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Neuropediatrics|June 1, 1994
Analysis of glial fibrillary acidic protein in the cerebrospinal fluid of children investigated for encephalopathyS Ehlers, M Kyllerman, L RosengrenNeuropediatrics|January 20, 2007
Male Rett phenotypes in T158M and R294X MeCP2-mutationsM Lundvall, L Samuelsson, M KyllermanEpilepsy Research|November 1, 1992
Neurovascular microdysgenesis in a case of Unverricht-Lundborg's diseaseC Nordborg, E Ben-Menachem, M KyllermanEpilepsy Research|April 20, 2000
Superoxide dismutase and glutathione peroxidase function in progressive myoclonus epilepsiesE Ben-Menachem, M Kyllerman, S MarklundScandinavian Journal of Rheumatology|November 10, 1998
Fibromyalgia in hyperkalemic periodic paralysisF R Götze, S Thid, M KyllermanJournal of Child Psychology and Psychiatry, and Allied Disciplines|July 1, 1988
Monozygotic female twins with autism and the fragile-X syndrome (AFRAX)C Gillberg, V A Ohlson, J Wahlström, et al.Human Genetics|January 1, 1985
Unequal mitotic sister chromatid exchange and different length of Y chromosomesJ Wahlström, M Kyllerman, A Hansson, et al.Neuropediatrics|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.Helvetica Paediatrica Acta|December 1, 1984
Delineation of a characteristic phenotype in distal trisomy 2qM Kyllerman, J Wahlström, B Westerberg, et al.Neuropediatrics|October 12, 2005
Increased levels of GFAP in the cerebrospinal fluid in three subtypes of genetically confirmed Alexander diseaseM Kyllerman, L Rosengren, L-M Wiklund, et al.Pageof 9