Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Manami Hama"'
Autor:
Tomoya Kubota, Hidehiro Mizusawa, Yoshihiro Sugiura, Kinya Ishikawa, Masanori P. Takahashi, Yuji Takahashi, Manami Hama
Publikováno v:
Neurology and Clinical Neuroscience. 9:443-451
Autor:
Hideki Mochizuki, Shin Nabatame, Masanori P. Takahashi, Ujiakira Nishiike, Tomoya Kubota, Manami Hama, Takao Takeshima, Ruka Sato
Publikováno v:
Brain and Development. 43:952-957
Background Familial hemiplegic migraine (FHM) is an inherited autosomal dominant disorder characterized by migraine with reversible hemiplegia. FHM1 is caused by variants in CACNA1A, encoding a P/Q type neuronal voltage-gated calcium channel α subun
Autor:
Tomoya Kubota, Hiroto Takada, Tsuyoshi Matsumura, Harumasa Nakamura, Riho Horie, Masanori P. Takahashi, En Kimura, Manami Hama
Publikováno v:
Journal of the neurological sciences. 427
Myotonic dystrophy type 1 (DM1) is the most common form of muscular dystrophy in adults, affecting multiple organs, including the eyes, heart, endocrine system, and central nervous system. The broad spectrum of DM1 symptoms has been attributed to the