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Neuromuscular Disorders : NMD|March 11, 2000
Neuromuscular disorders in childhood: a descriptive epidemiological study from western SwedenN Darin, M TuliniusEuropean Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2001
Muscle strength and motor function in children and adolescents with spinal muscular atrophy II and IIIA K Kroksmark, E Beckung, M TuliniusNeuromuscular Disorders : NMD|July 23, 1998
Threshold expression of the tRNA(Lys) A8344G mutation in single muscle fibresA R Moslemi, M Tulinius, E Holme, et al.Acta Neuropathologica|January 1, 1995
Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibresA Oldfors, E Holme, M Tulinius, et al.Neurology|March 7, 2007
Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutationH Tajsharghi, E Kimber, D Holmgren, et al.Acta Neuropathologica|January 1, 1989
Cytochrome c oxidase deficiency in infancyA Oldfors, H Sommerland, E Holme, et al.Pediatric Radiology|January 1, 1993
A case of Kearns-Sayre syndrome with metaphyseal dysplasiaB Wilson, I Claësson, C Forsell, et al.Annals of Neurology|March 23, 2001
The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalitiesN Darin, A Oldfors, A R Moslemi, et al.Neurology|August 23, 2006
A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposisE Kimber, H Tajsharghi, A-K Kroksmark, et al.Pediatric Research|August 1, 1990
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndromeN G Larsson, E Holme, B Kristiansson, et al.Pageof 3