Sickle cell disease (SCD) is one of the most common inherited diseases in the world and the patients present notorious clinical heterogeneity. It is known that patients with SCD present activation of the blood coagulation and fibrinolytic systems, especially during vaso-occlusive crises, but also during the steady state of the disease. We determined if the presence of the factor V gene G1691A mutation (factor V Leiden), the prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism may be risk factors for vascular complications in individuals with SCD. We studied 53 patients with SCD (60% being women), 29 with SS (sickle cell anemia; 28 years, range: 13-52 years) and 24 with SC (sickle-hemoglobin C ...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...
The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the methylenetetrahydrofolate reduc...
Background: Sickle cell disease (SCD) is a Mendelian disease characterized by multigenic phenotypes....
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Vaso-occlusion is a determinant ...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
Introduction: Sickle cell disease (SCD) is an inflammatory condition with an increase in the adhesio...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
Sickle cell disease is an inflammatory condition with a pathophysiology that involves vaso-occlusive...
The C677T methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and the G20210A mutation at ...
Sickle cell disease (SCD) is a monogenetic disorder caused by a mutation in the [H9252]-globin gene ...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Transcranial Doppler ultrasonography measures cerebral blood flow velocity (CBFv) of basal intracran...
Background Polymorphisms of platelet membrane glycoproteins such as human platelet antigen (HPA)-1b,...
Dissertação de mestrado em Genética Molecular e Biomedicina apresentada à Faculdade de Ciências e Te...
We evaluated the relevance of plasma homocysteine (HC) and the TT genotype of the methylenetetrahydr...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...
The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the methylenetetrahydrofolate reduc...
Background: Sickle cell disease (SCD) is a Mendelian disease characterized by multigenic phenotypes....
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Vaso-occlusion is a determinant ...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
Introduction: Sickle cell disease (SCD) is an inflammatory condition with an increase in the adhesio...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
Sickle cell disease is an inflammatory condition with a pathophysiology that involves vaso-occlusive...
The C677T methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and the G20210A mutation at ...
Sickle cell disease (SCD) is a monogenetic disorder caused by a mutation in the [H9252]-globin gene ...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Transcranial Doppler ultrasonography measures cerebral blood flow velocity (CBFv) of basal intracran...
Background Polymorphisms of platelet membrane glycoproteins such as human platelet antigen (HPA)-1b,...
Dissertação de mestrado em Genética Molecular e Biomedicina apresentada à Faculdade de Ciências e Te...
We evaluated the relevance of plasma homocysteine (HC) and the TT genotype of the methylenetetrahydr...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...
The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the methylenetetrahydrofolate reduc...
Background: Sickle cell disease (SCD) is a Mendelian disease characterized by multigenic phenotypes....