Factor XIII Val34Leu is a genetic factor involved in the aetiology of venous thrombosisFRANCO, R. F; REITSMA, P. H; LOURENCO, D et al.Thrombosis and haemostasis. 1999, Vol 81, Num 5, pp 676-679, issn 0340-6245Article

The 20210 G→ A mutation in the 3'-untranslated region of the prothrombin gene and the risk for arterial thrombotic diseaseFRANCO, R. F; TRIP, M. D; TEN CATE, H et al.British journal of haematology. 1999, Vol 104, Num 1, pp 50-54, issn 0007-1048Article

Are haemochromatosis mutations related to the severity of liver disease in hepatitis C virus infection?MARTINELLI, A. L. C; FRANCO, R. F; VILLANOVA, M. G et al.Acta haematologica. 1999, Vol 102, Num 3, pp 152-156, issn 0001-5792Article

Heterogeneous ethnic distribution of the 844ins68 in the cystathionine β-synthase geneFRANCO, R. F; ELION, J; LAVINHA, J et al.Human heredity. 1998, Vol 48, Num 6, pp 338-342, issn 0001-5652Article

Analysis of the 677 C→T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groupsFRANCO, R. F; ARAUJO, A. G; GUERREIRO, J. F et al.Thrombosis and haemostasis. 1998, Vol 79, Num 1, pp 119-121, issn 0340-6245Article

Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular diseaseFRANCO, R. F; ZAGO, M. A; TRIP, M. D et al.British journal of haematology. 1998, Vol 102, Num 5, pp 1172-1175, issn 0007-1048Article

The in vivo kinetics of tissue factor messenger RNA expression during human endotoxemia : Relationship with activation of coagulationFRANCO, R. F; DE JONGE, E; VAN DER POLL, T et al.Blood. 2000, Vol 96, Num 2, pp 554-559, issn 0006-4971Article

Factor XIII Val34Leu and the risk of myocardial infarctionFRANCO, R. F; PAZIN-FILHO, A; TAVELLA, M. H et al.Haematologica (Roma). 2000, Vol 85, Num 1, pp 67-71, issn 0390-6078Article

Factor V Leiden and factor II G20210A mutations in patients with recurrent abortionSOUZA, S. S; FERRIANI, R. A; PONTES, A. G et al.Human reproduction (Oxford. Print). 1999, Vol 14, Num 10, pp 2448-2450, issn 0268-1161Article

Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patientsMORELLI, V. M; LOURENCO, D. M; D'ALMEIDA, V et al.Blood coagulation & fibrinolysis. 2002, Vol 13, Num 3, pp 271-275, issn 0957-5235Article

A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic diseaseFRANCO, R. F; MORELLI, V; LOURENCO, D et al.British journal of haematology. 1999, Vol 105, Num 2, pp 556-559, issn 0007-1048Article

Prevalence of the G20210A polymorphism in the 3'-untranslated region of the prothrombin gene in different human populationsFRANCO, R. F; SANTOS, S. E. B; ELION, J et al.Acta haematologica. 1998, Vol 100, Num 1, pp 9-12, issn 0001-5792Article

Factor V Arg³⁰⁶→ Thr (factor V Cambridge) and factor V Arg³⁰⁶→ Gly mutations in venous thrombotic diseaseFRANCO, R. F; MAFFEI, F. H; LOURENCO, D et al.British journal of haematology. 1998, Vol 103, Num 3, pp 888-890, issn 0007-1048Article

Racial heterogeneity of DNA polymorphisms linked to the A and the O alleles of the ABO blood group geneZAGO, M. A; TAVELLA, M. H; SIMOES, B. P et al.Annals of human genetics. 1996, Vol 60, pp 67-72, issn 0003-4800, 1Article

Relative frequencies of the two O alleles of the histo-blood ABH system in different racial groupsFRANCO, R. F; SIMOES, B. P; ZAGO, M. A et al.Vox sanguinis (Basel. 1956). 1995, Vol 69, Num 1, pp 50-52, issn 0042-9007Article

Molecular bases of the ABO blood groups of Indians from the Brazilian Amazon RegionFRANCO, R. F; SIMOES, B. P; GUERREIRO, J. F et al.Vox sanguinis (Basel. 1956). 1994, Vol 67, Num 3, pp 299-301, issn 0042-9007Article