada Tachi, Kazuhiro Ohya, Takahito Wada, Hiroyuki Tsutsumi. New mutation of CACNA1A gene in episodic ataxia type 2. PEDIATRICS INTERNATIONAL. 2011. 53. 3. 415-416

もっと見る

• A new mutation of IGHMBP2 gene in spinal muscular atrophy with respiratory distress type 1. Pediatr Neurol. 2005. 32. 288-90
• Naoki Kozuka, Nobutada Tachi, Kazuhiro Ohya, Eiji Uchida, Shin Kikuchi, Yasuhito Sengoku. Non-radioactive PCR southern method for analysis of CTG repeat in myotonic dystrophy. No To Hattatsu. 2003. 35. 5. 380-387
• Expression of peripheral myelin protein zero in sural nerve of patients with Charcot-Marie-Tooth disease 1B. Pediatr Neurol. 2001. 24. 33-5
• A double mutation in a patient with X-linked myotubular myopathy. Pediatr Neurol. 2001. 24. 297-9
• Fukuyama muscular dystrophy associated with lack of C-terminal domain of dystrophin. Pediatr Neurol. 2001. 24. 373-8

もっと見る

• - 1973 札幌医科大学
• - 1973 札幌医科大学

• 医学博士

日本小児遺伝学会 ,  日本てんかん学会 ,  日本人類遺伝学会 ,  日本神経学会 ,  日本小児神経学会 ,  日本小児科学会 ,  アジア。オセアニア小児神経学会 ,  米国人類遺伝学会 ,  Japanese Sociaty of Neurology ,  Japanese Sociaty of Child Neurology ,  Japanese Sociaty of Pediatrics