OBJECTIVE: To look for any possible coexistence of CACNA1A, ATP1A2, and KCNN3 gene
mutations in migraine patients who had human platelet HPA-1a/1b polymorphism, which is …

Background Mutations inCACNA1A, encoding a neuronal calcium channel subunit,
andATP1A2, encoding a catalytic subunit of a sodium-potassium–ATPase, have been found …

Objectives To perform an exhaustive mutational screening of the CACNA1A and ATP1A2
genes in 18 HM patients. Methods Direct sequencing of PCR amplicons, Multiplex Ligation …

Migraine is a common disorder with a significant genetic component. Mutations in the
CACNA1A gene are found in hemiplegic migraine (HM). Basilar-type (BM), another subtype …

Background and aim Migraine is the most common neurological disorder, affecting
approximately 12% of the adult population worldwide, caused by both environmental and …

Objective To search for differences in prevalence of a CACNA1E variant between migraine
without aura, various phenotypes of migraine with aura, and healthy controls. Background …

Objective To study the position of hemiplegic migraine in the clinical spectrum of migraine
with aura and to reveal the importance of CACNA1A, ATP1A2 and SCN1A in the …

MATERIALS AND METHODS: The subjects were the patients of migraine, in the age range
of 18-80 years, diagnosed by a Neurologist, as per the diagnostic criteria of International …

The aim of this study was to investigate the involvement of the CACNA1A and ATP1A2 gene
in a population-based sample of sporadic hemiplegic migraine (SHM). Patients with SHM …

Epidemiological studies indicate that migraine with typical aura (MA) has a major genetic
component but the genes for MA have not been identified. However, the autosomal …