The genetic basis of migraine: how much do we know? (Q33774510)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563232%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

review article

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title

The genetic basis of migraine: how much do we know? (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563232%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

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K Gardner

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563232%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

publication date

1 November 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563232%20AND%20SRC:MED&resulttype=core&format=json

Canadian Journal of Neurological Sciences

2 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563232%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

volume

26 Suppl 3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563232%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

page(s)

S37-43

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563232%20AND%20SRC:MED&resulttype=core&format=json

A Population-Based Survey of Headache and Migraine in 22,809 Adults

2 November 2019

cites work

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Familial hemiplegic migraine with irreversible brain damage.

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Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

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7 January 2021

The future of genetic studies of complex human diseases

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7 January 2021

Migraine without aura and migraine with aura are inherited disorders

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7 January 2021

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

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7 January 2021

Genetics of migraine and other headache.

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7 January 2021

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia

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7 January 2021

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

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7 January 2021

Association between dopamine receptor genes and migraine without aura in a Sardinian sample

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7 January 2021

Familial hemiplegic migraine

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7 January 2021

Migraine and concomitant symptoms among 8167 adult twin pairs.

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7 January 2021

Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.

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7 January 2021

Evidence for an X-linked genetic component in familial typical migraine

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7 January 2021

Multiple structural elements in voltage-dependent Ca2+ channels support their inhibition by G proteins

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7 January 2021

Isoform-specific interaction of the alpha1A subunits of brain Ca2+ channels with the presynaptic proteins syntaxin and SNAP-25

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7 January 2021

A new locus for hemiplegic migraine maps to chromosome 1q31

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7 January 2021

Familial risk of migraine: A population-based study

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7 January 2021

Crosstalk between G proteins and protein kinase C mediated by the calcium channel alpha1 subunit.

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7 January 2021

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

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7 January 2021

Genetic risk factors and ischaemic cerebrovascular disease: role of common variation of the genes encoding apolipoproteins and angiotensin-converting enzyme.

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7 January 2021

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

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7 January 2021

Different types of calcium channels mediate central synaptic transmission

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7 January 2021

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

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7 January 2021

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

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7 January 2021

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p

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7 January 2021

Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels

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7 January 2021

Role of calcium channel subtypes in calcium transients in hippocampal CA3 neurons

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7 January 2021

Familial Migraine: Exclusion of the Susceptibility Gene from the Reported Locus of Familial Hemiplegic Migraine on 19p

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7 January 2021

Genetic influence in headaches: a Swedish twin study.

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7 January 2021

Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles

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7 January 2021

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

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7 January 2021

New genetic concepts and stroke prevention

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7 January 2021

Progressive ataxia due to a missense mutation in a calcium-channel gene

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7 January 2021

MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

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7 January 2021

A gene for familial hemiplegic migraine maps to chromosome 19

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7 January 2021

10.1017/S0317167100000184

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563232%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference