(Q35759348)

10 August 2017

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title

Toward a molecular genetic classification of familial hemiplegic migraine (English)

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10 August 2017

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Arn van den Maagdenberg

3

object named as

Arn M J M van den Maagdenberg

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Gisela M Terwindt

5

object named as

Gisela M Terwindt

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10 August 2017

7

Michel D Ferrari

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10 August 2017

6

Rune R Frants

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10 August 2017

Joost Haan

1

1 reference

10 August 2017

Esther E Kors

2

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10 August 2017

Kaate R J Vanmolkot

4

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10 August 2017

language of work or name

English

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publication date

1 June 2004

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Current Pain and Headache Reports

10 August 2017

published in

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10 August 2017

volume

8

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10 August 2017

issue

3

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10 August 2017

page(s)

238-243

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

10 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS11916-004-0058-0

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11916-004-0058-0

A new locus for hemiplegic migraine maps to chromosome 1q31

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11916-004-0058-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11916-004-0058-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11916-004-0058-0

A gene for familial hemiplegic migraine maps to chromosome 19

21 January 2018

1 reference

12 December 2020

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

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

Genetic heterogeneity of familial hemiplegic migraine

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic epidemiology of migraine and cluster headache

1 reference

12 December 2020

Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene

1 reference

12 December 2020

The genetics of migraine: implication for treatment approaches.

1 reference

12 December 2020

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

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

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

1 reference

12 December 2020

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family

1 reference

12 December 2020

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia

1 reference

12 December 2020

Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia

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

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

1 reference

12 December 2020

Physical mapping and characterization of the human Na,K-ATPase isoform, ATP1A4

1 reference

12 December 2020

A typical migraine susceptibility region localizes to chromosome 1q31

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

Is familial hemiplegic migraine a hereditary form of basilar migraine?

1 reference

12 December 2020

Increased risk of migraine with typical aura in probands with familial hemiplegic migraine and their relatives

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

Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome

1 reference

12 December 2020

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family

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

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

12 December 2020

Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Headache Classification Committee of the International Headache Society

1 reference

12 December 2020

Genetic heterogeneity of familial hemiplegic migraine

1 reference

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

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

1 reference

12 December 2020

10.1007/S11916-004-0058-0

Identifiers

DOI

1 reference

10 August 2017

1 reference