(Q34981965)

5 August 2017

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title

Molecular genetics of migraine (English)

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5 August 2017

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Arn van den Maagdenberg

series ordinal

object named as

Arn M J M van den Maagdenberg

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Boukje de Vries

series ordinal

object named as

Boukje de Vries

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Michel Ferrari

series ordinal

object named as

Michel D Ferrari

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5 August 2017

Rune R Frants

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5 August 2017

Boukje de Vries

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5 August 2017

publication date

20 May 2009

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5 August 2017

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5 August 2017

volume

126

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5 August 2017

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5 August 2017

page(s)

115-132

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

5 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00439-009-0684-Z

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants

21 January 2018

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Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine

21 January 2018

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The prevalence and characteristics of migraine in a population-based cohort: the GEM study

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00439-009-0684-Z

A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00439-009-0684-Z

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00439-009-0684-Z

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

21 January 2018

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Comorbidity of migraine and epilepsy

21 January 2018

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Association between the tumor necrosis factor-alpha -308 G/A gene polymorphism and migraine

21 January 2018

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Increased familial risk and evidence of genetic factor in migraine

21 January 2018

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Ion regulation in the brain: implications for pathophysiology

21 January 2018

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Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine

21 January 2018

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CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

21 January 2018

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Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk

21 January 2018

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12 December 2020

Localization of a gene for migraine without aura to chromosome 4q21.

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12 December 2020

A nosographic analysis of the migraine aura in a general population.

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12 December 2020

The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online

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12 December 2020

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit

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12 December 2020

Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine Patients

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12 December 2020

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine.

1 reference

12 December 2020

Multilocus analyses reveal involvement of the ESR1, ESR2, and FSHR genes in migraine

1 reference

12 December 2020

The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition

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12 December 2020

Migraine with aura and migraine without aura are not distinct entities: further evidence from a large Dutch population study

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12 December 2020

Association study of a functional variant in intron 8 of the dopamine transporter gene and migraine susceptibility

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12 December 2020

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy

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12 December 2020

ACE D/I polymorphism, migraine, and cardiovascular disease in women

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12 December 2020

Epilepsy as part of the phenotype associated with ATP1A2 mutations

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12 December 2020

Genomewide significant linkage to migrainous headache on chromosome 5q21.

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12 December 2020

C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

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12 December 2020

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura

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12 December 2020

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

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12 December 2020

Minor Head Trauma–Induced Sporadic Hemiplegic Migraine Coma

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12 December 2020

Polymorphisms in the renin-angiotensin system and migraine in women

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12 December 2020

Neuropsychological measures probably facilitate heritability research of ADHD.

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12 December 2020

Identification of a specific role for the Na,K-ATPase alpha 2 isoform as a regulator of calcium in the heart

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12 December 2020

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

1 reference

12 December 2020

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation

1 reference

12 December 2020

Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred

1 reference

12 December 2020

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

1 reference

12 December 2020

A novel ATP1A2 mutation in a family with FHM type II

1 reference

12 December 2020

An investigation of the 5-HT2C receptor gene as a migraine candidate gene.

1 reference

12 December 2020

Association of progesterone receptor with migraine-associated vertigo

1 reference

12 December 2020

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine

1 reference

12 December 2020

Sporadic hemiplegic migraine

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12 December 2020

Recent advances in understanding migraine mechanisms, molecules and therapeutics

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12 December 2020

Functional effects of Na+,K+-ATPase gene mutations linked to familial hemiplegic migraine

1 reference

12 December 2020

Replication study of the insulin receptor gene in migraine with aura

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12 December 2020

A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria

1 reference

12 December 2020

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

1 reference

12 December 2020

Epidemiology of headache in Europe

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12 December 2020

No association of migraine to the GABA-A receptor complex on chromosome 15

1 reference

12 December 2020

Shared rearing environment in migraine: results from twins reared apart and twins reared together

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12 December 2020

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

1 reference

12 December 2020

The global burden of disease study: implications for neurology

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12 December 2020

Biomarkers in migraine: their promise, problems, and practical applications.

