(Q57808240)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20864493%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

title

Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance (English)

1 reference

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14 February 2020

1 reference

temporal lobe epilepsy

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1

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14 February 2020

Ingrid Scheffer

2

1 reference

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14 February 2020

Mark J. Cook

4

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14 February 2020

Jacinta M McMahon

8

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14 February 2020

Anne M. McIntosh

10

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14 February 2020

Samuel Berkovic

11

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14 February 2020

author name string

Isabella Taylor

3

1 reference

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14 February 2020

Penelope A McKelvie

5

1 reference

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14 February 2020

Danya F Vears

6

1 reference

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14 February 2020

Kate M Lawrence

7

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14 February 2020

Bronwyn E Grinton

9

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14 February 2020

language of work or name

English

0 references

publication date

23 September 2010

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14 February 2020

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14 February 2020

volume

133

1 reference

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14 February 2020

issue

11

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14 February 2020

page(s)

3221-3231

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Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31.

14 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Epilepsies in twins: genetics of the major epilepsy syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

LGI1 mutations in temporal lobe epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Novel locus on chromosome 12q22-q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Hippocampal volumetric and morphometric studies in frontal and temporal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Clinical course and prognosis of temporal lobe epilepsy. A survey of 666 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Familial temporal lobe epilepsy autosomal dominant inheritance in a large pedigree from southern Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

MRI-based hippocampal volumetrics: data acquisition, normal ranges, and optimal protocol

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Epileptology of the first-seizure presentation: a clinical, electroencephalographic, and magnetic resonance imaging study of 300 consecutive patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Seizure outcome and hippocampal atrophy in familial mesial temporal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

MRI evidence of mesial temporal sclerosis in sporadic "benign" temporal lobe epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

A neurologist's guide to genome-wide association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Localization of a gene for partial epilepsy to chromosome 10q

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

LGI1 mutations in autosomal dominant partial epilepsy with auditory features

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

LGI1 is a Nogo receptor 1 ligand that antagonizes myelin-based growth inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

Genetics of temporal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWQ251

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWQ251

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20864493%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference