The integration of the several clinical and laboratory dimensions and the influence of each parameter on the sickle cell disease (SCD)-related mortality is useful for predicting the phenotype of an individual. This study evaluated the feasibility of the SCD severity calculator use to measure disease severity in Brazilian patients. The study group was composed of 500 SCD patients (440 HbSS and 60 HbSC) diagnosed by molecular biology. We observed a decrease in severity scores in 72 SCD patients assessed before and after the hydroxyurea (HU) use. Furthermore, the HU influenced the increase of mean corpuscular volume (MCV) and HbF concentration, and the decrease of leukocytes and total bilirubin. We found 180 (36.0%) patients with intermediate ...
Sickle cell disease is a Public Health problem in Brazil where hemoglobin S has been found in a freq...
OBJECTIVE: Sickle cell anemia and the interaction S/Beta thalassemia differ in hematological values ...
Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present hig...
Modeling the complexity of sickle cell disease pathophysiology and severity is difficult. Using data...
Sickle cell disease (SCD) is a monogenic disorder under polygenic and environmental control. This ae...
There is no instrument to measure severity of sickle cell disease (SCD) in pediatric patients that i...
Objectives: The term sickle cell disease (SCD) is used to describe a group of genetic disorders in w...
AbstractObjectiveThis study aimed to describe and analyze clinical and laboratory characteristics of...
Sickle cell disease (SCD) is characterized by a very heterogeneous clinical ranging from patients wh...
Abstract Objective: This study aimed to describe and analyze clinical and laboratory characteristic...
Background: Sickle cell anemia (SCA) presents a complex pathophysiology which can be affected by a n...
Purpose: Sickle Cell Anaemia (SCA) is an inherited autosomal and lethal blood disorder caused by a m...
BACKGROUND: The development of therapies for sickle cell disease has received special attention, par...
Background: There are documented established markers (indices) of disease severity in patients with ...
BackgroundSickle cell anemia (SCA) is a monogenic hemoglobinopathy associated with severe acute and ...
Sickle cell disease is a Public Health problem in Brazil where hemoglobin S has been found in a freq...
OBJECTIVE: Sickle cell anemia and the interaction S/Beta thalassemia differ in hematological values ...
Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present hig...
Modeling the complexity of sickle cell disease pathophysiology and severity is difficult. Using data...
Sickle cell disease (SCD) is a monogenic disorder under polygenic and environmental control. This ae...
There is no instrument to measure severity of sickle cell disease (SCD) in pediatric patients that i...
Objectives: The term sickle cell disease (SCD) is used to describe a group of genetic disorders in w...
AbstractObjectiveThis study aimed to describe and analyze clinical and laboratory characteristics of...
Sickle cell disease (SCD) is characterized by a very heterogeneous clinical ranging from patients wh...
Abstract Objective: This study aimed to describe and analyze clinical and laboratory characteristic...
Background: Sickle cell anemia (SCA) presents a complex pathophysiology which can be affected by a n...
Purpose: Sickle Cell Anaemia (SCA) is an inherited autosomal and lethal blood disorder caused by a m...
BACKGROUND: The development of therapies for sickle cell disease has received special attention, par...
Background: There are documented established markers (indices) of disease severity in patients with ...
BackgroundSickle cell anemia (SCA) is a monogenic hemoglobinopathy associated with severe acute and ...
Sickle cell disease is a Public Health problem in Brazil where hemoglobin S has been found in a freq...
OBJECTIVE: Sickle cell anemia and the interaction S/Beta thalassemia differ in hematological values ...
Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present hig...