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European Journal of Neurology|March 22, 2008
No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutationsL E Hjermind, J Vissing, F Asmus, et al.Clinical Genetics|December 22, 2017
Lecocytes mutation load declines with age in carriers of the m.3243A>G mutation: A 10-year Prospective CohortJ H Langdahl, M Larsen, M Frost, et al.Neurology|February 25, 2009
Fat metabolism during exercise in patients with McArdle diseaseM C Ørngreen, T D Jeppesen, S Tvede Andersen, et al.Neurology|January 13, 2012
Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease?N Preisler, M C Orngreen, A Echaniz-Laguna, et al.Neuromuscular Disorders : NMD|April 19, 2020
No effect of oral sucrose or IV glucose during exercise in phosphorylase b kinase deficiencyA G Andersen, M C Ørngreen, D E T Raaschou-Pedersen, et al.Neurology. Genetics|October 22, 2016
Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)S T Oestergaard, T Stojkovic, J R Dahlqvist, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 24, 2010
McArdle disease: a clinical reviewR Quinlivan, J Buckley, M James, et al.European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.Acta Neurologica Scandinavica|August 24, 2017
Screening for late-onset Pompe disease in western DenmarkJ S Hansen, E G Pedersen, D Gaist, et al.Neurology|April 11, 2008
Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?M C Ørngreen, H J Schelhaas, T D Jeppesen, et al.Pageof 8