Molecular genetics of migraine headaches: a review (Q33922114)

30 July 2017

1 reference

title

Molecular genetics of migraine headaches: a review (English)

1 reference

30 July 2017

1 reference

1 reference

P Montagna

1

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PubMed ID

10817441

30 July 2017

language of work or name

English

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publication date

1 February 2000

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30 July 2017

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30 July 2017

20

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30 July 2017

3-14

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30 July 2017

1

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Segregation analysis of migraine in 128 families

30 July 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Genetic transmission of migraine without aura: a study of 68 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Familial occurrence of migraine without aura and migraine with aura.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

The genetics of migraine without aura and migraine with aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Genetic influence in headaches: a Swedish twin study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Inheritance of migraine investigated by complex segregation analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Migraine with aura: segregation analysis and heritability estimation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

A gene for familial hemiplegic migraine maps to chromosome 19

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.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.1468-2982.2000.00003.X

Increased therapeutic efficacy with rt-PA and anti-CD18 antibody treatment of stroke in the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Genetic heterogeneity in Italian families with familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

A new locus for hemiplegic migraine maps to chromosome 1q31

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.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.1468-2982.2000.00003.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Effects of serotonin on caudal raphe neurons: inhibition of N- and P/Q-type calcium channels and the afterhyperpolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.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.1468-2982.2000.00003.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.1468-2982.2000.00003.X

Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Downbeat nystagmus in two siblings with spinocerebellar ataxia type 6 (SCA 6).

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

21 January 2018

Migraine and epilepsy

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Familial migraine with vertigo: no mutations found in CACNA1A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Mitochondrial DNA in migraine with aura.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Search for Mitochondrial Dna Mutations in Migraine Subgroups

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Migraine association and linkage analyses of the human 5-hydroxytryptamine (5HT2A) receptor gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Allelic variation in the serotonin 5-HT2C receptor gene and migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

The transition G to A at position 20210 in the 3'-untranslated region of the prothrombin gene is not associated with migrainous infarction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Migraine and prothrombotic genetic risk factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

The comorbid association of migraine with osteoarthritis and hypertension: complement C3F and Berkson's bias

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Phenotypic variability of CADASIL and novel morphologic findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Familial vestibulopathy: a new dominantly inherited syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Brain excitability in migraine: evidence from transcranial magnetic stimulation studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Testing Models for Genetic Determination in Migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Monozygotic twins discordant for familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

Lack of association between mitochondrial tRNALeu(UUR) point mutation and cluster headache

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-2982.2000.00003.X

10.1046/J.1468-2982.2000.00003.X

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference

PubMed ID

10817441