Results 211 to 220 of about 88,496 (299)
Compound Heterozygosity for Hemoglobin S and Hemoglobin LuLu Island
American Journal of Hematology, Volume 101, Issue 7, Page 1440-1442, July 2026.
Dana Lewis +4 more
wiley +1 more source
ABSTRACT Backgrounds and Aims Ultrasound‐based spleen stiffness measurement (SSM) is a valid non‐invasive tool to assess portal hypertension (PH) in chronic liver disease. Whereas the role of the respiratory phase during liver stiffness measurements is established, no study has specifically addressed how respiration influences SSM by transient ...
Sebastiana Atzori +3 more
wiley +1 more source
Heart starts suffering early in sickle cell disease. [PDF]
D'Humières T, De Montalembert M.
europepmc +1 more source
Structural Competency: A Lifeline in a Time of Crisis
ABSTRACT Emergency departments occupy a unique position in the healthcare system: they are often where the consequences of upstream policy manifest most acutely. Structural competency—a framework for understanding how economic, political, and historical forces shape health—offers emergency medicine educators a practical means of preparing trainees to ...
Neelou Weeker +3 more
wiley +1 more source
Buprenorphine for Children and Adolescents with Sickle Cell Disease: A Scoping Review. [PDF]
deBettencourt J +5 more
europepmc +1 more source
High‐Altitude Hypoxemia in Adults With Sickle Cell Disease (SCD)
American Journal of Hematology, Volume 101, Issue 7, Page 1665-1669, July 2026.
Mofiyin A. Obadina +4 more
wiley +1 more source
Asthma screening in children with sickle cell disease in French Guiana. [PDF]
Bafunyembaka G +4 more
europepmc +1 more source
The Longitudinal Effect of APOL1 Risk Alleles on Sickle Cell Anemia‐Associated Kidney Function
ABSTRACT Progressive kidney injury is a major cause of morbidity and mortality in sickle cell anemia (SCA). The high risk APOL1 G1/G2 variants contribute to the development of kidney disease in individuals of African ancestry, including those with SCA.
Sara R. Rashkin +7 more
wiley +1 more source
Sickle cell disease: managing thromboembolism. [PDF]
Babu K, Wun T.
europepmc +1 more source
Unusual Colonic Iron Deposition Following Prophylactic Supplementation in an Infant: A Case Report
ABSTRACT Iron plays a vital role in physiological functions, and its deposition is typically limited to reticuloendothelial tissues in the presence of excess levels. We report a rare case of colonic iron deposition in a 13‐month‐old child without iron overload or toxicity. Despite a normal serum iron profile and administration of only prophylactic iron
Farid Imanzadeh +4 more
wiley +1 more source

