Papers - TAKASHIMA Hiroshi
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Nakagawa M, Suehara M, Saito A, Takashima H, Umehara F, Saito M, Kanzato N, Matsuzaki T, Takenaga S, Sakoda S, Izumo S, Osame M . A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths . Neurology52 1271 - 1275 1999.1Reviewed
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Takashima H, Nakagawa M, Suehara M, Saito M, Saito A, Kanzato N, Matuzaki T, Hirata K, Terwilliger JD, Osame M . Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1. . Neuromuscul Disord9 232 - 238 1999.1Reviewed
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Takashima H, Nakagawa M, Nakahara K, Suehara M, Matsuzaki T, Higuchi I, Higa H, Arimura K, Iwamasa T, Izumo S, Osame M. . A New Type of Hereditary Motor and Sensory Neuropathy linked to chromosome 3. . Annals of Neurology41 ( 6 ) 771 - 780 1997.3Reviewed
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Hiroshi Takashima , Nakagawa M, Nakahara K, Suehara M, Matsuzaki T, Higuchi I, Higa H, Arimura K, Iwamasa T, Izumo S, Osame M . A new type of Hereditary motor and sensory neuropathy linked to chromosome 3 . Ann Neurol 41 771 - 780 1997.1Reviewed
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Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, Salih MAM, Takashima H, Boerkoel CF . Spinocerebellar Ataxia with Axonal Neuropathy Type 1. . 1993