Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine (Q28202137)

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scientific article (publication date: June 2001)

Language	Label	Description	Also known as
English	Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine	scientific article (publication date: June 2001)

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scholarly article

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Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine (English)

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based on heuristic

inferred from title

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based on heuristic

inferred from title

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based on heuristic

inferred from title

familial hemiplegic migraine

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based on heuristic

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11

object named as

M D Ferrari

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author name string

E E Kors

1

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G M Terwindt

2

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F L Vermeulen

3

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R B Fitzsimons

4

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P E Jardine

5

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P Heywood

6

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S Love

7

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A M van den Maagdenberg

8

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J Haan

9

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R R Frants

10

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language of work or name

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publication date

June 2001

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Annals of Neurology

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49

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6

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753-60

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Second impact syndrome

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Delayed deterioration following mild head injury in children

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https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

John Graham Senior Clinicians Award Lecture. Posttraumatic migraine

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Flunarizine in prophylaxis of childhood migraine. A double-blind, placebo-controlled, crossover study

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Is familial hemiplegic migraine a hereditary form of basilar migraine?

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

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/10.1002%2FANA.1031

21 January 2018

Structure and function of neuronal Ca2+ channels and their role in neurotransmitter release

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Control of glutamate release by calcium channels and kappa-opioid receptors in rodent and primate striatum

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Ontogenetic aspects of traumatic brain edema--facts and suggestions

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Pathophysiology of the migraine aura. The spreading depression theory

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Recent advances in the molecular understanding of voltage-gated Ca2+ channels.

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Familial periodic cerebellar ataxia: a problem of cerebellar intracellular pH homeostasis

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Respiratory arrest in familial hemiplegic migraine: a clinical and neuropathological study

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

A clinical, genetic, neuropathological study in a Japanese family with SCA 6 and a review of Japanese autopsy cases of autosomal dominant cortical cerebellar atrophy

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

21 January 2018

Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6).

1 reference

https://api.crossref.org/works/10.1002%2FANA.1031

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/10.1002%2FANA.1031

21 January 2018

Identifiers

10.1002/ANA.1031

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Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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