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The genetics of migraine
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
The genetics of migraine.
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
main subject
migraine
1 reference
based on heuristic
inferred from title
author
Marie-Germaine Bousser
series ordinal
3
0 references
Anne Ducros
object named as
Anne Ducros
series ordinal
1
0 references
Elisabeth Tournier-Lasserve
object named as
Elisabeth Tournier-Lasserve
series ordinal
2
0 references
publication date
1 September 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
published in
Lancet Neurology
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
volume
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
page(s)
285-293
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
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Prevalence of migraine headache in the United States. Relation to age, income, race, and other sociodemographic factors
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An update on the epidemiology of migraine
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Crossref
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Prevalence and burden of migraine in the United States: data from the American Migraine Study II.
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Intracranial arteriovenous malformation and migraine
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Crossref
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7 January 2021
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Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
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Crossref
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7 January 2021
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MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission
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Antiphospholipid syndrome: clinical and immunologic manifestations and patterns of disease expression in a cohort of 1,000 patients
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New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature
1 reference
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Crossref
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7 January 2021
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Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Is familial hemiplegic migraine a hereditary form of basilar migraine?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial migraine coma: a case study
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine, nystagmus, and cerebellar atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrent Episodes of Coma: An Unusual Phenotype of Familial Hemiplegic Migraine with Linkage to Chromosome 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic heterogeneity of familial hemiplegic migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetics of migraine without aura and migraine with aura
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Headache in a non-clinic twin population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine in twins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine and concomitant symptoms among 8167 adult twin pairs.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic influence in headaches: a Swedish twin study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine in twins raised together and apart
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine without aura: A population-based twin study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
The relative role of genetic and environmental factors in migraine without aura
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
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7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence of a genetic factor in migraine with aura: a population-based Danish twin study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine: Intelligence, Social Class, and Familial Prevalence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine in patients attending a migraine clinic: an analysis by computer of age, sex and family history
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics of migraine and migraine accompagneé: a study of eighty-one children and their families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Testing Models for Genetic Determination in Migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A 40-year follow-up of school children with migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increased familial risk and evidence of genetic factor in migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial risk of migraine: A population-based study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inheritance of migraine investigated by complex segregation analysis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of 31 families with an apparently autosomal-dominant transmission of migraine with aura in the nuclear family.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association studies of genetic polymorphisms and complex disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for familial hemiplegic migraine maps to chromosome 19
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new locus for hemiplegic migraine maps to chromosome 1q31
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular and functional diversity of voltage-gated calcium channels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three for T: molecular analysis of the low voltage-activated calcium channel family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca(2+) channel mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Splicing of alpha 1A subunit gene generates phenotypic variants of P- and Q-type calcium channels.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic heterogeneity in Italian families with familial hemiplegic migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A nosographic analysis of the migraine aura in a general population.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impairment of neuromuscular transmission in a subgroup of migraine patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuromuscular transmission in migraine: a single-fiber EMG study in clinical subgroups.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Migraine: Exclusion of the Susceptibility Gene from the Reported Locus of Familial Hemiplegic Migraine on 19p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Searching for migraine genes: exclusion of 290 cM out of the whole human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Investigation of theCACNA1A gene as a candidate for typical migraine susceptibility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for an X-linked genetic component in familial typical migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A susceptibility locus for migraine with aura, on chromosome 4q24.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A typical migraine susceptibility region localizes to chromosome 1q31
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetics of migraine headaches: a review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association between dopamine receptor genes and migraine without aura in a Sardinian sample
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Significance of serotonin transporter gene polymorphism in migraine.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Significance of the catechol-O-methyltransferase gene polymorphism in migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association between migraine and endothelin type A receptor (ETA -231 A/G) gene polymorphism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1474-4422(02)00134-5
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
PubMed ID
12849426
1 reference
stated in
Europe PubMed Central
PubMed ID
12849426
retrieved
6 August 2017
ResearchGate publication ID
10672388
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