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Volumn 83, Issue 11, 2004, Pages 712-715
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Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: Results of a single-center case-control study
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Author keywords
Egypt; Factor II mutation; Factor V Leiden; Hereditary thrombophilia; Portal vien thrombosis; Protein C deficiency; Prothrombin gene mutation
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Indexed keywords
ACTIVATED PROTEIN C;
ANTITHROMBIN III;
BLOOD CLOTTING FACTOR 5;
BLOOD CLOTTING FACTOR 5 LEIDEN;
PROTEIN C;
PROTEIN S;
PROTHROMBIN;
ACTIVATED PROTEIN C RESISTANCE;
ADOLESCENT;
AGE;
ANTICOAGULATION;
ANTITHROMBIN DEFICIENCY;
ARTICLE;
CASE CONTROL STUDY;
CHILD;
CLINICAL ARTICLE;
COMORBIDITY;
CONTROLLED STUDY;
EGYPT;
FEMALE;
GENE MUTATION;
GENETIC ANALYSIS;
HEREDITY;
HUMAN;
MALE;
MEDICAL ASSESSMENT;
NEWBORN SEPSIS;
PATHOGENESIS;
PORTAL HYPERTENSION;
PORTAL VEIN THROMBOSIS;
PREVALENCE;
PRIORITY JOURNAL;
PROTEIN C DEFICIENCY;
PROTEIN S DEFICIENCY;
RISK FACTOR;
SEX DIFFERENCE;
THROMBOPHILIA;
UMBILICAL ARTERY CATHETERIZATION;
ACTIVATED PROTEIN C RESISTANCE;
ADOLESCENT;
ANTITHROMBIN III;
BLOOD PROTEINS;
CASE-CONTROL STUDIES;
CHILD;
CHILD, PRESCHOOL;
EGYPT;
FACTOR V;
FEMALE;
HETEROZYGOTE;
HOSPITALS;
HUMANS;
INFANT;
MALE;
MUTATION;
PORTAL VEIN;
PROTEIN C;
PROTEIN S;
PROTHROMBIN;
THROMBOSIS;
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EID: 7444249002
PISSN: 09395555
EISSN: None
Source Type: Journal
DOI: 10.1007/s00277-004-0921-4 Document Type: Article |
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Times cited : (45)
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References (7)
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