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European Neurology|January 31, 2008
Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexateG J D Hengstman, J L De Bleecker, E Feist, et al.Acta Neurologica Scandinavica|April 11, 2018
Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndromeN Witting, P Laforêt, N C Voermans, et al.Journal of Neuromuscular Diseases|April 25, 2025
Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy: Data of the unite-CNM studyS Colombo, B S Cowling, L Eyler, et al.Neuromuscular Disorders : NMD|February 14, 2017
PGM1 deficiency: Substrate use during exercise and effect of treatment with galactoseN C Voermans, N Preisler, K L Madsen, et al.Molecular Metabolism|December 1, 2022
Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?M Villarreal-Salazar, A Santalla, A Real-Martínez, et al.European Journal of Neurology|May 7, 2017
European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10-year experienceA T van der Ploeg, M E Kruijshaar, A Toscano, et al.European Journal of Neurology|July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imagingG Giacomucci, M Monforte, J Diaz-Manera, et al.Acta Neuropathologica|August 30, 2019
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvementS Donkervoort, R Sabouny, P Yun, et al.Pageof 8