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Acta Neurologica Scandinavica|March 23, 2007
Psychiatric disorders appear equally in patients with myotonic dystrophy, facioscapulohumeral dystrophy, and hereditary motor and sensory neuropathy type IJ S Kalkman, M L Schillings, M J Zwarts, et al.Disability and Rehabilitation|October 31, 2025
Health-related quality of life, pain, and fatigue in myotonic dystrophy type 2: a 13-year follow-up studyM J Damen, K Mul, B G M van Engelen, et al.American Journal of Physical Medicine & Rehabilitation|May 1, 2009
Sensory nerve conduction studies in neuralgic amyotrophyNens van Alfen, Willem J Huisman, S Overeem, et al.Journal of Muscle Research and Cell Motility|October 5, 2002
Calcium regulation and muscle diseaseI M P Gommans, M H M Vlak, A de Haan, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 30, 2009
Strong association between myotonic dystrophy type 2 and autoimmune diseasesA A Tieleman, A A den Broeder, A-E van de Logt, et al.Neuromuscular Disorders : NMD|June 23, 2009
Muscle ultrasound measurements and functional muscle parameters in non-dystrophic myotonias suggest structural muscle changesJ Trip, S Pillen, C G Faber, et al.Journal of Neurology|March 3, 2009
Health status in non-dystrophic myotonias: close relation with pain and fatigueJ Trip, J de Vries, G Drost, et al.Nederlands Tijdschrift Voor Tandheelkunde|February 26, 2010
[Facioscapulohumeral muscular dystrophy]J Wilbers, R R Frants, B G M van Engelen, et al.Neurology|January 26, 2005
The lethal phenotype of a homozygous nonsense mutation in the lamin A/C geneB G M van Engelen, A Muchir, C J Hutchison, et al.Neuromuscular Disorders : NMD|November 15, 2023
Establishing the role of muscle ultrasound as an imaging biomarker in facioscapulohumeral muscular dystrophyS C C Vincenten, S Teeselink, N C Voermans, et al.Pageof 9