Epilepsy and mental retardation limited to females: an under-recognized disorder (Q29039028)

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1 January 2020

title

Epilepsy and mental retardation limited to females: an under-recognized disorder (English)

2 references

27 March 2017

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1

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Leanne Dibbens

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Amos D. Korczyn

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Jozef Gécz

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Samuel Berkovic

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Dorit Lev

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Tally Lerman-Sagie

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Hans-Hilger Ropers

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author name string

Samantha J Turner

2

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Marta A Bayly

4

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Kathryn Friend

5

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Bree Hodgson

6

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Linda Burrows

7

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Marie Shaw

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Chen Wei

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Reinhard Ullmann

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Pierre Szepetowski

12

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Eric Haan

13

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Aziz Mazarib

14

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Zaid Afawi

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Miriam Y Neufeld

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P Ian Andrews

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Geoffrey Wallace

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Sara Kivity

19

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Christopher P Derry

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John C Mulley

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language of work or name

English

0 references

publication date

29 January 2008

1 reference

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1 January 2020

2 references

27 March 2017

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volume

131

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page(s)

918-927

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issue

Pt 4

1 reference

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A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

1 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

Seizures and electroencephalographic findings in CDKL5 mutations: case report and review

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

The spectrum of SCN1A-related infantile epileptic encephalopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

A new familial form of convulsive disorder and mental retardation limited to females

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

Autism, regression, and the broader autism phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

Variable expression of the autism broader phenotype: findings from extended pedigrees.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

Validation of a questionnaire for clinical seizure diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

Clinical and genetic aspects of craniofrontonasal syndrome: towards resolving a genetic paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

Rett syndrome: new clinical and molecular insights.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWM338

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWM338

3 references

27 March 2017

Consolidated OpenCitations Corpus – April 2017

1163471

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1163471

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

1163471