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Journal of Neurology|October 28, 2020
Characterizing the face in facioscapulohumeral muscular dystrophyT G J Loonen, C G C Horlings, S C C Vincenten, et al.Frontiers in Cardiovascular Medicine|July 16, 2025
Evaluation of echocardiography monitoring in myotonic dystrophy type 1 patientsD S H Bovenkerk, C E W Janssen, F M A Van den Heuvel, et al.Neurology|July 26, 2006
Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasiaJ A P Hiel, B G M van Engelen, C M R Weemaes, et al.Neuromuscular Disorders : NMD|April 3, 2018
Prevalence and mutation spectrum of skeletal muscle channelopathies in the NetherlandsB C Stunnenberg, J Raaphorst, J C W Deenen, 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.Neurology|May 16, 2007
Phenotype of Charcot-Marie-Tooth disease Type 2H M E Bienfait, F Baas, J H T M Koelman, et al.Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.Neurology|December 30, 2004
Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositisU A Badrising, G M Th Schreuder, M J Giphart, et al.European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.Annals of the Rheumatic Diseases|January 27, 2017
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositisJ B Lilleker, A Rietveld, S R Pye, et al.Pageof 9