(Q28264653)

9

Arn M J M van den Maagdenberg

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Bettina Lorenz-Depiereux

5

Bettina Lorenz-Depiereux

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Michael Pusch

Michael Pusch

10

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Michel Ferrari

7

Michel D Ferrari

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author name string

Tobias Freilinger

2

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Gertrud Eckstein

3

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Elena Babini

4

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Bettina Lorenz-Depiereux

5

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Saskia Biskup

6

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Jürgen Herzog

8

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Tim M Strom

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

11

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language of work or name

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366

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page(s)

371-7

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issue

9483

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Prevalence of migraine headache in the United States. Relation to age, income, race, and other sociodemographic factors

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

The genetics of migraine

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

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7 January 2021

Allegro, a new computer program for multipoint linkage analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Molecular mechanism for an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Mechanisms of sodium channel inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Diversity of mammalian voltage-gated sodium channels.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Structural parts involved in activation and inactivation of the sodium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Amino acid residues required for fast Na(+)-channel inactivation: charge neutralizations and deletions in the III-IV linker

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Distribution of voltage-gated sodium channel ?-subunit and ?-subunit mRNAs in human hippocampal formation, cortex, and cerebellum

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Neurobiology of migraine.

1 reference

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7 January 2021

Pathophysiology of the migraine aura. The spreading depression theory

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Magnetoencephalographic fields from patients with spontaneous and induced migraine aura.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Potassium and calcium concentrations in interstitial fluid of hippocampal formation during paroxysmal responses.

1 reference

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7 January 2021

Mechanism of spreading cortical depression.

1 reference

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7 January 2021

Compounds in brain extracts causing spreading depression of cerebral cortical activity and contraction of crustacean muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy.

1 reference

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7 January 2021

Molecular basis of an inherited epilepsy

1 reference

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7 January 2021

Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v)1.1 sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966786-4

7 January 2021

10.1016/S0140-6736(05)66786-4

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

640145

640145

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference