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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 20, 2021
Implementation of Motor Function Measure score percentile curves - Predicting motor function loss in Duchenne muscular dystrophyPatricia Hafner, Simone Schmidt, Sabine Schädelin, et al.Journal of Neurology|February 24, 2005
Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDsDirk Fischer, Maggie C Walter, Kristina Kesper, et al.Neuromuscular Disorders : NMD|April 10, 2007
Phenotypic patterns of desminopathy associated with three novel mutations in the desmin geneMontse Olivé, Judith Armstrong, Francesc Miralles, et al.Frontiers in Pharmacology|May 22, 2023
Metabolic markers of short and long-term exogenous DL-beta-hydroxybutyrate supplementation in episodic migraine patients: an exploratory analysis of a randomized-controlled-trialNiveditha Putananickal, Elena C Gross, Anna-Lena Orsini, et al.BMC Neurology|October 8, 2015
Dysferlinopathy in Switzerland: clinical phenotypes and potential founder effectsJens A Petersen, Thierry Kuntzer, Dirk Fischer, et al.Cephalalgia : an International Journal of Headache|September 20, 2021
Efficacy and safety of exogenous beta-hydroxybutyrate for preventive treatment in episodic migraine: A single-centred, randomised, placebo-controlled, double-blind crossover trialNiveditha Putananickal, Elena C Gross, Anna-Lena Orsini, et al.Journal of Neurology|January 8, 2025
Spinal cord gray matter atrophy is associated with disability in spinal muscular atrophyEva Maria Kesenheimer, Maria Janina Wendebourg, Claudia Weidensteiner, et al.European Journal of Medical Genetics|December 22, 2010
SNP-array based whole genome homozygosity mapping: a quick and powerful tool to achieve an accurate diagnosis in LGMD2 patientsLea Papić, Dirk Fischer, Slave Trajanoski, et al.Human Molecular Genetics|November 20, 2010
Enhanced excitation-coupled Ca(2+) entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with central core diseaseSusan Treves, Mirko Vukcevic, Pierre-Yves Jeannet, et al.Gene|January 14, 2012
High resolution array in the clinical approach to chromosomal phenotypesIsabel Filges, Luzia Suda, Peter Weber, et al.Pageof 10