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Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype.
Takahashi T, Aoki M, Tateyama M, Kondo E, Mizuno T, Onodera Y, Takano R, Kawai H, Kamakura K, Mochizuki H, Shizuka-Ikeda M, Nakagawa M, Yoshida Y, Akanuma J, Hoshino K, Saito H, Nishizawa M, Kato S, Saito K, Miyachi T, Yamashita H, Kawai M, Matsumura T, Kuzuhara S, Ibi T, Sahashi K, Nakai H, Kohnosu T, Nonaka I, Arahata K, Brown RH Jr, Saito H, Itoyama Y. Takahashi T, et al. Among authors: saito k, saito h. Neurology. 2003 Jun 10;60(11):1799-804. doi: 10.1212/01.wnl.0000068333.43005.12. Neurology. 2003. PMID: 12796534
A case of dysferlinopathy presenting choreic movements.
Takahashi T, Aoki M, Imai T, Yoshioka M, Konno H, Higano S, Onodera Y, Saito H, Kimura I, Itoyama Y. Takahashi T, et al. Among authors: saito h. Mov Disord. 2006 Sep;21(9):1513-5. doi: 10.1002/mds.21027. Mov Disord. 2006. PMID: 16817213
Characteristics of the increase in plasma brain natriuretic peptide level in left ventricular systolic dysfunction, associated with muscular dystrophy in comparison with idiopathic dilated cardiomyopathy.
Demachi J, Kagaya Y, Watanabe J, Sakuma M, Ikeda J, Kakuta Y, Motoyoshi I, Kohnosu T, Sakuma H, Shimazaki S, Sakai H, Kimpara T, Takahashi T, Omura K, Okada M, Saito H, Shirato K. Demachi J, et al. Among authors: saito h. Neuromuscul Disord. 2004 Nov;14(11):732-9. doi: 10.1016/j.nmd.2004.08.002. Neuromuscul Disord. 2004. PMID: 15482958
8,506 results