School personnel information

写真b

TAKAHASHI Masanori


URL

http://sahswww.med.osaka-u.ac.jp/~neurolog/

Gender

Male

Organization 【 display / non-display

  • 2002.12.01 - 2007.03.31, Graduate School of Medicine, Research Assistant

  • 2007.04.01 - 2014.07.31, Graduate School of Medicine, Assistant Professor

  • 2014.08.01 - 2016.03.31, Graduate School of Medicine, Associate Professor

  • 2016.04.01 - , Division of Health Sciences, Graduate School of Medicine, Professor

  • 2016.04.01 - , Osaka University Hospital

Education 【 display / non-display

Osaka University Faculty of Medicine  Graduated 1989.03
Osaka University Graduate School, Division of Medical Sciences  Completed 1994.03

Research topics 【 display / non-display

  • Na channel
    Neuroscience-general-related, Physiology-related

  • Skeletal muscle disease
    Neurology-related

Academic Society Membership 【 display / non-display

  • World Muscle Society

  • Biophysical Society

 

Academic Papers 【 display / non-display

  • A slipped-CAG DNA-binding small molecule induces trinucleotide-repeat contractions in vivo, Nakamori M, Panigrahi GB, Lanni S, Gall-Duncan T, Hayakawa H, Tanaka H, Luo J, Otabe T, Li J, Sakata A, Caron MC, Joshi N, Prasolava T, Chiang K, Masson JY, Wold MS, Wang X, Lee MYWT, Huddleston J, Munson KM, Davidson S, Layeghifard M, Edward LM, Gallon R, Santibanez-Koref M, Murata A, Takahashi MP, Eichler EE, Shlien A, Nakatani K, Mochizuki H, Pearson CE, Nat Genet, 2020.02, Papers

  • The myotonic dystrophy health index: Japanese adaption and validity testing., Mori I, Fujino H, Matsumura T, Takada H, Ogata K, Nakamori M, Innami K, Shingaki H, Imura O, Takahashi MP, Heatwole C, Muscle & nerve,59(5) 577-582, 2019.05, Papers

  • A family with both X-linked dominant Charcot-Marie-Tooth disease and myotonic dystrophy type 1 mutations with phenotypic variations, Mori Chiaki, Nakatani Rie, Nakamori Masayuki, Matsumura Tsuyoshi, Takahashi Masanori P., Fujimura Harutoshi, Mochizuki Hideki, Sakoda Saburo, NEUROLOGY AND CLINICAL NEUROSCIENCE,7(2) 88-90, 2019.03, Papers

  • Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease., Wood L, Bassez G, Bleyenheuft C, Campbell C, Cossette L, Jimenez-Moreno AC, Dai Y, Dawkins H, Manera JAD, Dogan C, El Sherif R, Fossati B, Graham C, Hilbert J, Kastreva K, Kimura E, Korngut L, Kostera-Pruszczyk A, Lindberg C, Lindvall B, Luebbe E, Lusakowska A, Mazanec R, Meola G, Orlando L, Takahashi MP, Peric S, Puymirat J, Rakocevic-Stojanovic V, Rodrigues M, Roxburgh R, Schoser B, Segovia S, Shatillo A, Thiele S, Tournev I, van Engelen B, Vohanka S, Lochmüller H, Orphanet journal of rare diseases,13(1) 155, 2018.09, Papers

  • Cognitive impairment and quality of life in patients with myotonic dystrophy type 1., Fujino H, Shingaki H, Suwazono S, Ueda Y, Wada C, Nakayama T, Takahashi MP, Imura O, Matsumura T, Muscle & nerve,57(5) 742-748, 2018.05, Papers

display all >>