Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
Neuropediatrics|January 20, 2007
Male Rett phenotypes in T158M and R294X MeCP2-mutationsM Lundvall, L Samuelsson, M Kyllerman
Epilepsy Research|November 1, 1992
Neurovascular microdysgenesis in a case of Unverricht-Lundborg's diseaseC Nordborg, E Ben-Menachem, M Kyllerman
Epilepsy Research|April 20, 2000
Superoxide dismutase and glutathione peroxidase function in progressive myoclonus epilepsiesE Ben-Menachem, M Kyllerman, S Marklund
Scandinavian Journal of Rheumatology|November 10, 1998
Fibromyalgia in hyperkalemic periodic paralysisF R Götze, S Thid, M Kyllerman
Journal 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.
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