(Q40104204)

English

Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation

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scholarly article

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Europe PubMed Central

PubMed publication ID

17 September 2017

Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

1 reference

based on heuristic

inferred from title

familial hemiplegic migraine

1 reference

based on heuristic

inferred from title

7

object named as

M D Ferrari

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

author name string

N Pelzer

1

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Europe PubMed Central

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17 September 2017

D E Blom

2

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Europe PubMed Central

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17 September 2017

A H Stam

3

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

L S Vijfhuizen

4

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

Atm Hageman

5

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

J A van Vliet

6

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

Amjm van den Maagdenberg

8

1 reference

Europe PubMed Central

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17 September 2017

J Haan

9

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Europe PubMed Central

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17 September 2017

G M Terwindt

10

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17 September 2017

language of work or name

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publication date

24 May 2016

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Europe PubMed Central

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17 September 2017

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Europe PubMed Central

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17 September 2017

37

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Europe PubMed Central

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17 September 2017

8

1 reference

Europe PubMed Central

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17 September 2017

737-755

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

Molecular genetics of migraine

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Migraine and restless legs syndrome in men.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Validation of the International Restless Legs Syndrome Study Group rating scale for restless legs syndrome

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

A novel ATP1A2 mutation in a family with FHM type II

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Prolonged hemiplegic episodes in children due to mutations in ATP1A2.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Multimodal neuroimaging in a child with sporadic hemiplegic migraine: a contribution to understanding pathogenesis

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

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

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Role of excitatory amino acid-mediated ionic fluxes in traumatic brain injury

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Migraine pathophysiology: lessons from mouse models and human genetics

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

The postictal state: effects of age and underlying brain dysfunction

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Definition of the postictal state: when does it start and end?

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Spreading convulsions, spreading depolarization and epileptogenesis in human cerebral cortex

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis. A report of 50 cases.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Pseudomigraine with lymphocytic pleocytosis: a calcium channelopathy? Clinical description of 10 cases and genetic analysis of the familial hemiplegic migraine gene CACNA1A.

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Acute confusional migraine: is it a distinct form of migraine?

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Recurrent Episodes of Coma: An Unusual Phenotype of Familial Hemiplegic Migraine with Linkage to Chromosome 1

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1177%2F0333102416651284

21 January 2018

Identifiers

10.1177/0333102416651284

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 September 2017

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