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Neuropediatrics|December 7, 2007
Aicardi syndrome: follow-up investigation of Swedish children born in 1975-2002L Palmér, B Zetterlund, A-L Hård, et al.Acta Neuropathologica|September 8, 2001
Distal infantile neuroaxonal dystrophy--a new familial variant with perineuronal argyrophilic bodiesM Kyllerman, J E Månsson, M Lichtenstein, et al.Acta Paediatrica Scandinavica|July 1, 1982
Dyskinetic cerebral palsy. I. Clinical categories, associated neurological abnormalities and incidencesM Kyllerman, B Bager, J Bensch, et al.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.Pageof 17