Showing results (61-70 of 85) with videos related to
Sort By:
Pageof 9
Annals of Neurology|May 1, 1994
Diagnosis of Epstein-Barr virus-induced central nervous system infections by DNA amplification from cerebrospinal fluidM Landgren, M Kyllerman, T Bergström, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1990
Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variationM Kyllerman, L Forsgren, G Sanner, et al.Acta Neuropathologica|January 1, 1991
Late-infantile Gaucher disease in a child with myoclonus and bulbar signs: neuropathological and neurochemical findingsN Conradi, M Kyllerman, J E Månsson, et al.Acta Paediatrica Scandinavica|April 1, 1990
Rapidly progressive type III Gaucher disease: deterioration following partial splenectomyM Kyllerman, N Conradi, J E Månsson, 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.Acta Neuropathologica|July 27, 2000
Multiple mitochondrial DNA deletions in hereditary inclusion body myopathyM Jansson, N Darin, M Kyllerman, et al.Neuropediatrics|November 1, 1990
Central nervous system malformations and white matter changes in pseudo-neonatal adrenoleukodystrophyM Kyllerman, S Blomstrand, J E Månsson, et al.Journal of Medical Genetics|September 6, 2005
Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)J Schoumans, C Ruivenkamp, E Holmberg, et al.European Child & Adolescent Psychiatry|December 1, 1996
Transient psychosis in a girl with epilepsy and continuous spikes and waves during slow sleep (CSWS)M Kyllerman, A Nydén, N Praquin, et al.Acta Paediatrica Scandinavica|January 1, 1985
Children of alcoholic mothers. Growth and motor performance compared to matched controlsM Kyllerman, M Aronson, K G Sabel, et al.Pageof 9