Results 111 to 120 of about 35,347 (227)
Compound Heterozygous Sickle Cell-Beta Thalassemia Presenting As Chronic Hemolytic Anemia With Microcytosis and Prominent Left Ventricular Trabeculation: A Case Report. [PDF]
Radhakrishnan VK +4 more
europepmc +1 more source
ABSTRACT Background Pulse oximetry is an accurate diagnostic method for assessing the condition of the dental pulp; however, the normal oxygen saturation levels for each tooth type are yet to be clearly defined. Objectives This systematic review and meta‐analysis aims to answer the question: What are the reference values for pulse oximetry testing in ...
Lilian Tietz +3 more
wiley +1 more source
Iron Overload: Pathophysiology, Diagnosis and Monitoring
ABSTRACT Iron overload is associated with significant health risks, underscoring the importance of understanding its pathophysiology as well as establishing accurate diagnostic and monitoring methods. Chronic iron overload is associated with either genetic disorders characterized by excessive iron accumulation (hereditary hemochromatosis), or is ...
Elena Chatzikalil +3 more
wiley +1 more source
Oral Radiographic Changes in Severe Sickle Cell Anemia Patients: A Retrospective Comparative Study. [PDF]
AlKhodier H +3 more
europepmc +1 more source
This novel qualitative study provides primary data that reflects the sickle cell service user/carer voice about the changes needed to redefine and integrate nutritional management in standard SCD care. ABSTRACT Introduction Nutrition is not currently integrated into standard care provision in sickle cell disease (SCD) impacting patients experience ...
Claudine Matthews +3 more
wiley +1 more source
A rare presentation of hypersplenism in an adult female with homozygous sickle cell disease. [PDF]
Chhetri PK +4 more
europepmc +1 more source
Abstract Background Standardized post‐graduate education in pediatric transfusion medicine remains limited. The objective of this study was to adapt an adult transfusion education program, Transfusion Camp, to include pediatric content and assess knowledge improvement in pediatric subspecialty trainees.
Ines Zuna +14 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
Shooting the messenger: Ecosystem approaches in haematology
HemaSphere, Volume 10, Issue 8, August 2026.
Stephen P. Hibbs
wiley +1 more source
More than malaria: Exploring <i>Babesia</i>, <i>Leishmania</i> and <i>Trypanosoma</i> in sickle cell disease. [PDF]
Bhosale CR +8 more
europepmc +1 more source

