The clinical phenotype modulation of haemophilia by prothrombic gene mutations [2]

Haemophilia

Volumn 9, Issue 2, 2003, Pages 235-236

  Ferreira Araújo, Fernando Manuel ^a   Fraga, M ^a   Henriques, I ^a   Monteiro, F ^a   Meireles, E ^a   Pereira, C ^a   Lacerda, P ^a   Cunha Ribeiro, L M ^a  

^a HOSPITAL DE SÃO JOÃO   (Portugal)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; BLOOD CLOTTING FACTOR CONCENTRATE; PROCOAGULANT;

CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE SEVERITY; GENE LOCUS; GENE MUTATION; GENETIC DISORDER; HEMOPHILIA; HETEROZYGOTE; HUMAN; LETTER; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; RISK FACTOR; THROMBOSIS;

EID: 0037367463     PISSN: 13518216     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2516.2003.00718_2.x     Document Type: Letter

References (4)

1. Ettingshausen CE, Halimeh S, Kurnik K et al. Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors. Thromb Haemost 2001; 85: 218-20.
2. Vianello F, Belvini D, Dal Bello F et al. Mild bleeding diathesis in a boy with combined severe haemophilia B (C10400-T) and heterozygous factor V Leiden. Haemophilia 2001; 7: 511-4.
3. Lee DH, Walker IR, Teitel J et al. Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A. Thromb Haemost 2000; 83: 387-91.
4. Pruthi RK, Heit JÁ, Green MM et al. Venous thromboembolism after hip fracture surgery in a patient with haemophilia B and factor V Arg506Gln (factor V Leiden). Haemophilia 2000; 6: 631-4.