(Q51970363)

19 April 2018

title

Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene. (English)

1 reference

19 April 2018

alternating hemiplegia of childhood

1 reference

1 reference

based on heuristic

inferred from title

familial hemiplegic migraine

1 reference

J Haan

1

1 reference

19 April 2018

E E Kors

2

1 reference

19 April 2018

G M Terwindt

3

1 reference

19 April 2018

F L Vermeulen

4

1 reference

19 April 2018

M N Vergouwe

5

1 reference

19 April 2018

A M van den Maagdenberg

6

1 reference

19 April 2018

D S Gill

7

1 reference

19 April 2018

J Pascual

8

1 reference

19 April 2018

R A Ophoff

9

1 reference

19 April 2018

R R Frants

10

1 reference

19 April 2018

Ferrari

11

1 reference

19 April 2018

language of work or name

English

0 references

publication date

1 October 2000

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19 April 2018

published in

Cephalalgia

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19 April 2018

volume

20

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19 April 2018

issue

8

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19 April 2018

page(s)

696-700

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19 April 2018

A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Benign familial nocturnal alternating hemiplegia of childhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Genetics of primary headaches

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

A new locus for hemiplegic migraine maps to chromosome 1q31

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

A case of alternating hemiplegia of childhood with cerebellar atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Alternating hemiplegia of childhood: report of a case having a long history.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Alternating hemiplegia of childhood: insights into its pathophysiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Chromosomal localization of the human genes for alpha 1A, alpha 1B, and alpha 1E voltage-dependent Ca2+ channel subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

Genetic heterogeneity in Italian families with familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0333-1024.2000.00095.X

10.1046/J.0333-1024.2000.00095.X

21 January 2018

Identifiers

DOI

1 reference

19 April 2018

release_wnkeq2wzfzb4xlrkju73k74v6e

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/wnkeq2wzfzb4xlrkju73k74v6e

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

19 April 2018