(Q40349224)

19 September 2017

title

Implications of clinical subtypes of migraine with aura (English)

1 reference

19 September 2017

1 reference

3

1 reference

19 September 2017

author name string

Malene Kirchmann Eriksen

series ordinal

1

1 reference

19 September 2017

Lise Lykke Thomsen

series ordinal

2

1 reference

19 September 2017

publication date

1 February 2006

1 reference

19 September 2017

1 reference

19 September 2017

volume

46

1 reference

19 September 2017

issue

2

1 reference

19 September 2017

page(s)

286-297

1 reference

Migraine without aura and migraine with aura are distinct clinical entities: a study of four hundred and eighty-four male and female migraineurs from the general population

19 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Familial occurrence of migraine without aura and migraine with aura.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Clinical characteristics of 362 patients with familial migraine with aura.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

An epidemiological survey of hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Symptomatic and nonsymptomatic headaches in a general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Epidemiology of headache in a general population--a prevalence study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.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.1526-4610.2006.00286.X

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/10.1111%2FJ.1526-4610.2006.00286.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.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.1526-4610.2006.00286.X

A susceptibility locus for migraine with aura, on chromosome 4q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.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.1526-4610.2006.00286.X

Genetic heterogeneity in Italian families with familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Is familial hemiplegic migraine a hereditary form of basilar migraine?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Genetic loading in familial migraine with aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Observations on prodromes of classic migraine in a headache clinic population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

Focal hyperemia followed by spreading oligemia and impaired activation of rcbf in classic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

New international classification of migraine with aura (ICHD-2) applied to 362 migraine patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2006.00286.X

10.1111/J.1526-4610.2006.00286.X

21 January 2018

Identifiers

DOI

1 reference

19 September 2017

1 reference