G1691A factor v and G20210A FII mutations, acute ischemic stroke of unknown cause, and patent foramen ovale

Thrombosis Research

Volumn 130, Issue 5, 2012, Pages 720-724

  Favaretto, Elisabetta ^a   Sartori, Michelangelo ^a   Conti, Eleonora ^a   Legnani, Cristina ^a   Palareti, Gualtiero ^a  

^a UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

G20210A prothrombin; Patent foramen ovale; prothrombotic disorders; R506Q FV Leiden; stroke; young

Indexed keywords

BLOOD CLOTTING FACTOR 5; ESTROGEN; PROTHROMBIN; SODIUM CHLORIDE;

ADULT; ALLELE; ARTICLE; BRAIN ISCHEMIA; CAUCASIAN; CONTROLLED STUDY; DEEP VEIN THROMBOSIS; DOPPLER ECHOGRAPHY; FEMALE; GENE MUTATION; GENOTYPE; HEART RIGHT LEFT SHUNT; HUMAN; MAJOR CLINICAL STUDY; MALE; PATENT FORAMEN OVALE; PREVALENCE; PRIORITY JOURNAL; RISK FACTOR; THROMBOPHILIA; VEIN INSUFFICIENCY;

FACTOR V; FORAMEN OVALE, PATENT; HUMANS; MALE; MIDDLE AGED; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTHROMBIN; RISK FACTORS; STROKE;

EID: 84867576604     PISSN: 00493848     EISSN: 18792472     Source Type: Journal    
DOI: 10.1016/j.thromres.2012.07.020     Document Type: Article

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