(Q54589200)

1 June 2018

title

Neurodevelopmental disorders: Clinical criteria for Rett syndrome. (English)

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1 June 2018

neurodevelopmental disorder

main subject

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Sakkubai Naidu

1

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1 June 2018

Michael V Johnston

series ordinal

2

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1 June 2018

language of work or name

English

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publication date

17 May 2011

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1 June 2018

published in

Nature Reviews Neurology

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1 June 2018

volume

7

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1 June 2018

issue

6

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1 June 2018

page(s)

312-314

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1 June 2018

https://scigraph.springernature.com/pub.10.1038/nrneurol.2011.64

exact match

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cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Rett syndrome diagnostic criteria: lessons from the Natural History Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Rett syndrome: revised diagnostic criteria and nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Key clinical features to identify girls with CDKL5 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

MECP2 mutations in males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Identification of cis-regulatory elements for MECP2 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.64

31 March 2020

Identifiers

DOI

10.1038/NRNEUROL.2011.64

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1 June 2018

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1 June 2018