1 reference

12 December 2020

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus

1 reference

12 December 2020

Migraine in twins raised together and apart

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12 December 2020

Significant linkage to migraine with aura on chromosome 11q24.

1 reference

12 December 2020

Suppression of cortical spreading depression in migraine prophylaxis

1 reference

12 December 2020

Association of the C677T Polymorphism in the MTHFR Gene with Migraine: A Meta-Analysis

1 reference

12 December 2020

Classical migraine: symptoms between visual aura and headache onset

1 reference

12 December 2020

A gene for a new monogenic neurovascular migraine syndrome: a next step in unravelling molecular pathways for migraine?

1 reference

12 December 2020

Familial risk of migraine: A population-based study

1 reference

12 December 2020

MTHFR T677 homozygosis influences the presence of aura in migraineurs

1 reference

12 December 2020

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine

1 reference

12 December 2020

Migraine prevalence. A review of population-based studies.

1 reference

12 December 2020

ATP1A2 mutations in 11 families with familial hemiplegic migraine

1 reference

12 December 2020

Migraine and tumour necrosis factor gene polymorphism. An association study in a Sardinian sample

1 reference

12 December 2020

The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells

1 reference

12 December 2020

Sodium channel mutations in epilepsy and other neurological disorders

1 reference

12 December 2020

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

1 reference

12 December 2020

Consistently replicating locus linked to migraine on 10q22-q23

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12 December 2020

Investigation of hormone receptor genes in migraine.

1 reference

12 December 2020

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine

1 reference

12 December 2020

The International Classification of Headache Disorders: 2nd edition

1 reference

12 December 2020

A review of the genetic relation between migraine and epilepsy

1 reference

12 December 2020

Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.

1 reference

12 December 2020

Dopamine and migraine: biology and clinical implications

1 reference

12 December 2020

Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2

1 reference

12 December 2020

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

1 reference

12 December 2020

The mode of action of migraine triggers: a hypothesis.

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12 December 2020

SCN1A mutations and epilepsy

1 reference

12 December 2020

Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura

1 reference

12 December 2020

Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation

1 reference

12 December 2020

Migraine, aura, and cortical spreading depression: why are we still talking about it?

1 reference

12 December 2020

Genetic and environmental influences on migraine: a twin study across six countries

1 reference

12 December 2020

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

1 reference

12 December 2020

MTHFR C677T polymorphism and migraine with aura

1 reference

12 December 2020

Decreased number and function of endothelial progenitor cells in patients with migraine.

1 reference

12 December 2020

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

1 reference

12 December 2020

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine

1 reference

12 December 2020

Investigation of gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility

1 reference

12 December 2020

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

1 reference

12 December 2020

Familial migraine with and without aura: clinical characteristics and co-occurrence

1 reference

12 December 2020

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

1 reference

12 December 2020

Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes

1 reference

12 December 2020

Migraine without aura: A population-based twin study

1 reference

12 December 2020

Pathophysiology of the migraine aura. The spreading depression theory

1 reference

12 December 2020

Divergent sodium channel defects in familial hemiplegic migraine

1 reference

12 December 2020

A locus for migraine without aura maps on chromosome 14q21.2-q22.3.

1 reference

12 December 2020

Migraine: gene mutations and functional consequences

1 reference

12 December 2020

The association between headache and Val158Met polymorphism in the catechol-O-methyltransferase gene: the HUNT Study

1 reference

12 December 2020

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine

1 reference

12 December 2020

The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups

1 reference

12 December 2020

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1.

1 reference

12 December 2020

Familial typical migraine: significant linkage and localization of a gene to Xq24-28.

