Sickle cell anemia is an inflammatory disease and is characterized by chronic hemolysis. We sought to evaluate the association of lactate dehydrogenase levels with specific clinical phenotypes and laboratory variables in patients with sickle cell anemia.The present cross-sectional study was conducted in Sickle Cell Centre of Yolo in Kinshasa, the Democratic Republic of Congo. Two hundred and eleven patients with Sickle Cell Anemia in steady state were recruited. Seventy-four participants with normal Hb (Hb-AA) were selected as a control group.The average rates of hemoglobin, hematocrit, and red blood cells tended to be significantly lower in subjects with Hb-SS (p<0.001). The average rates of white blood cells, platelets, reticulocytes and ...
AbstractObjectiveThis study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis ...
Objective: This study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis biomark...
BackgroundSickle cell anemia (SCA) is a monogenic hemoglobinopathy associated with severe acute and ...
Sickle cell anemia is an inflammatory disease and is characterized by chronic hemolysis. We sought t...
Sickle cell anemia is an inflammatory disease and is characterized by chronic hemolysis. We sought t...
Leg ulcer is a disabling complication in patients with sickle cell anemia (SCA) but the exact pathop...
Leg ulcer is a disabling complication in patients with sickle cell anemia (SCA) but the exact pathop...
International audienceDense, dehydrated red blood cells (DRBCs) are a characteristic feature of sick...
Despite not yet explored, the serum lactate dehydrogenase (LDH) level in hemoglobinopathy SC (HbSC) ...
International audienceLeg ulcer is a disabling complication in patients with sickle cell anemia (SCA...
Albuminuria is a marker of glomerular damage in Sickle Cell Disease (SCD). In this study, we sought ...
High HbF levels and F cells are correlated with reduced morbidity and mortality in sickle cell disea...
<p>**: significant correlation at the 0.01 level;</p><p>*: significant correlation at the 0.05 level...
Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present hig...
International audienceTo perform a precise evaluation of the hemolytic status of patients with sickl...
AbstractObjectiveThis study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis ...
Objective: This study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis biomark...
BackgroundSickle cell anemia (SCA) is a monogenic hemoglobinopathy associated with severe acute and ...
Sickle cell anemia is an inflammatory disease and is characterized by chronic hemolysis. We sought t...
Sickle cell anemia is an inflammatory disease and is characterized by chronic hemolysis. We sought t...
Leg ulcer is a disabling complication in patients with sickle cell anemia (SCA) but the exact pathop...
Leg ulcer is a disabling complication in patients with sickle cell anemia (SCA) but the exact pathop...
International audienceDense, dehydrated red blood cells (DRBCs) are a characteristic feature of sick...
Despite not yet explored, the serum lactate dehydrogenase (LDH) level in hemoglobinopathy SC (HbSC) ...
International audienceLeg ulcer is a disabling complication in patients with sickle cell anemia (SCA...
Albuminuria is a marker of glomerular damage in Sickle Cell Disease (SCD). In this study, we sought ...
High HbF levels and F cells are correlated with reduced morbidity and mortality in sickle cell disea...
<p>**: significant correlation at the 0.01 level;</p><p>*: significant correlation at the 0.05 level...
Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present hig...
International audienceTo perform a precise evaluation of the hemolytic status of patients with sickl...
AbstractObjectiveThis study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis ...
Objective: This study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis biomark...
BackgroundSickle cell anemia (SCA) is a monogenic hemoglobinopathy associated with severe acute and ...