Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine
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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature updateTwo de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraineMigraine genetics.Therapies in development for the treatment of migraine.Pseudomigraine with lymphocytic pleocytosis: a calcium channelopathy? Clinical description of 10 cases and genetic analysis of the familial hemiplegic migraine gene CACNA1A.The primary headaches: genetics, epigenetics and a behavioural genetic model.Genetic biomarkers for migraine.Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures.Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.Migraine genes and the relation to gender.Pearls and pitfalls in genetic studies of migraine.Pathophysiology of Migraine: A Disorder of Sensory Processing.Rare clinical findings in a patient with sporadic hemiplegic migraine: FDG-PET provides diminished brain metabolism at 10-year follow-up.Implications of clinical subtypes of migraine with aura.Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder.Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes.Sporadic hemiplegic migraine.Cerebellar Atrophy and Changes in Cytokines Associated with the CACNA1A R583Q Mutation in a Russian Familial Hemiplegic Migraine Type 1 Family.Familial and sporadic hemiplegic migraine: diagnosis and treatment.Intrinsic Disorder in Proteins with Pathogenic Repeat Expansions.Imaging abnormalities in sporadic hemiplegic migraine on conventional MRI, diffusion and perfusion MRI and MRS.Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes.Familial hemiplegic migraine: follow-up findings of diffusion-weighted magnetic resonance imaging (MRI), perfusion-MRI and [99mTc] HMPAO-SPECT in a patient with prolonged hemiplegic aura.A single-fibre EMG study of neuromuscular transmission in migraine patients.Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine PatientsFamilial Hemiplegic Migraine Type 1 Shows no Hypersensitivity to Nitric OxideHemiplegic Migraine: Clinical Features, Links with Basilar-type Migraine, Current and Future TreatmentAmino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine
P2860
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P2860
Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine
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2002 nî lūn-bûn
@nan
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
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2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@ast
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@en
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@nl
type
label
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@ast
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@en
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@nl
prefLabel
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@ast
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@en
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@nl
P2093
P1433
P1476
Mutation analysis of the CACNA ...... h sporadic hemiplegic migraine
@en
P2093
Arn Van den Maagdenberg
Esther Kors
Frans Vermeulen
Joost Haan
Rune Frants
P304
P356
10.1001/ARCHNEUR.59.6.1016
P407
P577
2002-06-01T00:00:00Z