(Q44984439)

8 December 2017

title

Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes (English)

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Noèlia Fernàndez-Castillo

8 December 2017

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3

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8

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8 December 2017

E Cuenca-León

1

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8 December 2017

R Corominas

2

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8 December 2017

V Volpini

4

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8 December 2017

M Del Toro

5

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8 December 2017

M Roig

6

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8 December 2017

A Macaya

7

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8 December 2017

language of work or name

English

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publication date

17 July 2008

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8 December 2017

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8 December 2017

volume

28

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8 December 2017

issue

10

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8 December 2017

page(s)

1039-1047

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

8 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

Familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

BENIGN PAROXYSMAL VERTIGO OF CHILDHOOD. (A VARIETY OF VESTIBULAR NEURONITIS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

The impact of splice isoforms on voltage-gated calcium channel alpha1 subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

Genetic heterogeneity in Italian families with familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

ATP1A2 mutations in 11 families with familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

A novel ATP1A2 mutation in a family with FHM type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

SCN1A mutations and epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

Benign paroxysmal torticollis in infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

Evaluation of vestibular functions in children with vertigo attacks

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

The PSIPRED protein structure prediction server

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01645.X

10.1111/J.1468-2982.2008.01645.X

21 January 2018

Identifiers

DOI

1 reference

8 December 2017

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