Background: Sickle cell anemia (SCD) is one of many haemoglobinopathic disorders which is probably the most common known hereditary blood disorder. In this disease, the homozygous state in which the sickle gene is inherited from the father and the mother, and patients with sickle cell disorders often suffer from chronic hemolytic anemia, which causes bone marrow hyperplasia too. The present study was designed to evaluate the biomarkers which related with the bone turnover in sickle cell anemia patients. Patients with SCA (n=120) 60 males and 60 females were on follow up in the Basra center for Hereditary Blood Disease, who were included in this study and age and sex matched healthy persons (n=60) as controls. biomarkers had impo...
Background Bone changes are common in sickle cell disease, but the pathogenesis is not fully underst...
Objectives: Sickle bone disease (SBD) is a chronic complication of sickle cell disease (SCD) whose p...
Background: Sickle cell disease (SCD) is the most common inherited monogenic genetic disorder in Ind...
Background: Sickle cell anemia a dangerous genetic disorder in which the erythrocytes of the b...
Objectives (background): Both sickle cell disease and vitamin D deficiency are common among Saudi p...
Background: Sickle cell anemia is a common genetic disease in the world that results from a genetic ...
Background Adult patients with sickle-cell disease (SCD) often have multiple bone compactions causin...
Background: Sickle cell anemia is the most common genetic disease in sub-Saharan Africa. It is an in...
<p><strong>Background:</strong> Cardiac dysfunctions have been recognized as a common complication o...
Objectives: Sickle cell disease has long been associated with bone deformities and pain. Mineral sal...
Objective: This study aims to examine markers of coagulation activation and their possible clinical ...
Objective: The aim of this study was to evaluate the possible roles of fetal hemoglobin levels on bo...
Background: Sickle cell disease (SCD) and its variants are genetic disorders resulting from the pres...
Objectives. Sickle cell anaemia (SCA) is one of the commonest genetic disorders in the world. It is ...
Background: Sickle cell disease was a genetic pathology of the red blood cell, which caused systemic...
Background Bone changes are common in sickle cell disease, but the pathogenesis is not fully underst...
Objectives: Sickle bone disease (SBD) is a chronic complication of sickle cell disease (SCD) whose p...
Background: Sickle cell disease (SCD) is the most common inherited monogenic genetic disorder in Ind...
Background: Sickle cell anemia a dangerous genetic disorder in which the erythrocytes of the b...
Objectives (background): Both sickle cell disease and vitamin D deficiency are common among Saudi p...
Background: Sickle cell anemia is a common genetic disease in the world that results from a genetic ...
Background Adult patients with sickle-cell disease (SCD) often have multiple bone compactions causin...
Background: Sickle cell anemia is the most common genetic disease in sub-Saharan Africa. It is an in...
<p><strong>Background:</strong> Cardiac dysfunctions have been recognized as a common complication o...
Objectives: Sickle cell disease has long been associated with bone deformities and pain. Mineral sal...
Objective: This study aims to examine markers of coagulation activation and their possible clinical ...
Objective: The aim of this study was to evaluate the possible roles of fetal hemoglobin levels on bo...
Background: Sickle cell disease (SCD) and its variants are genetic disorders resulting from the pres...
Objectives. Sickle cell anaemia (SCA) is one of the commonest genetic disorders in the world. It is ...
Background: Sickle cell disease was a genetic pathology of the red blood cell, which caused systemic...
Background Bone changes are common in sickle cell disease, but the pathogenesis is not fully underst...
Objectives: Sickle bone disease (SBD) is a chronic complication of sickle cell disease (SCD) whose p...
Background: Sickle cell disease (SCD) is the most common inherited monogenic genetic disorder in Ind...