Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. (Q48771735)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

title

Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

author

José Félix Martí Massó

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

Jacques S Beckmann

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

Adolfo López de Munain

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

author name string

J J Poza

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

A Sáenz

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

A Martínez-Gil

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

N Cheron

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

A M Cobo

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

M Urtasun

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

D Grid

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

J F Prud'homme

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

publication date

1 February 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

volume

45

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

page(s)

182-188

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

12 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

A potassium channel mutation in neonatal human epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Localization of a gene for partial epilepsy to chromosome 10q

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Computer-simulation methods in human linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Strategies for multilocus linkage analysis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Single photon emission computed tomography in epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Febrile convulsions. Is seizure duration the most important predictor of temporal lobe epilepsy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Temporal lobe epilepsy caused by mesial temporal sclerosis and temporal neocortical lesions. A clinical and electroencephalographic study of 46 pathologically proven cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Temporal lobe epilepsy in childhood: Clinical, EEG, and neuroimaging findings and syndrome classification in a cohort with new-onset seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Musicogenic epilepsy: review of the literature and case report with ictal single photon emission computed tomography

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

Autosomal dominant rolandic epilepsy and speech dyspraxia: A new syndrome with anticipation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989620 AND SRC:MED&resulttype=core&format=json

12 December 2019

1 reference