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Journal of Neuromuscular Diseases|July 12, 2021
Clinical Outcome Evaluations and CBT Response Prediction in Myotonic DystrophyDaniël van As, Kees Okkersen, Guillaume Bassez, et al.BMC Neurology|April 28, 2015
Effectiveness and cost-effectiveness of a self-management group program to improve social participation in patients with neuromuscular disease and chronic fatigue: protocol of the Energetic studyYvonne Veenhuizen, Edith H C Cup, Jan T Groothuis, et al.Neurorehabilitation and Neural Repair|December 28, 2022
Cerebral Adaptation Associated with Peripheral Nerve Recovery in Neuralgic Amyotrophy: A Randomized Controlled TrialRenee Lustenhouwer, Ian G M Cameron, Nens van Alfen, et al.Pathogens (Basel, Switzerland)|June 24, 2022
Monitoring and Surveillance of Small Ruminant Health in The NetherlandsEveline Dijkstra, Piet Vellema, Karianne Peterson, et al.Neurology|May 24, 2019
Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRILinda Heskamp, Marlies van Nimwegen, Marieke J Ploegmakers, et al.Human Molecular Genetics|November 17, 2018
Single-cell RNA sequencing in facioscapulohumeral muscular dystrophy disease etiology and developmentAnita van den Heuvel, Ahmed Mahfouz, Susan L Kloet, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2005
Histology of hereditary neuralgic amyotrophyN van Alfen, A A W M Gabreëls-Festen, H J Ter Laak, et al.Brain : a Journal of Neurology|April 25, 2000
Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosisA Verrips, L H Hoefsloot, G C Steenbergen, et al.Journal of Neurology|June 4, 2018
Fatigue, not self-rated motor symptom severity, affects quality of life in functional motor disordersJ M Gelauff, E M Kingma, J S Kalkman, et al.Disability and Rehabilitation|September 14, 2007
Development of a tool to guide referral of patients with neuromuscular disorders to allied health services. Part oneAllan J Pieterse, Edith H C Cup, Simone Knuijt, et al.Pageof 84