Case report: Heterozygosity for factor V Leiden and G20210A prothrombin genotypes in a patient with mesenteric vein thrombosis

Digestive Diseases and Sciences

Volumn 47, Issue 3, 2002, Pages 601-606

  Al Juburi, Amar ^a   Scott, Margie A ^b   Shah, Hemendra R ^b   Raufman, Jean Pierre ^a  

^a UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^b CENTRAL ARKANSAS VETERANS HEALTHCARE SYSTEM   (United States)

Author keywords

Blood coagulation disorder; Factor V; Mesenteric vein; Methylenetetrahydrofolate reductase; Prothrombin G20210A; Thrombosis

Indexed keywords

ALANINE; ANTIBIOTIC AGENT; BLOOD CLOTTING FACTOR 5 LEIDEN; GLYCINE; HEPARIN; NARCOTIC AGENT; PROTHROMBIN; TISSUE PLASMINOGEN ACTIVATOR; WARFARIN; BLOOD CLOTTING FACTOR 5;

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC PROCEDURE; DISEASE COURSE; EPIGASTRIC PAIN; GENE MUTATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENOTYPE; HETEROZYGOSITY; HUMAN; INTESTINE NECROSIS; JEJUNUM DISEASE; MALE; MESENTERIC VEIN THROMBOSIS; PRIORITY JOURNAL; SUPERIOR MESENTERIC VEIN; TREATMENT OUTCOME; BLOOD; GENETIC VARIABILITY; GENETICS; JEJUNUM; MESENTERIC BLOOD VESSEL OCCLUSION; MESENTERIC VEIN; MUTATION; PEDIGREE; POINT MUTATION; THROMBOPHILIA; THROMBOSIS; VASCULARIZATION;

ADULT; FACTOR V; GENOTYPE; HUMANS; JEJUNUM; MALE; MESENTERIC VASCULAR OCCLUSION; MESENTERIC VEINS; MUTATION; PEDIGREE; POINT MUTATION; PROTHROMBIN; THROMBOPHILIA; THROMBOSIS; VARIATION (GENETICS);

EID: 0036118524     PISSN: 01632116     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1017928421966     Document Type: Article

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