Rett Syndrome: Recognition of Facial Expression and Its Relation to Scanning Patterns-Reference-Cited by-同舟云学术

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Rett Syndrome: Recognition of Facial Expression and Its Relation to Scanning Patterns

Published:2014-11 Issue:5 Volume:51 Page:650-656
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Djukic Aleksandra,Rose Susan A.,Jankowski Jeffery J.,Feldman Judith F.

Funder

International Rett Syndrome Foundation

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference34 articles.

1. On a unusual brain atrophy syndrome in hyperammonemia in childhood;Rett;Wien Med Wochenschr,1966

2. The story of Rett syndrome: from clinic to neurobiology;Chahrour;Neuron,2007

3. Rett syndrome: revised diagnostic criteria and nomenclature;Neul;Ann Neurol,2010

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

5. MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution;Kaufmann;Brain Dev,2005

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