Executive summary All over the world, people with sickle cell disease (an inherited
condition) have premature deaths and preventable severe chronic complications, which …

Abstract Background Prader–Willi syndrome (PWS) is a complex neuroendocrine disorder
affecting approximately 1/15,000–1/30,000 people. Unmet medical needs of individuals with …

The transfusion of red blood cells (RBCs) is a crucial treatment for sickle cell disease (SCD).
While often beneficial, the frequent use of transfusions is associated with numerous …

Sickle cell disease (SCD) is a group of inherited autosomal recessive disorders, including
sickle cell anemia, sickle beta-thalassemia, and other hemoglobinopathies, which are …

Adverse pregnancy outcomes occur frequently in women with sickle cell disease (SCD)
across the globe. In the United States, Black women experience disproportionately worse …

Pregnancy in women with sickle cell disease (SCD) is associated with increased maternal
and fetal morbidity and mortality. Outcomes vary widely owing to methodological limitations …

Background: Pulmonary complications of sickle cell disease (SCD) are diverse and
encompass acute and chronic disease. The understanding of the natural history of …

Sickle Cell Disease (SCD) is among the most common single-gene diseases in the world
but evidence-based comprehensive health care has not been implemented where the …

Objective The aim of the study is to identify quantitative evidence for the efficacy of
interprofessional learning (IPL) to improve patient outcomes. Methods We conducted a …

Background Reducing preterm birth and stillbirth and improving outcomes for babies born
too soon is essential to reduce under-5 mortality globally. In the context of a rapidly evolving …