Longevity in Rett Syndrome: Analysis of the North American Database-Reference-Cited by-同舟云学术

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Longevity in Rett Syndrome: Analysis of the North American Database

Published:2010-01 Issue:1 Volume:156 Page:135-138.e1
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Kirby Russell S.,Lane Jane B.,Childers Jerry,Skinner Steve A.,Annese Fran,Barrish Judy O.,Glaze Daniel G.,MacLeod Patrick,Percy Alan K.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference7 articles.

1. Uber ein eigenartiges hirnatrophisches Syndrom bei Hyperammonamie im Kindesalter;Rett;Wiener Med Wochenschrift,1966

2. 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 2001;Hagberg;Eur J Paediatr Neurol,2002

3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999

4. Rett syndrome: model of neurodevelopmental disorders;Percy;J Child Neurol,2005

5. The incidence of Rett syndrome in France;Bienvenu;Pediatr Neurol,2006

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