受强制性开放获取政策约束的文章 - Claudia Kay了解详情
无法在其他位置公开访问的文章：1 篇
Salbutamol therapy in congenital myasthenic syndrome due to DOK7 mutation
PJ Lorenzoni, RH Scola, CSK Kay, L Filla, APP Miranda, JMR Pinheiro, ...
Journal of the neurological sciences 331 (1-2), 155-157, 2013
强制性开放获取政策： UK Medical Research Council
可在其他位置公开访问的文章：3 篇
Molecular characterisation of congenital myasthenic syndromes in Southern Brazil
V Mihaylova, RH Scola, B Gervini, PJ Lorenzoni, CK Kay, LC Werneck, ...
Journal of Neurology, Neurosurgery & Psychiatry 81 (9), 973-977, 2010
强制性开放获取政策： German Research Foundation
Novel synaptobrevin‐1 mutation causes fatal congenital myasthenic syndrome
XM Shen, RH Scola, PJ Lorenzoni, CSK Kay, LC Werneck, J Brengman, ...
Annals of clinical and translational neurology 4 (2), 130-138, 2017
强制性开放获取政策： US National Institutes of Health
How to Spot Congenital Myasthenic Syndromes Resembling the Lambert–Eaton Myasthenic Syndrome? A Brief Review of Clinical, Electrophysiological, and Genetics Features
PJ Lorenzoni, RH Scola, CSK Kay, LC Werneck, R Horvath, H Lochmüller
NeuroMolecular Medicine 20, 205-214, 2018
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
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