The high childhood mortality and life-long complications associated with sickle cell anemia (SCA) in developing countries could be significantly reduced with effective prophylaxis and education if SCA is diagnosed early in life. However, conventional laboratory methods used for diagnosing SCA remain prohibitively expensive and impractical in this setting. This study describes the clinical validation of a low-cost paper-based test for SCA that can accurately identify sickle trait carriers (HbAS) and individuals with SCA (HbSS) among adults and children over 1 year of age
Objective. To determine the cost benefit of screening for sickle-cell disease among infants at distr...
Systematic review of newborn screening programs for sickle cell anemia in sub-Saharan Africa. Sarah...
Objective: Sickle cell disease (SCD) is a common hereditary disease in Iran. In developed countries...
The high childhood mortality and life-long complications associated with sickle cell anemia (SCA) in...
Background The high childhood mortality and life-long complications associated with sickle cell anem...
Background: Sickle cell disease is one of the most common inherited blood disorders. Universal scree...
A rapid test to identify patients with sickle cell disease could have important benefits in low-reso...
Introduction: Sickle-cell disease (SCD) refers to a group of inherited disorders affecting hemoglobi...
Sickle cell anemia (SCA) is a genetic blood disorder that is particularly lethal in early childhood....
BACKGROUND: Sickle cell disease (SCD) describes a group of inherited red blood cell disorders. Peopl...
A rapid test to identify patients with sickle cell disease could have important benefits in low-reso...
An accurate and affordable test for the rapid diagnosis of sickle cell disease could revolutionize t...
Sickle cell disease is a hereditary disease that predominantly affects black people. It is very wide...
Quantification of sickle hemoglobin (HbS) in patients with sickle cell disease (SCD) undergoing hydr...
Background: Sickle cell trait (SCT) screening is required at birth in the United States; however, ad...
Objective. To determine the cost benefit of screening for sickle-cell disease among infants at distr...
Systematic review of newborn screening programs for sickle cell anemia in sub-Saharan Africa. Sarah...
Objective: Sickle cell disease (SCD) is a common hereditary disease in Iran. In developed countries...
The high childhood mortality and life-long complications associated with sickle cell anemia (SCA) in...
Background The high childhood mortality and life-long complications associated with sickle cell anem...
Background: Sickle cell disease is one of the most common inherited blood disorders. Universal scree...
A rapid test to identify patients with sickle cell disease could have important benefits in low-reso...
Introduction: Sickle-cell disease (SCD) refers to a group of inherited disorders affecting hemoglobi...
Sickle cell anemia (SCA) is a genetic blood disorder that is particularly lethal in early childhood....
BACKGROUND: Sickle cell disease (SCD) describes a group of inherited red blood cell disorders. Peopl...
A rapid test to identify patients with sickle cell disease could have important benefits in low-reso...
An accurate and affordable test for the rapid diagnosis of sickle cell disease could revolutionize t...
Sickle cell disease is a hereditary disease that predominantly affects black people. It is very wide...
Quantification of sickle hemoglobin (HbS) in patients with sickle cell disease (SCD) undergoing hydr...
Background: Sickle cell trait (SCT) screening is required at birth in the United States; however, ad...
Objective. To determine the cost benefit of screening for sickle-cell disease among infants at distr...
Systematic review of newborn screening programs for sickle cell anemia in sub-Saharan Africa. Sarah...
Objective: Sickle cell disease (SCD) is a common hereditary disease in Iran. In developed countries...