Results 231 to 240 of about 88,496 (299)
Abstract Thalassemia and sickle cell disease (SCD) are among the most common monogenic disorders worldwide. They cause chronic hemolytic anemia, the consequences and prognosis of which vary considerably depending on the genetic characteristics of patients and the healthcare system in their country of residence.
Mariane de Montalembert +19 more
wiley +1 more source
Ferroportin inhibition attenuates pulmonary hypertension in hypoxic sickle cell disease mice. [PDF]
Lucero MJ +23 more
europepmc +1 more source
Abstract Patients with paroxysmal nocturnal hemoglobinuria (PNH) on anti‐C5 often experience extravascular hemolysis with anemia. Iptacopan, the first oral proximal complement inhibitor targeting factor B, has shown efficacy and safety in PNH patients. APPULSE‐PNH (NCT05630001), a phase 3b, single‑arm, open‐label trial, enrolled adult patients with PNH
Austin Kulasekararaj +31 more
wiley +1 more source
Knowledge, Attitude, and Practice of Sickle Cell Disease Among Sickle Cell Disease Patients in Sudurpashchim Province of Nepal: A Cross-Sectional Study. [PDF]
Joshi GD +14 more
europepmc +1 more source
G‐CSF for Mobilizing CD34+ Cells in Individuals With SCD: A Word of Caution
American Journal of Hematology, Volume 101, Issue 6, Page 1178-1181, June 2026.
Akshay Sharma +17 more
wiley +1 more source
Daprodustat augments red cell and γ-globin production in models of sickle cell disease. [PDF]
Sharma M +12 more
europepmc +1 more source
Creative and Adaptive Solutions for Early Diagnosis of Sickle Cell Disease in Sub-Saharan Africa. [PDF]
Smart LR, Segbefia CI, Odame I.
europepmc +1 more source
Clinical, humanistic, and economic burden of sickle cell disease in The Jazan Region, Saudi Arabia. [PDF]
Meraya AM +11 more
europepmc +1 more source
Debunking myths: sickle cell trait, crises, and sudden death
Michael R. DeBaun +2 more
doaj +1 more source

