Evidence for distinct genetic influences on generalized and localization-related epilepsy. (Q35112779)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12919389%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Evidence for distinct genetic influences on generalized and localization-related epilepsy (English)

1 reference

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6 November 2019

7

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6 November 2019

5

Timothy A Pedley

1 reference

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6 November 2019

author name string

Melodie Rose Winawer

1

1 reference

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6 November 2019

Daniel Rabinowitz

2

1 reference

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6 November 2019

Christie Barker-Cummings

3

1 reference

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6 November 2019

Mark L Scheuer

4

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6 November 2019

W Allen Hauser

6

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6 November 2019

publication date

1 September 2003

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6 November 2019

1 reference

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6 November 2019

volume

44

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6 November 2019

issue

9

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6 November 2019

page(s)

1176-1182

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Concordance of disease form in kindreds ascertained through affected individuals

6 November 2019

cites work

1 reference

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Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.

9 July 2018

1 reference

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Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

9 July 2018

1 reference

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A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

9 July 2018

1 reference

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Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures

9 July 2018

1 reference

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First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene

9 July 2018

1 reference

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Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

9 July 2018

1 reference

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Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

9 July 2018

1 reference

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Are Generalized and Localization-Related Epilepsies Genetically Distinct?

9 July 2018

1 reference

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

9 July 2018

1 reference

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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

9 July 2018

1 reference

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Genetic Epidemiology of Epilepsy

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1626268

Reliability of seizure classification using a semistructured interview

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1626268

Proposal for revised clinical and electroencephalographic classification of epileptic seizures. From the Commission on Classification and Terminology of the International League Against Epilepsy

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1626268

Seizure risk in offspring of parents with generalized versus partial epilepsy

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1626268

Semistructured interview for seizure classification: agreement with physicians' diagnoses

9 July 2018

1 reference

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9 July 2018

1 reference

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Data collection strategies in genetic epidemiology: The Epilepsy Family Study of Columbia University

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1626268

Epilepsies in twins: genetics of the major epilepsy syndromes

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1626268

The heredity of epilepsy as told by relatives and twins

27 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2003.58902.X

Familial occurrence of epilepsy in children with newly diagnosed multiple seizures: Dutch Study of Epilepsy in Childhood

21 January 2018

1 reference

12 December 2020

Children with familial cryptogenic epilepsy have a favorable seizure prognosis

1 reference

12 December 2020

Occurrence of epilepsies in family members of Indian probands with different epileptic syndromes

1 reference

12 December 2020

Concordance of clinical forms of epilepsy in families with several affected members. Italian League Against Epilepsy Genetic Collaborative Group

1 reference

12 December 2020

10.1046/J.1528-1157.2003.58902.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12919389%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12919389%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

PubMed publication ID

12919389

1 reference