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Neurology|October 26, 2005
Multidisciplinary ALS care improves quality of life in patients with ALSJ P Van den Berg, S Kalmijn, E Lindeman, et al.
Neurology|September 24, 2011
Family history of neurodegenerative and vascular diseases in ALS: a population-based studyM H B Huisman, S W de Jong, M C Verwijs, et al.
Neuromuscular Disorders : NMD|July 23, 1998
A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophyA J van der Kooi, M de Visser, M van Meegen, et al.
Brain : a Journal of Neurology|December 16, 1997
Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patientsW H Linssen, N C Notermans, Y Van der Graaf, et al.
Evolutionary Applications|January 9, 2015
Mixed infections and the competitive fitness of faster-acting genetically modified virusesMark P Zwart, Wopke Van Der Werf, Monique M Van Oers, et al.
Nucleic Acids Research|October 12, 2000
Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatographyB J van Den Bosch, R F de Coo, H R Scholte, et al.
Brain : a Journal of Neurology|April 12, 2003
Sporadic lower motor neuron disease with adult onset: classification of subtypesR M van den Berg-Vos, J Visser, H Franssen, et al.
Journal of the Neurological Sciences|March 23, 2025
Awareness of bone strength in patients with neuromuscular disorders: ERN EURO-NMD clinician survey and European patient surveyM T A Kruse, B A S Olde Dubbelink, M Kroneman, et al.
Neurology|June 12, 2002
Mimic syndromes in sporadic cases of progressive spinal muscular atrophyJ Visser, R M van den Berg-Vos, H Franssen, et al.
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