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Page 1
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.
Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M, Aoki M, Nonaka I. Nishino I, et al. Among authors: kawai m. Neurology. 2002 Dec 10;59(11):1689-93. doi: 10.1212/01.wnl.0000041631.28557.c6. Neurology. 2002. PMID: 12473753
A new diagnostic test for VLCAD deficiency using immunohistochemistry.
Ohashi Y, Hasegawa Y, Murayama K, Ogawa M, Hasegawa T, Kawai M, Sakata N, Yoshida K, Yarita H, Imai K, Kumagai I, Murakami K, Hasegawa H, Noguchi S, Nonaka I, Yamaguchi S, Nishino I. Ohashi Y, et al. Among authors: kawai m. Neurology. 2004 Jun 22;62(12):2209-13. doi: 10.1212/01.wnl.0000130486.54839.15. Neurology. 2004. PMID: 15210884
Distal myopathy with rimmed vacuoles.
Nonaka I, Murakami N, Suzuki Y, Kawai M. Nonaka I, et al. Among authors: kawai m. Neuromuscul Disord. 1998 Jun;8(5):333-7. doi: 10.1016/s0960-8966(98)00027-3. Neuromuscul Disord. 1998. PMID: 9673988 Clinical Trial.
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: kawai h, kawai m. Neurology. 2003 Jun 10;60(11):1799-804. doi: 10.1212/01.wnl.0000068333.43005.12. Neurology. 2003. PMID: 12796534
Nebulin is normally expressed in nemaline myopathy.
Imoto C, Kimura S, Kawai M, Nonaka I. Imoto C, et al. Among authors: kawai m. Acta Neuropathol. 1999 May;97(5):433-6. doi: 10.1007/s004010051011. Acta Neuropathol. 1999. PMID: 10334479
2,419 results