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Acta Neurologica Scandinavica|March 12, 2014
Ocular, bulbar, limb, and cardiopulmonary involvement in oculopharyngeal muscular dystrophyN Witting, A Mensah, L Køber, et al.Neurology|September 26, 2002
Multiple mtDNA deletions with features of MNGIEJ Vissing, K Ravn, E R Danielsen, et al.Neurology|June 20, 1998
A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intoleranceJ Vissing, M B Salamon, P Arlien-Søborg, et al.Journal of Medical Genetics|February 24, 2006
Tissue specific distribution of the 3243A->G mtDNA mutationA L Frederiksen, P H Andersen, K O Kyvik, et al.Journal of Ethnopharmacology|February 19, 2017
Screening of plants used in the European traditional medicine to treat memory disorders for acetylcholinesterase inhibitory activity and anti amyloidogenic activityEva S B Lobbens, Karina J Vissing, Lene Jorgensen, et al.European Journal of Neurology|October 6, 2015
Prevalence of migraine in persons with the 3243A>G mutation in mitochondrial DNAS Guo, A-L Esserlind, Z Andersson, et al.The American Journal of Physiology|October 12, 1999
Differential effects from parapyramidal region and rostral ventrolateral medulla mediated by substance PK Swiatkowski, L M Dellamano, J Vissing, et al.Journal of Neurology|December 12, 2024
Factors affecting the diagnostic delay of myasthenia gravisI R Marlet, R K Andersen, K H Axelsen, et al.The Journal of Clinical Endocrinology and Metabolism|February 22, 2013
Patients with medium-chain acyl-coenzyme a dehydrogenase deficiency have impaired oxidation of fat during exercise but no effect of L-carnitine supplementationK L Madsen, N Preisler, M C Orngreen, et al.European Journal of Neurology|May 20, 2014
Risk of cancer in relatives of patients with myotonic dystrophy: a population-based cohort studyM Lund, L J Diaz, S Gørtz, et al.Pageof 8