(Q50472611)

14 March 2018

title

Speech-induced aphasic seizures in epilepsy caused by LGI1 mutation. (English)

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14 March 2018

author name string

Eylert Brodtkorb

1

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14 March 2018

Ralf P Michler

2

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14 March 2018

Wenli Gu

3

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14 March 2018

Ortrud K Steinlein

4

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14 March 2018

publication date

1 June 2005

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14 March 2018

published in

Epilepsia

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14 March 2018

volume

46

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14 March 2018

page(s)

963-966

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14 March 2018

issue

6

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14 March 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

A novel gene causing a mendelian audiogenic mouse epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

Autosomal dominant partial epilepsy with auditory features: defining the phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

LGI1 mutations in autosomal dominant partial epilepsy with auditory features

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

Telephone-induced seizures: a new type of reflex epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

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/10.1111%2FJ.1528-1167.2005.47104.X

Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.47104.X

10.1111/J.1528-1167.2005.47104.X

21 January 2018

Identifiers

DOI

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14 March 2018

PubMed ID

15946341

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14 March 2018