Thrombophilia in thalassemia major patients: Analysis of genetic predisposing factors

Haematologica

Volumn 86, Issue 10, 2001, Pages 1112-1113

  Iolascon, A ^a   Giordano, P ^a   Storelli, S ^a   Li, H H ^a   Coppola, B ^a   Piga, A ^a   Fantola, E ^a   Forni, G ^a   Cianciulli, P ^a   Perrotta, S ^a   Magnano, C ^a   Maggio, A ^a   Mangiagli, A ^a   Devoto, M ^a  

^a UNIVERSITY OF FOGGIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN; METHYLENETETRAHYDROFOLATE DEHYDROGENASE; PROTHROMBIN;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CLINICAL ARTICLE; DATA ANALYSIS; FEMALE; GENETIC MARKER; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; HEMOSTASIS; HUMAN; HYPERCOAGULABILITY; MALE; PREVALENCE; RETROSPECTIVE STUDY; THALASSEMIA MAJOR; THROMBOCYTE AGGREGATION; THROMBOPHILIA; URINARY EXCRETION;

ADOLESCENT; ADULT; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; RETROSPECTIVE STUDIES; RISK FACTORS; THALASSEMIA; THROMBOPHILIA;

EID: 0034756542     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

1. Thromboembolic complications in β thalassemia major
2. Survival and causes of death in thalassaemia major
3. A chronic hypercoagulable state in patients with β thalassaemia major is already present in childood
4. Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia
5. Resistance to activated protein C in thalassaemic patients: An underlying cause of thrombosis
6. Mutation in blood coagulation factor V associated with resistance to activated protein C
7. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
8. A candidate genetic risk factor for vascular disease: A common mutation in a methylenetetrahydrofalate reductase
9. A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis
10. A polymorphism in the 5′ region of coagulation factor VII gene (F7) caused by an inserted decanucleotide
11. Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction
12. Pulmonary thromboembolism in thalassemia intermedia patients