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771 results

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Page 1
Beevor's sign: a potential clinical marker for GNE myopathy.
Preethish-Kumar V, Pogoryelova O, Polavarapu K, Gayathri N, Seena V, Hudson J, Nishino I, Prasad C, Lochmüller H, Nalini A. Preethish-Kumar V, et al. Among authors: nishino i. Eur J Neurol. 2016 Aug;23(8):e46-8. doi: 10.1111/ene.13041. Eur J Neurol. 2016. PMID: 27431025 No abstract available.
GNE myopathy in India.
Nalini A, Gayathri N, Nishino I, Hayashi YK. Nalini A, et al. Among authors: nishino i. Neurol India. 2013 Jul-Aug;61(4):371-4. doi: 10.4103/0028-3886.117609. Neurol India. 2013. PMID: 24005727 Free article.
Characterization of the Asian myopathy patients with VCP mutations.
Shi Z, Hayashi YK, Mitsuhashi S, Goto K, Kaneda D, Choi YC, Toyoda C, Hieda S, Kamiyama T, Sato H, Wada M, Noguchi S, Nonaka I, Nishino I. Shi Z, et al. Among authors: nishino i. Eur J Neurol. 2012 Mar;19(3):501-9. doi: 10.1111/j.1468-1331.2011.03575.x. Epub 2011 Oct 31. Eur J Neurol. 2012. PMID: 22040362
Novel FHL1 mutations in fatal and benign reducing body myopathy.
Shalaby S, Hayashi YK, Nonaka I, Noguchi S, Nishino I. Shalaby S, et al. Among authors: nishino i. Neurology. 2009 Jan 27;72(4):375-6. doi: 10.1212/01.wnl.0000341311.84347.a0. Neurology. 2009. PMID: 19171836 No abstract available.
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.
Cortese A, Laurà M, Casali C, Nishino I, Hayashi YK, Magri S, Taroni F, Stuani C, Saveri P, Moggio M, Ripolone M, Prelle A, Pisciotta C, Sagnelli A, Pichiecchio A, Reilly MM, Buratti E, Pareyson D. Cortese A, et al. Among authors: nishino i. Eur J Neurol. 2018 Jan;25(1):154-163. doi: 10.1111/ene.13478. Epub 2017 Dec 2. Eur J Neurol. 2018. PMID: 29029362
A new congenital form of X-linked autophagic vacuolar myopathy.
Yan C, Tanaka M, Sugie K, Nobutoki T, Woo M, Murase N, Higuchi Y, Noguchi S, Nonaka I, Hayashi YK, Nishino I. Yan C, et al. Among authors: nishino i. Neurology. 2005 Oct 11;65(7):1132-4. doi: 10.1212/01.wnl.0000178979.19887.f5. Neurology. 2005. PMID: 16217076
Gene expression analyses in X-linked myotubular myopathy.
Noguchi S, Fujita M, Murayama K, Kurokawa R, Nishino I. Noguchi S, et al. Among authors: nishino i. Neurology. 2005 Sep 13;65(5):732-7. doi: 10.1212/01.wnl.0000174625.67484.4d. Neurology. 2005. PMID: 16157907
771 results