2015-05-22

学会発表

[一般学会]
Uruha A, Noguchi S, Mitsuhashi S, Sato W, Yamamura T, Nishimura H, Nishino I: Plasma IP-10 level distinguishes inflammatory myopathy. 第56回日本神経学会学術大会, 新潟, 5.22,2015

2015-05-20

学会発表

[一般学会]
西川敦子, 西野一三: 皮膚筋炎の筋病理診断におけるMxA染色の有用性. 第56回日本神経学会学術大会, 新潟, 5.20,2015

2015-05-06

原著

森まどか,西野一三:シアル酸補充療法-GNEミオパチー(縁取り空胞を伴う遠位型ミオパチー)治療への試み.Brain Nerve. 67(9): 1115-1123, Sep, 2015

2015-05-05

原著

Ogawa S, Hattori K, Sasayama D, Yokota Y, Matsumura R, Matsuo J, Ota M, Hori H, Teraishi T, Yoshida S, Noda T, Ohashi Y, Sato H, Higuchi T, Motohashi N, Kunugi H.
Reduced cerebrospinal fluid ethanolamine concentration in major depressive disorder.
Sci Rep. 2015 Jan 15;5:7796.

2015-05-04

原著

Dong M, Noguchi S, Endo Y, Hayashi YK, Yoshida S, Nonaka I, Nishino I.
DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of α-dystroglycan.
Neurology. 2015 Jan 20;84(3):273-279.

2015-05-03

原著

Watanabe Y, Suzuki S, Nishimura H, Murata KY, Kurashige T, Ikawa M, Asahi M, Konishi H, Mitsuma S, Kawabata S, Suzuki N, Nishino I.
Statins and myotoxic effects associated with anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase autoantibodies: an observational study in Japan.
Medicine (Baltimore). 2015 Jan;94(4):e416.

2015-05-02

原著

Wang CH, Liang WC, Minami N, Nishino I, Jong YJ.
Limb-girdle Muscular Dystrophy Type 2A with Mutation in CAPN3: The First Report in Taiwan
Pediatr Neonatol. 2015 Feb;56(1):62-5.

2015-05-01

原著

Sakai C, Yamaguchi S, Sasaki M, Miyamoto Y, Matsushima Y, Goto Y.
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.
Hum Mutat. 2015 Feb;36(2):232-9.

2015-04-30

原著

Kawase K, Nishino I, Sugimoto M, Kouwaki M, Koyama N, Yokochi K.
Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event.
Brain Dev. 2015 Feb;37(2):265-269.

2015-04-29

原著

Tanboon J, Hayashi YK, Nishino I, Sangruchi T.
Kyphoscoliosis and easy fatigability in a 14-year-old boy.
Neuropathology. 2015 Feb;35(1):91-93.