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Pure cerebellar ataxia phenotype in Machado-Joseph disease.
Ishikawa K, Mizusawa H, Igarashi S, Takiyama Y, Tanaka H, Ohkoshi N, Shoji S, Tsuji S. Ishikawa K, et al. Among authors: ohkoshi n. Neurology. 1996 Jun;46(6):1776-7. doi: 10.1212/wnl.46.6.1776. Neurology. 1996. PMID: 8649595 No abstract available.
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.
Ishikawa K, Tanaka H, Saito M, Ohkoshi N, Fujita T, Yoshizawa K, Ikeuchi T, Watanabe M, Hayashi A, Takiyama Y, Nishizawa M, Nakano I, Matsubayashi K, Miwa M, Shoji S, Kanazawa I, Tsuji S, Mizusawa H. Ishikawa K, et al. Among authors: ohkoshi n. Am J Hum Genet. 1997 Aug;61(2):336-46. doi: 10.1086/514867. Am J Hum Genet. 1997. PMID: 9311738 Free PMC article.
Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells.
Ishikawa K, Owada K, Ishida K, Fujigasaki H, Shun Li M, Tsunemi T, Ohkoshi N, Toru S, Mizutani T, Hayashi M, Arai N, Hasegawa K, Kawanami T, Kato T, Makifuchi T, Shoji S, Tanabe T, Mizusawa H. Ishikawa K, et al. Among authors: ohkoshi n. Neurology. 2001 Jun 26;56(12):1753-6. doi: 10.1212/wnl.56.12.1753. Neurology. 2001. PMID: 11425948
137 results