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686 results
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[Myopathy, hereditary with lactic acidosis].
Nishino I. Nishino I. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):247-8. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528723 Review. Japanese. No abstract available.
[X-linked myopathy with excessive autophagy].
Nishino I. Nishino I. Ryoikibetsu Shokogun Shirizu. 2001;(36):230-2. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596377 Review. Japanese. No abstract available.
Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy.
Tateyama M, Aoki M, Nishino I, Hayashi YK, Sekiguchi S, Shiga Y, Takahashi T, Onodera Y, Haginoya K, Kobayashi K, Iinuma K, Nonaka I, Arahata K, Itoyama Y. Tateyama M, et al. Among authors: nishino i. Neurology. 2002 Jan 22;58(2):323-5. doi: 10.1212/wnl.58.2.323. Neurology. 2002. PMID: 11805270
[Complex V deficiency].
Matsumoto H, Nishino I. Matsumoto H, et al. Among authors: nishino i. Nihon Rinsho. 2002 Apr;60 Suppl 4:495-8. Nihon Rinsho. 2002. PMID: 12013922 Review. Japanese. No abstract available.
686 results