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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.
Neuropediatrics|November 10, 2004
Large-cell medulloblastoma in Aicardi syndrome. Case report and literature reviewL Palmér, C Nordborg, K Steneryd, et al.
European Child & Adolescent Psychiatry|December 1, 1996
Maternal origin of inv dup(15) chromosomes in infantile autismT Martinsson, T Johannesson, M Vujic, et al.
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