Showing results (21-30 of 167) with videos related to
Sort By:
Pageof 17
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.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 1, 1994
Clinical outcome after near-fatal late shunt complication in hydrocephalusI Emanuelson, L von Wendt, M Kyllerman, et al.Acta Neuropathologica|January 1, 1997
Early-infantile galactosialidosis with multiple brain infarctions: morphological, neuropathological and neurochemical findingsC Nordborg, M Kyllerman, N Conradi, et al.Neuropediatrics|April 1, 1993
Benzodiazepine amplification of valproate teratogenic effects in children of mothers with absence epilepsyL Laegreid, M Kyllerman, T Hedner, 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|June 21, 2002
Dysarthria, progressive parkinsonian features and symmetric necrosis of putamen in a family with painful lipomas (Dercum disease variant)M Kyllerman, G Brandberg, L-M Wiklund, 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.Brain & Development|July 1, 1993
Early onset dystonia decreasing with development. Case report of two children with familial myoclonic dystoniaM Kyllerman, G Sanner, L Forsgren, et al.Epilepsia|November 1, 1991
Clinical and neurophysiological development of Unverricht-Lundborg disease in four Swedish siblingsM Kyllerman, K Sommerfelt, A Hedström, et al.Pageof 17