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Neuromuscular Disorders : NMD|July 19, 2003
Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contracturesA T J M Helderman-van den Enden, H B Ginjaar, A L J Kneppers, et al.Clinical Radiology|December 15, 2010
Interobserver agreement on MRI evaluation of patients with cervical radiculopathyB Kuijper, A Beelen, B F van der Kallen, et al.Neuromuscular Disorders : NMD|January 22, 2002
Two amino-acid substitutions in the myelin protein zero gene of a case of Charcot-Marie-Tooth disease associated with light-near dissociationH M E Bienfait, F Baas, A A W M Gabreëls-Festen, et al.European Journal of Neurology|August 2, 2006
EFNS guideline on diagnosis and management of post-polio syndrome. Report of an EFNS task forceE Farbu, N E Gilhus, M P Barnes, et al.Neuromuscular Disorders : NMD|July 23, 1998
Genetic heterogeneity in Miyoshi-type distal muscular dystrophyW H Linssen, M de Visser, N C Notermans, et al.Acta Neuropathologica|January 1, 1992
Secondary changes of the motor endplate in Lambert-Eaton myasthenic syndrome: a quantitative studyL F Hesselmans, F G Jennekens, J Kartman, et al.Viruses|September 27, 2025
Living Together Apart: Quantitative Perspectives on the Costs and Benefits of a Multipartite Genome Organization in VirusesMarcelle L Johnson, Dieke Boezen, Alexey A Grum-Grzhimaylo, et al.Heart (British Cardiac Society)|March 20, 1998
The heart in limb girdle muscular dystrophyA J van der Kooi, W G de Voogt, P G Barth, et al.Neurology|September 19, 2008
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromesF Brugman, H Scheffer, J H J Wokke, et al.Journal of Neurology|December 24, 1997
Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year periodE M Hoogerwaard, W G de Voogt, A A Wilde, et al.Pageof 25