(Q30681069)

26 June 2017

title

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

1 reference

familial temporal lobe epilepsy

26 June 2017

main subject

temporal lobe epilepsy

1 reference

based on heuristic

inferred from title

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3

Karl O Nakken

1 reference

26 June 2017

Eylert Brodtkorb

1

1 reference

26 June 2017

Wenli Gu

series ordinal

2

1 reference

26 June 2017

Christine Fischer

series ordinal

4

1 reference

26 June 2017

Ortrud K Steinlein

series ordinal

5

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26 June 2017

publication date

1 March 2002

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26 June 2017

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26 June 2017

volume

43

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26 June 2017

issue

3

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26 June 2017

page(s)

228-235

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Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder

26 June 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.32001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.32001.X

Localization of a gene for partial epilepsy to chromosome 10q

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.32001.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/10.1046%2FJ.1528-1157.2002.32001.X

Autosomal dominant partial epilepsy with auditory features: defining the phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.32001.X

Autosomal dominant partial epilepsy with auditory features: description of a new family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.32001.X

A potassium channel mutation in neonatal human epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.32001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.32001.X

Autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.32001.X

10.1046/J.1528-1157.2002.32001.X

21 January 2018

Identifiers

DOI

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26 June 2017

1 reference