(Q46051669)

19 December 2017

title

Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13). (English)

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19 December 2017

spinocerebellar ataxia type 13

main subject

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based on heuristic

inferred from title

temporal lobe epilepsy

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2

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19 December 2017

Wolfgang H. Oertel

7

object named as

Wolfgang H Oertel

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19 December 2017

9

Felix Rosenow

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19 December 2017

Hajo Hamer

8

object named as

Hajo M Hamer

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19 December 2017

author name string

Katrin Bürk

1

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19 December 2017

Philipp S Reif

3

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19 December 2017

Karla P Figueroa

4

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19 December 2017

Stefan M Pulst

5

1 reference

19 December 2017

Christine Zühlke

6

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19 December 2017

publication date

29 January 2013

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19 December 2017

International Journal of Neuroscience

published in

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19 December 2017

volume

123

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19 December 2017

issue

4

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19 December 2017

page(s)

278-282

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19 December 2017

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

1 reference

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

Presurgical evaluation of epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

Allele-dependent changes of olivocerebellar circuit properties in the absence of the voltage-gated potassium channels Kv3.1 and Kv3.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

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/10.3109%2F00207454.2012.755180

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00207454.2012.755180

10.3109/00207454.2012.755180

21 January 2018

Identifiers

DOI

1 reference

19 December 2017

1 reference

19 December 2017