Background Polymorphisms of platelet membrane glycoproteins such as human platelet antigen (HPA)-1b, HPA-2b, the -5T/C Kozak sequence and C807T have been described as risk factors for vascular disease. Vaso-occlusion episodes are a common feature of sickle cell anaemia (SCA), leading to complications such as stroke, acute chest syndrome, avascular head femur necrosis and priapism. Complex interactions are involved in vaso-occlusion, and activated platelets may play an important role. These data raised the question of whether platelet polymorphisms could be implicated in occlusive vascular complications (OVC) of SCA.Materials and Methods in this study, 97 patients with SCA were analysed in two groups: 34 patients presenting with OVC (SCA-VC)...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell anemia (SCA) is an autosomal recessive chronic hemolytic anemia, caused by homozygosity ...
Introduction: Sickle cell anaemia (SCA) is a clinically heterogeneous autosomal recessive monogenic ...
Background Polymorphisms of platelet membrane glycoproteins such as human platelet antigen (HPA)-1b,...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Vaso-occlusion is a determinant ...
Platelets are pivotal to the process of arterial thrombosis resulting in ischemic stroke. Occlusive ...
Introduction: Sickle cell disease (SCD) is an inflammatory condition with an increase in the adhesio...
AbstractOBJECTIVESWe sought to determine the role of the −5T/C polymorphism of the platelet glycopro...
Texto completo: acesso restrito. p. 107–116Platelet membrane glycoprotein (GP) Ibα is a critical co...
Sickle cell disease is an inflammatory condition with a pathophysiology that involves vaso-occlusive...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Platelet membrane glycoprotein (GP) Ibalpha is a critical component of platelet adhesion complex to ...
Background: Sickle cell disease (SCD) is a Mendelian disease characterized by multigenic phenotypes....
Background: Glanzmann Thrombasthenia (GT) is a rare autosomal disease. HPA (Human Platelet Alloantig...
Some mutations in the Factor V (FV) gene cause a hypercoagulable state, primarily through resistance...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell anemia (SCA) is an autosomal recessive chronic hemolytic anemia, caused by homozygosity ...
Introduction: Sickle cell anaemia (SCA) is a clinically heterogeneous autosomal recessive monogenic ...
Background Polymorphisms of platelet membrane glycoproteins such as human platelet antigen (HPA)-1b,...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Vaso-occlusion is a determinant ...
Platelets are pivotal to the process of arterial thrombosis resulting in ischemic stroke. Occlusive ...
Introduction: Sickle cell disease (SCD) is an inflammatory condition with an increase in the adhesio...
AbstractOBJECTIVESWe sought to determine the role of the −5T/C polymorphism of the platelet glycopro...
Texto completo: acesso restrito. p. 107–116Platelet membrane glycoprotein (GP) Ibα is a critical co...
Sickle cell disease is an inflammatory condition with a pathophysiology that involves vaso-occlusive...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Platelet membrane glycoprotein (GP) Ibalpha is a critical component of platelet adhesion complex to ...
Background: Sickle cell disease (SCD) is a Mendelian disease characterized by multigenic phenotypes....
Background: Glanzmann Thrombasthenia (GT) is a rare autosomal disease. HPA (Human Platelet Alloantig...
Some mutations in the Factor V (FV) gene cause a hypercoagulable state, primarily through resistance...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell anemia (SCA) is an autosomal recessive chronic hemolytic anemia, caused by homozygosity ...
Introduction: Sickle cell anaemia (SCA) is a clinically heterogeneous autosomal recessive monogenic ...