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Neuromuscular Disorders : NMD|March 11, 2000
Neuromuscular disorders in childhood: a descriptive epidemiological study from western SwedenN Darin, M TuliniusDevelopmental Medicine and Child Neurology|January 20, 1998
Changes in prevalence, aetiology, age at detection, and associated disabilities in preschool children with hearing impairment born in GöteborgN Darin, P Hanner, K ThiringerNeuropediatrics|December 1, 1994
Clinical, serological and PCR evidence of cytomegalovirus infection in the central nervous system in infancy and childhoodN Darin, T Bergström, A Fast, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 21, 2004
Myopathies associated with myosin heavy chain mutationsA Oldfors, H Tajsharghi, N Darin, et al.Neuromuscular Disorders : NMD|September 1, 2004
Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1)M Ohlsson, H Tajsharghi, N Darin, et al.Annals of Neurology|August 26, 1998
Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuolesN Darin, M Kyllerman, J Wahlström, et al.Neuropediatrics|October 12, 2005
Two new mutations in the MTATP6 gene associated with Leigh syndromeA-R Moslemi, N Darin, M Tulinius, 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.Acta Neurologica Scandinavica|July 10, 2004
The effects of endurance training in persons with a hereditary myosin myopathyK S Sunnerhagen, N Darin, H Tajsharghi, et al.American Journal of Human Genetics|April 17, 1999
Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1T Martinsson, N Darin, M Kyllerman, et al.Pageof 3