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2015-11-27

学会発表

[特別講演、シンポジウム]
西野一三: 筋ジストロフィーの新規治療法. 第33回日本神経治療学会総会, 名古屋, 11.27, 2015

2015-11-14

学会発表

[特別講演、シンポジウム]
Noguchi S: Sialic acid therapy in GNE myopathy: Lessons from other HIBMs. 215th ENMC International Workshop, Amsterdam, The Netherlands, 11.14, 2015

2015-11-13

学会発表

[特別講演、シンポジウム]
Noguchi S: Clinical and molecular aspects: Asian cohort. 215th ENMC International Workshop, Amsterdam, The Netherlands, 11.13, 2015

2015-10-24

学会発表

[特別講演、シンポジウム]
西野一三: 筋型糖原病の診断と治療~ポンペ病を中心に~. 第2回筋ジストロフィー医療研究会, 大阪, 10.24, 2015

2015-10-05

学会発表

[国際学会]
Hamanaka K, Goto K, Arai M, Nagao K, Obuse C, Noguchi S, Hayashi YK, Mitsuhashi S, Nishino I: SMCHD1 haploinsufficiency: common in Japan? FSH Society Facioscapulohumeral Muscular Dystrophy [FSHD] 2015 International Research Consortium & Research Planning Meetings, Boston, US, 10.5, 2015

2015-10-02

学会発表

[国際学会]
Uruha A, Noguchi S, Sato W, Nishimura H, Mitsuhashi S, Yamamura T, Nishino I: Plasma IP-10 level distinguishes inflammatory myopathy. 20th International Congress of the World Muscle Society, Brighton, UK, 10.2, 2015

2015-10-02

学会発表

[国際学会]
Kohashi K, Ishiyama A, Takeshita E, Shimizu-Motohashi Y, Saito T, Nakagawa E, Komaki H, Sugai K, Nishino I, Saito W, Takaso M, Sasaki M: Early scoliosis surgery may prevent deterioration of respiratory function of in Ullrich congenital muscular dystrophy. 20th International Congress of the World Muscle Society, Brighton, UK, 10.2, 2015

2015-10-02

学会発表

[国際学会]
Tanboon J, Noguchi S, Mitsuhashi S, Nishino I: Homozygous splicing mutation in ISPD gene in a girl with Walker-Warburg syndrome. 20th International Congress of the World Muscle Society, Brighton, UK, 10.2, 2015

2015-10-02

学会発表

[国際学会]
Noguchi S, Dong M, Endo Y, Hayashi YK, Yoshida S, Nonaka I, Nishino I: DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of α-dystroglycan. 20th International Congress of the World Muscle Society, Brighton, UK, 10.2, 2015

2015-10-02

学会発表

[国際学会]
Endo Y, Dong M, Noguchi S, Ogawa M, Hayashi YK, Kuru S, Sugiyama K, Nagai S, Ozasa S, Nonaka I, Nishino I: Milder phenotype of muscular dystrophy due to POMGNT2 mutations. 20th International Congress of the World Muscle Society, Brighton, UK, 10.2, 2015

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