Rett syndrome before regression: A time window of overlooked opportunities for diagnosis and intervention-Reference-Cited by-同舟云学术

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Rett syndrome before regression: A time window of overlooked opportunities for diagnosis and intervention

Published:2019-12 Issue: Volume:107 Page:115-135
ISSN:0149-7634
Container-title:Neuroscience & Biobehavioral Reviews
language:en
Short-container-title:Neuroscience & Biobehavioral Reviews

Author:

Cosentino Livia,Vigli Daniele,Franchi Francesca,Laviola Giovanni,De Filippis Bianca^ORCID

Funder

Jerome Lejeune Foundation (France) and AIRETT (Italy) to G.L.

Italian Ministry of Health

University of Pennsylvania Orphan Disease Center (USA) on behalf of LouLou Foundation to B.D.F

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Cognitive Neuroscience,Neuropsychology and Physiological Psychology

Reference124 articles.

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

2. Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome;Asaka;Neurobiol. Dis.,2006

3. Defects during Mecp2 null embryonic cortex development precede the onset of overt neurological symptoms;Bedogni;Cereb. Cortex,2016

4. Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome;Belichenko;J. Comp. Neurol.,2008

5. Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks;Belichenko;J. Comp. Neurol.,2009

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