Prothrombotic polymorphisms in patients with Raynaud's phenomenon and migraine

Acta Physiologica Hungarica

Volumn 99, Issue 4, 2012, Pages 430-435

  Takats A ^a   Shemirani, Amir Houshang ^b   Zsori K S ^b   Andras C ^b   Csiki, Z ^b  

^a SEMMELWEIS UNIVERSITY   (Hungary)

^b UNIVERSITY OF DEBRECEN   (Hungary)

Author keywords

FVLeiden; FXIII A V34L; methyltetrahydrofolate reductase C677T; migraine; polymorphism; prothrombin G20210A; Raynaud's phenomenon

Indexed keywords

PROTHROMBIN;

ADULT; AGED; ALLELE; ARTICLE; CONTROLLED STUDY; DISEASE DURATION; FEMALE; FVLEIDEN GENE; FXIII A GENE; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC TRAIT; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; HUNGARY; MAJOR CLINICAL STUDY; MALE; METHYLTETRAHYDROFOLATE REDUCTASE GENE; MIGRAINE; PREVALENCE; PROTHROMBIN GENE; RAYNAUD PHENOMENON; RISK FACTOR; THROMBOSIS;

ADULT; FACTOR V; FACTOR XIII; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MIDDLE AGED; MIGRAINE DISORDERS; POLYMORPHISM, GENETIC; PREVALENCE; PROTHROMBIN; RAYNAUD DISEASE; RISK FACTORS; THROMBOSIS;

EID: 84871271644     PISSN: 0231424X     EISSN: 15882683     Source Type: Journal    
DOI: 10.1556/APhysiol.99.2012.4.7     Document Type: Article

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