1 reference

12 December 2020

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation

1 reference

12 December 2020

Degeneration of the amygdala/piriform cortex and enhanced fear/anxiety behaviors in sodium pump alpha2 subunit (Atp1a2)-deficient mice

1 reference

12 December 2020

Elicited repetitive daily blindness: a new familial disorder related to migraine and epilepsy

1 reference

12 December 2020

Mechanisms of migraine aura revealed by functional MRI in human visual cortex

1 reference

12 December 2020

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities

1 reference

12 December 2020

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

1 reference

12 December 2020

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma

1 reference

12 December 2020

Migraine and MTHFR C677T genotype in a population-based sample

1 reference

12 December 2020

Genetic association study and meta-analysis of the HTR2C Cys23Ser polymorphism and migraine

1 reference

12 December 2020

Familial hemiplegic migraine

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12 December 2020

A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genes

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12 December 2020

Altered arterial function in migraine of recent onset

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12 December 2020

Thymidylate synthase promoter tandem repeat and MTHFD1 R653Q polymorphisms modulate the risk for migraine conferred by the MTHFR T677 allele

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12 December 2020

A typical migraine susceptibility region localizes to chromosome 1q31

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12 December 2020

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

1 reference

12 December 2020

Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects

1 reference

12 December 2020

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation

1 reference

12 December 2020

Migraine prophylactic drugs: proof of efficacy, utilization and cost

1 reference

12 December 2020

Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2

1 reference

12 December 2020

A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine

1 reference

12 December 2020

Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura

1 reference

12 December 2020

New genetic evidence for involvement of the dopamine system in migraine with aura

1 reference

12 December 2020

Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel

1 reference

12 December 2020

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

1 reference

12 December 2020

Genetics of migraine: an update with special attention to genetic comorbidity

1 reference

12 December 2020

Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2

1 reference

12 December 2020

Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with aura

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12 December 2020

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

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12 December 2020

Is stress a trigger factor for migraine?

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12 December 2020

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

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12 December 2020

Lack of association of endothelial nitric oxide synthase polymorphisms and migraine.

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12 December 2020

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy

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12 December 2020

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

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12 December 2020

Familial basilar migraine associated with a new mutation in the ATP1A2 gene

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12 December 2020

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

1 reference

12 December 2020

The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine

1 reference

12 December 2020

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

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12 December 2020

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

1 reference

12 December 2020

A susceptibility locus for migraine with aura, on chromosome 4q24.

1 reference

12 December 2020

Note on a possible correspondence between the scotomas of migraine and spreading depression of Leão

1 reference

12 December 2020

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

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12 December 2020

Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine

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12 December 2020

The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation

1 reference

12 December 2020

Migraine without aura and migraine with aura are distinct clinical entities: a study of four hundred and eighty-four male and female migraineurs from the general population

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12 December 2020

Migraine--current understanding and treatment

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12 December 2020

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons

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12 December 2020

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

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12 December 2020

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia.

1 reference

12 December 2020

Interrelationships among the MTHFR 677C>T polymorphism, migraine, and cardiovascular disease

1 reference

12 December 2020

Improved Description of the Migraine Aura by a Diagnostic Aura Diary

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12 December 2020

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine

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12 December 2020

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

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12 December 2020

The primary headaches: genetics, epigenetics and a behavioural genetic model

1 reference

12 December 2020

Migraine without aura and migraine with aura are distinct disorders. A population-based twin survey.

1 reference

12 December 2020

A high-density association screen of 155 ion transport genes for involvement with common migraine

1 reference

12 December 2020

Trait components provide tools to dissect the genetic susceptibility of migraine

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12 December 2020

Environmental epigenomics and disease susceptibility

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12 December 2020

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

1 reference

12 December 2020

The genetics of migraine without aura and migraine with aura

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12 December 2020

Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation

1 reference

12 December 2020

Angiotensin-converting enzyme gene insertion/deletion polymorphism in migraine patients

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12 December 2020

Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locus

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12 December 2020

No mutations in CACNA1A and ATP1A2 in probands with common types of migraine

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12 December 2020

10.1007/S00439-009-0684-Z

Identifiers

DOI

1 reference

Dimensions Publication ID

5 August 2017

1020463941

0 references

1 reference