(Q47962832)

English

Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing.

scientific article published in March 2003

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

based on heuristic

inferred from title

familial hemiplegic migraine

1 reference

based on heuristic

inferred from title

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

author name string

Thomas Wieser

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Christoph Mueller

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Stefan Evers

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Stephan Zierz

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

publication date

1 March 2003

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Clinical Chemistry and Laboratory Medicine

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

41

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

272-275

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

The genetics of migraine without aura and migraine with aura

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Migraine and concomitant symptoms among 8167 adult twin pairs.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Genetic influence in headaches: a Swedish twin study.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Evidence of a genetic factor in migraine with aura: a population-based Danish twin study

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Clinical and neuropathological characteristics of hippocampal sclerosis: a community-based study

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Is the CACNA1A gene involved in familial migraine with aura?

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Familial migraine with vertigo: no mutations found in CACNA1A.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Burden of migraine in the United States: disability and economic costs.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.042

21 January 2018

Identifiers

10.1515/CCLM.2003.042

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12705332%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

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