(Q34657045)

3 August 2017

1 reference

title

Migraine and epilepsy: genetically linked? (English)

1 reference

3 August 2017

1 reference

Arn van den Maagdenberg

series ordinal

2

object named as

Arn M J M van den Maagdenberg

0 references

Michel Ferrari

series ordinal

4

object named as

Michel D Ferrari

1 reference

3 August 2017

Joost Haan

1

1 reference

3 August 2017

Oebele F Brouwer

series ordinal

3

1 reference

3 August 2017

publication date

1 September 2008

1 reference

Expert Review of Neurotherapeutics: a key contribution to decision making in the treatment of neurologic and neuropsychiatric disorders

3 August 2017

published in

1 reference

3 August 2017

volume

8

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3 August 2017

issue

9

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3 August 2017

page(s)

1307-1311

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Migraine with aura is a risk factor for unprovoked seizures in children

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Migraine: gene mutations and functional consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Monogenic idiopathic epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Chronic disorders with episodic manifestations: focus on epilepsy and migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Shortened cortical silent period in facial muscles of patients with migraine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Altered cortical visual processing in individuals with a spreading photoparoxysmal EEG response

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Genetic mechanisms that underlie epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Genetic models of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Intrinsic excitability, synaptic potentials, and short-term plasticity in human epileptic neocortex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Migraine and epilepsy: clinical and pathophysiological relations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Animal models of migraine: looking at the component parts of a complex disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca2+ channel alpha1A subunit gene and exhibits absence seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Antiepileptic drugs in migraine: from clinical aspects to cellular mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Suppression of cortical spreading depression in migraine prophylaxis

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

Non-conducting functions of voltage-gated ion channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

21 January 2018

From molecule to malady

1 reference

https://api.crossref.org/works/10.1586%2F14737175.8.9.1307

10.1586/14737175.8.9.1307

21 January 2018

Identifiers

DOI

1 reference

3 August 2017

1 reference