State‐of‐the‐art therapies for Rett syndrome-Reference-Cited by-同舟云学术

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State‐of‐the‐art therapies for Rett syndrome

Published:2022-09-03 Issue:2 Volume:65 Page:162-170
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Develop Med Child Neuro

Author:

Panayotis Nicolas¹²³^ORCID,Ehinger Yann⁴,Felix Marie Solenne⁵,Roux Jean‐Christophe⁵^ORCID

Affiliation:

1. Department of Biomolecular Sciences Weizmann Institute of Science Rehovot Israel

2. Department of Molecular Neuroscience Weizmann Institute of Science Rehovot Israel

3. Université Paris Cité, CNRS, Saints‐Pères Paris Institute for the Neurosciences Paris France

4. Department of Neurology University of California San Francisco San Francisco CA USA

5. MMG, INSERM Aix Marseille University Marseille France

Funder

French Muscular Dystrophy Association

Institut National de la Santé et de la Recherche Médicale

International Rett Syndrome Foundation

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.15383

Reference81 articles.

1. On a unusual brain atrophy syndrome in hyperammonemia in childhood;Rett A.;Wiener medizinische Wochenschrift,1966

2. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases

3. Rett syndrome: think outside the (skull) box

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

5. Rett syndrome: a complex disorder with simple roots

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