(Q48655789)

English

Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.

scientific article published in February 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q. (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

childhood absence epilepsy

1 reference

based on heuristic

inferred from title

William P Whitehouse

5

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

author name string

Robert Robinson

1

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Nichole Taske

2

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Thomas Sander

3

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Armin Heils

4

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Françoise Goutières

6

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Jean Aicardi

7

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Anna Elina Lehesjoki

8

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Auli Siren

9

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Mogens Laue Friis

10

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Marianne Juel Kjeldsen

11

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Chrysostomos Panayiotopoulos

12

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Colin Kennedy

13

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Colin Ferrie

14

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Michele Rees

15

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

R Mark Gardiner

16

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

publication date

1 February 2002

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Epilepsy Research

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

48

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

3

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

169-179

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells

1 reference

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

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Concepts of absence epilepsies: discrete syndromes or biological continuum?

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7 January 2021

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Epilepsies in twins: genetics of the major epilepsy syndromes.

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7 January 2021

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Segregation analysis in typical absence epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2801%2900335-7

7 January 2021

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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse

1 reference

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7 January 2021

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Genetics. The land between Mendelian and multifactorial inheritance

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7 January 2021

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

1 reference

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7 January 2021

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Association between the alpha(1a) calcium channel gene CACNA1A and idiopathic generalized epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2801%2900335-7

7 January 2021

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Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

1 reference

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7 January 2021

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Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2801%2900335-7

7 January 2021

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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

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7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0920-1211%2801%2900335-7

7 January 2021

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Possible association between childhood absence epilepsy and the gene encoding GABRB3

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https://api.crossref.org/works/10.1016%2FS0920-1211%2801%2900335-7

7 January 2021

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Absence epilepsy in tottering mutant mice is associated with calcium channel defects

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7 January 2021

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Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.

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7 January 2021

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Mechanisms of generalized absence epilepsy

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7 January 2021

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Structure and organization of GABRB3 and GABRA5.

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7 January 2021

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The Human γ-Aminobutyric Acid Receptor Subunit β3 and α5 Gene Cluster in Chromosome 15q11-q13 Is Rich in Highly Polymorphic (CA)n Repeats

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The prevalence and incidence of convulsive disorders in children

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Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

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7 January 2021

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Lack of the burst firing of thalamocortical relay neurons and resistance to absence seizures in mice lacking alpha(1G) T-type Ca(2+) channels

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2801%2900335-7

7 January 2021

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Epilepsy in young people: 23 year follow up of the British national child development study

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7 January 2021

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Strategies for multilocus linkage analysis in humans

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On the action of the anti-absence drug ethosuximide in the rat and cat thalamus.

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7 January 2021

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The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

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Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.

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Radicals r'aging

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Identifiers

10.1016/S0920-1211(01)00335-7

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/11904235

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