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Bengt Hagberg

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Mental Retardation and Developmental Disabilities Research Reviews|July 12, 2002
Clinical manifestations and stages of Rett syndromeBengt Hagberg
Journal of Child Neurology|October 18, 2005
Rett syndrome: long-term clinical follow-up experiences over four decadesBengt Hagberg
Journal of Child Neurology|October 18, 2005
MECP2 abnormality phenotypes: clinicopathologic area with broad variabilityAnna Erlandson, Bengt Hagberg
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 16, 2002
An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001Bengt Hagberg, Folker Hanefeld, Alan Percy, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 19, 2003
Odd MECP2-mutated Rett variant-long-term follow-up profile to age 25Bengt Hagberg, Anna Erlandsson, Mårten Kyllerman, et al.
Genetic Testing|March 6, 2004
Multiplex ligation-dependent probe amplification (MLPA) detects large deletions in the MECP2 gene of Swedish Rett syndrome patientsAnna Erlandson, Lena Samuelsson, Bengt Hagberg, et al.
Journal of Child Neurology|January 8, 2011
Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysisSaideh Rajaei, Anna Erlandson, Marten Kyllerman, et al.
American Journal of Medical Genetics|February 13, 2002
Subtelomeric rearrangements detected in patients with idiopathic mental retardationBritt-Marie Anderlid, Jacqueline Schoumans, Göran Annerén, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Mental Retardation and Developmental Disabilities Research Reviews|July 12, 2002
Clinical manifestations and stages of Rett syndromeBengt Hagberg
Journal of Child Neurology|October 18, 2005
Rett syndrome: long-term clinical follow-up experiences over four decadesBengt Hagberg
Journal of Child Neurology|October 18, 2005
MECP2 abnormality phenotypes: clinicopathologic area with broad variabilityAnna Erlandson, Bengt Hagberg
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 16, 2002
An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001Bengt Hagberg, Folker Hanefeld, Alan Percy, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 19, 2003
Odd MECP2-mutated Rett variant-long-term follow-up profile to age 25Bengt Hagberg, Anna Erlandsson, Mårten Kyllerman, et al.
Genetic Testing|March 6, 2004
Multiplex ligation-dependent probe amplification (MLPA) detects large deletions in the MECP2 gene of Swedish Rett syndrome patientsAnna Erlandson, Lena Samuelsson, Bengt Hagberg, et al.
Journal of Child Neurology|January 8, 2011
Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysisSaideh Rajaei, Anna Erlandson, Marten Kyllerman, et al.
American Journal of Medical Genetics|February 13, 2002
Subtelomeric rearrangements detected in patients with idiopathic mental retardationBritt-Marie Anderlid, Jacqueline Schoumans, Göran Annerén, et al.
Pageof 1