Thrombosis-associated gene variants in sickle cell anemia

Thrombosis and Haemostasis

Volumn 87, Issue 2, 2002, Pages 356-358

  Romana, Marc ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

PROTHROMBIN;

ADULT; AFRICA; ALLELE; CHILD; CONTROLLED STUDY; EUROPE; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HIGH RISK POPULATION; HUMAN; LETTER; MAJOR CLINICAL STUDY; MORBIDITY; NEWBORN; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; RISK FACTOR; SICKLE CELL ANEMIA; THROMBOCYTE ACTIVATION; THROMBOPHILIA; THROMBOSIS;

EID: 0036172543     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1613007     Document Type: Letter

References (15)

1. Sickle cell disease
2. Pathogenesis and treatment of sickle cell disease
3. Disturbance of plasma and platelet thrombospondin levels in sickle cell disease
4. Vascular occlusion in sickle cell disease: Current concepts and unanswered questions
5. Pulmonary entrapment of sickle cells: The role of regional alveolar hypoxia
6. Evolution of laboratory parameters during sickle cell painful crisis: Evidence with dense cell sequestration without thrombosis
7. Prothrombotic changes in children with sickle cell disease: Relationships to cerebrovascular disease and transfusion
8. A common genetic variant in the 3′ - Untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
9. A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
10. High prevalence of a mutation in the cystathionine b synthase gene
11. Hemostatic risk factors and arterial thrombotic disease
12. Clinical events in the first decade in a cohort of infants with sickle cell disease
13. Prevalence, clinical features, and risk factors of osteonecrosis of the femoral head among adults with sickle cell disease
14. Homocysteine and thrombotic disease
15. A 68 bp insertion found in a homocystinuric patient is a common variant and is skipped by alternative splicing of the cystathionine b-synthase mRNA