Defective fast inactivation recovery of Nav1.4 in congenital myasthenic syndrome-Reference-Cited by-同舟云学术

Defective fast inactivation recovery of Nav1.4 in congenital myasthenic syndrome

Published:2015-03-27 Issue:5 Volume:77 Page:840-850
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Arnold W. David¹^ORCID,Feldman Daniel H.²,Ramirez Sandra²³,He Liuyuan²⁴,Kassar Darine¹,Quick Adam¹,Klassen Tara L.⁵,Lara Marian²,Nguyen Joanna²,Kissel John T.¹,Lossin Christoph²,Maselli Ricardo A.²

Affiliation:

1. Department of Neurology; Ohio State University Wexner Medical Center; Columbus OH

2. Department of Neurology; University of California; Davis Sacramento CA

3. Sacramento State University; Sacramento CA

4. Drexel University; Philadelphia PA

5. Faculty of Pharmaceutical Sciences; University of British Columbia; Vancouver British Columbia Canada

Funder

NIH National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.24389/fullpdf

Reference50 articles.

1. Current status of the congenital myasthenic syndromes;Engel;Neuromuscul Disord,2012

2. Synaptic dysfunction in congenital myasthenic syndromes;Beeson;Ann N Y Acad Sci,2012

3. What have we learned from the congenital myasthenic syndromes;Engel;J Mol Neurosci,2010

4. Structural factors influencing the efficacy of neuromuscular transmission;Slater;Ann N Y Acad Sci,2008

5. End-plate voltage-gated sodium channels are lost in clinical and experimental myasthenia gravis;Ruff;Ann Neurol,1998

Cited by 51 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

2. A retrospective study of accuracy and usefulness of electrophysiological exercise tests;Journal of Neurology;2023-12-06

3. Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes—A Comprehensive Review;International Journal of Molecular Sciences;2023-02-13

4. Clinical comparison and functional study of the L703P: a recurrent mutation in human SCN4A that causes sodium channel myotonia;Neuromuscular Disorders;2022-10

5. Case report: Novel SCN4A variant associated with a severe congenital myasthenic syndrome/myopathy phenotype;Frontiers in Pediatrics;2022-08-26