Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study-Reference-Cited by-同舟云学术

Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study

Published:2020-06-29 Issue:2 Volume:88 Page:396-406
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol

Author:

Cutri‐French Clare¹^ORCID,Armstrong Dallas²,Saby Joni³,Gorman Casey²,Lane Jane⁴,Fu Cary⁵,Peters Sarika U.⁵,Percy Alan⁵,Neul Jeffrey L.²^ORCID,Marsh Eric D.¹²^ORCID

Affiliation:

1. Perelman School of Medicine at the University of Pennsylvania Philadelphia Pennsylvania

2. Division of Child Neurology Children's Hospital of Philadelphia Philadelphia Pennsylvania

3. Division of Radiology Research Children's Hospital of Philadelphia Philadelphia Pennsylvania

4. Department of Pediatrics, Civitan International Research Center University of Alabama at Birmingham Birmingham Alabama

5. Department of Pediatrics, Vanderbilt Kennedy Center Vanderbilt University Medical Center Nashville Tennessee

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.25797

Reference40 articles.

1. SwaimanKF AshwalS FerrieroDM et al. Swaiman's pediatric neurology: principles and practice. 2018. Available at:https://www.worldcat.org/title/swaimans-pediatric-neurology-principles-and-practice/oclc/988768908. Accessed September 2018.

2. Rett syndrome: Revised diagnostic criteria and nomenclature

3. Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

4. Rett syndrome in Australia: A review of the epidemiology

5. Methyl-CpG-binding protein 2(MECP2) mutation type is associated with disease severity in Rett syndrome

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