Add to ORKGSickle cell anemia (SCA) is an autosomal recessive chronic hemolytic anemia, caused by homozygosity for the HBB:c.20A>T mutation. The disease presents with high clinical heterogeneity, stroke being the most devastating manifestation. This study aimed to identify genetic modulators of severe hemolysis and stroke risk in children with SCA, as well as understand their consequences at the hemorheological level. Sixty-six children with SCA were categorised according to their degree of cerebral vasculopathy (Stroke/Risk/Control). Relevant data were collected from patients’ medical records. Several polymorphic regions in genes related to vascular cell adhesion and tonus were characterized by molecular methodologies. Data analyses were performed u...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...
Sickle cell anemia (SCA) is a multifactorial-like monogenic disease that results from homozygosity f...
Sickle cell anemia (SCA) is an autosomal recessive chronic hemolytic anemia, caused by homozygosity ...
Sickle cell anemia (SCA) is an autosomal recessive chronic hemolytic anemia, caused by homozygosity ...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell disease (SCD) is a genetic disorder with recessive transmission, caused by the mutation ...
Sickle cell anaemia (SCA) is an autosomal recessive genetic disease that leads to the synthesis of h...
Sickle cell anaemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene. Howeve...
Palestras de difusão da cultura científica dirigidas aos colaboradores internos do INSA, podendo inc...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...
Sickle cell anemia (SCA) is a multifactorial-like monogenic disease that results from homozygosity f...
Sickle cell anemia (SCA) is an autosomal recessive chronic hemolytic anemia, caused by homozygosity ...
Sickle cell anemia (SCA) is an autosomal recessive chronic hemolytic anemia, caused by homozygosity ...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle cell anemia (SCA) is an autosomal recessive disease caused by the HBB:c.20A>T mutation that l...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell disease (SCD) is a genetic disorder with recessive transmission, caused by the mutation ...
Sickle cell anaemia (SCA) is an autosomal recessive genetic disease that leads to the synthesis of h...
Sickle cell anaemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene. Howeve...
Palestras de difusão da cultura científica dirigidas aos colaboradores internos do INSA, podendo inc...
Sickle cell anemia (SCA) is an autosomal recessive disease, caused by the mutation HBB:c.20A>T, orig...
Sickle cell anemia (SCA) arises from homozygosity for the mutation c.20A>T in the HBB gene which ori...
Sickle Cell Disease (SCD) is a clinically heterogeneous monogenic chronic anaemia characterized by s...
Sickle cell anemia (SCA) is a multifactorial-like monogenic disease that results from homozygosity f...