(Q36995199)

17 August 2017

1 reference

title

Molecular mechanisms of migraine? (English)

1 reference

17 August 2017

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S V Ramagopalan

1

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PubMed ID

17987250

17 August 2017

N E Ramscar

series ordinal

2

1 reference

PubMed ID

17987250

17 August 2017

M Z Cader

series ordinal

3

1 reference

17 August 2017

7 November 2007

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17 August 2017

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17 August 2017

254

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17 August 2017

12

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17 August 2017

1629-1635

1 reference

https://scigraph.springernature.com/pub.10.1007/s00415-007-0641-5

17 August 2017

0 references

cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-007-0641-5

The place of migraine as a channelopathy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-007-0641-5

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

21 January 2018

1 reference

12 December 2020

Prevalence and burden of migraine in the United States: data from the American Migraine Study II.

1 reference

12 December 2020

Calcitonin gene-related peptide receptor antagonist BIBN 4096 BS for the acute treatment of migraine

1 reference

12 December 2020

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

12 December 2020

Brain stem activation in spontaneous human migraine attacks

1 reference

12 December 2020

Neurogenically mediated leakage of plasma protein occurs from blood vessels in dura mater but not brain

1 reference

12 December 2020

Genomewide significant linkage to migrainous headache on chromosome 5q21.

1 reference

12 December 2020

Neurogenic inflammation and migraine: implications for the therapeutics

1 reference

12 December 2020

Haplotype-based systematic association studies of ATP1A2 in migraine with aura

1 reference

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

Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmission

1 reference

12 December 2020

Nitric oxide metabolites, prostaglandins and trigeminal vasoactive peptides in internal jugular vein blood during spontaneous migraine attacks

1 reference

12 December 2020

International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels

1 reference

12 December 2020

Sporadic hemiplegic migraine

1 reference

12 December 2020

Sensitization of meningeal sensory neurons and the origin of headaches

1 reference

12 December 2020

Block of (Na+,K+)ATPase with ouabain induces spreading depression-like depolarization in hippocampal slices.

1 reference

12 December 2020

Magnetoencephalographic fields from patients with spontaneous and induced migraine aura.

1 reference

12 December 2020

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

1 reference

12 December 2020

Cortical spreading depression in migraine

1 reference

12 December 2020

The neurobiology of vascular head pain

1 reference

12 December 2020

Significant linkage to migraine with aura on chromosome 11q24.

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

Familial hemiplegic migraine: a ion channel disorder

1 reference

12 December 2020

Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha1A subunit of P/Q type calcium channels

1 reference

12 December 2020

The International Classification of Headache Disorders: 2nd edition

1 reference

12 December 2020

Symptomatic migraine and sensitization of trigeminal nociception associated with contralateral pontine cavernoma

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 genetic spectrum of a population-based sample of familial hemiplegic migraine.

1 reference

12 December 2020

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

1 reference

12 December 2020

MTHFR C677T polymorphism and migraine with aura

1 reference

12 December 2020

Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13

1 reference

12 December 2020

Neurobiology of migraine.

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

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

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

Epidemiology of headache

1 reference

12 December 2020

Update on the genetics of migraine

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Migraine and MTHFR C677T genotype in a population-based sample

1 reference

12 December 2020

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

1 reference

12 December 2020

A typical migraine susceptibility region localizes to chromosome 1q31

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

Migraine with aura: new understanding from clinical epidemiologic studies

1 reference

12 December 2020

Gating deficiency in a familial hemiplegic migraine type 1 mutant P/Q-type calcium channel

1 reference

12 December 2020

Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG

1 reference

12 December 2020

The periaqueductal grey matter modulates trigeminovascular input: a role in migraine?

1 reference

12 December 2020

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

1 reference

12 December 2020

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

1 reference

12 December 2020

The pharmacology of headache

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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

1 reference

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

1 reference

12 December 2020

Familial hemiplegic migraine, nystagmus, and cerebellar atrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

Retinal plasma extravasation in animals but not in humans: implications for the pathophysiology of migraine.

1 reference

12 December 2020

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

1 reference

12 December 2020

Trait components provide tools to dissect the genetic susceptibility of migraine

1 reference

12 December 2020

International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels

1 reference

12 December 2020

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics

1 reference

12 December 2020

A PET study exploring the laterality of brainstem activation in migraine using glyceryl trinitrate

1 reference

12 December 2020

10.1007/S00415-007-0641-5

Identifiers

DOI

1 reference

17 August 2017

1 reference

PubMed ID

17987250