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769 results

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Page 1
Absence of sarcoplasmic myxovirus resistance protein A (MxA) expression in antisynthetase syndrome in a cohort of 194 cases.
Inoue M, Tanboon J, Okubo M, Theerawat K, Saito Y, Ogasawara M, Indrawati LA, Uruha A, Okiyama N, Fujimoto M, Suzuki S, Nishino I. Inoue M, et al. Among authors: nishino i. Neuropathol Appl Neurobiol. 2019 Aug;45(5):523-524. doi: 10.1111/nan.12551. Epub 2019 May 29. Neuropathol Appl Neurobiol. 2019. PMID: 30959571 No abstract available.
Diagnostic potential of sarcoplasmic myxovirus resistance protein A expression in subsets of dermatomyositis.
Uruha A, Allenbach Y, Charuel JL, Musset L, Aussy A, Boyer O, Mariampillai K, Landon-Cardinal O, Rasmussen C, Bolko L, Maisonobe T, Leonard-Louis S, Suzuki S, Nishino I, Stenzel W, Benveniste O. Uruha A, et al. Among authors: nishino i. Neuropathol Appl Neurobiol. 2019 Aug;45(5):513-522. doi: 10.1111/nan.12519. Epub 2018 Nov 22. Neuropathol Appl Neurobiol. 2019. PMID: 30267437
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
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.
Sweat retention anhidrosis associated with tubular aggregate myopathy.
Ishitsuka Y, Inoue S, Furuta J, Koguchi-Yoshioka H, Nakamura Y, Watanabe R, Okiyama N, Fujisawa Y, Enokizono T, Fukushima H, Suzuki H, Nishino I, Kosaki K, Fujimoto M. Ishitsuka Y, et al. Among authors: nishino i. Br J Dermatol. 2019 Nov;181(5):1104-1106. doi: 10.1111/bjd.18175. Epub 2019 Aug 21. Br J Dermatol. 2019. PMID: 31145807 No abstract available.
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
[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.
769 results