Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Vaso-occlusion is a determinant for most signs and symptoms of sickle-cell anemia (SCA). The mechanisms involved in the pathogenesis of vascular complications in SCA remain unclear. It is known that genetic polymorphisms associated with thrombophilia may be potential modifiers of clinical features of SCA. The genetic polymorphisms C677T and A1298C relating to the enzyme methylenetetrahydrofolate reductase (MTHFR), a clotting Factor V Leiden mutation (1691G -> A substitution of Factor V Leiden), and the mutant prothrombin 20210A allele were analyzed in this study. The aim was to find possible correlations with vascular complications and thrombophilia markers in a group of SC...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
A trombose parece ter papel importante na fisiopatologia de algumas das manifestacoes clinicas obser...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Sickle cell disease (SCD) is one of the most common inherited diseases in the world and the patients...
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 ...
Embora a anemia falciforme (AF) resulte da homozigosidade de uma única mutação, no codon 6 do locus ...
Background Polymorphisms of platelet membrane glycoproteins such as human platelet antigen (HPA)-1b,...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
Dissertação de mestrado em Genética Molecular e Biomedicina apresentada à Faculdade de Ciências e Te...
21ª Reunião da Sociedade Portuguesa de Genética Humana, 16-18 nov 2017Sickle cell anemia (SCA) is an...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
Sickle-cell anaemia (SCA) is a clinically heterogeneous autosomal recessive monogenic chronic anaemi...
Introduction: Sickle cell disease (SCD) is an inflammatory condition with an increase in the adhesio...
Sickle cell disease (SCD) is characterized by a very heterogeneous clinical ranging from patients wh...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
A trombose parece ter papel importante na fisiopatologia de algumas das manifestacoes clinicas obser...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Sickle cell disease (SCD) is one of the most common inherited diseases in the world and the patients...
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 ...
Embora a anemia falciforme (AF) resulte da homozigosidade de uma única mutação, no codon 6 do locus ...
Background Polymorphisms of platelet membrane glycoproteins such as human platelet antigen (HPA)-1b,...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
Dissertação de mestrado em Genética Molecular e Biomedicina apresentada à Faculdade de Ciências e Te...
21ª Reunião da Sociedade Portuguesa de Genética Humana, 16-18 nov 2017Sickle cell anemia (SCA) is an...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
Sickle-cell anaemia (SCA) is a clinically heterogeneous autosomal recessive monogenic chronic anaemi...
Introduction: Sickle cell disease (SCD) is an inflammatory condition with an increase in the adhesio...
Sickle cell disease (SCD) is characterized by a very heterogeneous clinical ranging from patients wh...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
A trombose parece ter papel importante na fisiopatologia de algumas das manifestacoes clinicas obser...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...