Xin-Ming Shen

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 13

Top Topics

Bioinformatics Analysis

Muscular Dystrophy

Top Venues

International journal of molecular sciences

Annals of clinical and translational neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Kinji Ohno, Bisei Ohkawara, Xin-Ming Shen, Duygu Selcen, Andrew G Engel
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. International journal of molecular sciences 24 (4) (2023)
Kinji Ohno, Bisei Ohkawara, Xin-Ming Shen, Duygu Selcen, Andrew G Engel
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. International journal of molecular sciences 24 (4) (2023)
Kinji Ohno, Bisei Ohkawara, Xin-Ming Shen, Duygu Selcen, Andrew G Engel
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. International journal of molecular sciences 24 (4) (2023)
Zhirong Fan, Lin Lei, Shengyao Su, Shu Zhang, Nairong Xie, Ling Li, Yan Lu, Li Di, Min Wang, Min Xu, Xin-Ming Shen, Yuwei Da
Comparison between mono-tacrolimus and mono-glucocorticoid in the treatment of myasthenia gravis. Annals of clinical and translational neurology (2023)
Kinji Ohno, Bisei Ohkawara, Xin-Ming Shen, Duygu Selcen, Andrew G Engel
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. International journal of molecular sciences 24 (4) (2023)
Xin-Ming Shen, Tomohiko Nakata, Seiji Mizuno, Issei Imoto, Duygu Selcen, Kinji Ohno, Andrew G Engel
Impaired gating of γ- and ε-AChR respectively causes Escobar syndrome and fast-channel myasthenia. Annals of clinical and translational neurology (2023)
Kinji Ohno, Bisei Ohkawara, Xin-Ming Shen, Duygu Selcen, Andrew G Engel
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. International journal of molecular sciences 24 (4) (2023)
Xin-Ming Shen, Tomohiko Nakata, Seiji Mizuno, Issei Imoto, Duygu Selcen, Kinji Ohno, Andrew G Engel
Impaired gating of γ- and ε-AChR respectively causes Escobar syndrome and fast-channel myasthenia. Annals of clinical and translational neurology (2023)
Kinji Ohno, Bisei Ohkawara, Xin-Ming Shen, Duygu Selcen, Andrew G Engel
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. International journal of molecular sciences 24 (4) (2023)
Kinji Ohno, Bisei Ohkawara, Xin-Ming Shen, Duygu Selcen, Andrew G Engel
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. International journal of molecular sciences 24 (4) (2023)
Kinji Ohno, Bisei Ohkawara, Xin-Ming Shen, Duygu Selcen, Andrew G Engel
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. International journal of molecular sciences 24 (4) (2023)
Li Di, Hai Chen, Yan Lu, Duygu Selcen, Andrew G Engel, Yuwei Da, Xin-Ming Shen
Determinants of the repetitive-CMAP occurrence and therapy efficacy in slow-channel myasthenia. Neurology 95 (20) (2020)
Xin-Ming Shen, Margherita Milone, Hang-Long Wang, Brenda Banwell, Duygu Selcen, Steven M Sine, Andrew G Engel
Slow-channel myasthenia due to novel mutation in M2 domain of AChR delta subunit. Annals of clinical and translational neurology 6 (10) (2019)