Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Kyllerman

Showing results (31-40 of 80) with videos related to

Pageof 8
Sort By:
Helvetica Paediatrica Acta|December 1, 1984
Delineation of a characteristic phenotype in distal trisomy 2qM Kyllerman, J Wahlström, B Westerberg, et al.
Pediatric Neurology|February 1, 1996
Autism in Angelman syndrome: a population-based studyS Steffenburg, C L Gillberg, U Steffenburg, 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.
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.
Pageof 8

Showing results (31-40 of 80) with videos related to

Sort By:
Pageof 8
Helvetica Paediatrica Acta|December 1, 1984
Delineation of a characteristic phenotype in distal trisomy 2qM Kyllerman, J Wahlström, B Westerberg, et al.
Pediatric Neurology|February 1, 1996
Autism in Angelman syndrome: a population-based studyS Steffenburg, C L Gillberg, U Steffenburg, 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.
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.
Pageof 8