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Cell Metabolism|September 3, 2015
Statin-Induced Myopathy Is Associated with Mitochondrial Complex III InhibitionTom J J Schirris, G Herma Renkema, Tina Ritschel, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 20, 2002
Difference in distribution of muscle weakness between myasthenia gravis and the Lambert-Eaton myasthenic syndromeP W Wirtz, M Sotodeh, M Nijnuis, et al.Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.British Journal of Clinical Pharmacology|May 1, 2021
Phase 1 clinical trial of losmapimod in facioscapulohumeral dystrophy: Safety, tolerability, pharmacokinetics, and target engagementMichelle L Mellion, Lucienne Ronco, Cecile L Berends, et al.Annals of the Rheumatic Diseases|January 13, 2001
Autoantibody profiles in the sera of European patients with myositisR Brouwer, G J Hengstman, W Vree Egberts, et al.JAMA|December 12, 2018
Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 TrialsBas C Stunnenberg, Joost Raaphorst, Hans M Groenewoud, et al.Neurology|May 16, 2007
Phenotype of Charcot-Marie-Tooth disease Type 2H M E Bienfait, F Baas, J H T M Koelman, et al.Plos Genetics|November 9, 2013
Human intellectual disability genes form conserved functional modules in DrosophilaMerel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.Neuromuscular Disorders : NMD|May 24, 2016
The epidemiology of neuromuscular disorders: Age at onset and gender in the NetherlandsJohanna C W Deenen, Pieter A van Doorn, Catharina G Faber, et al.European Journal of Human Genetics : EJHG|February 28, 2018
The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?Natalia Teixeira, Annemieke van der Hout, Jan C Oosterwijk, et al.Pageof 84