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
Modifying quality and equity of care: emerging roles of genetic disease modifiers in β-hemoglobinopathies. [PDF]
Papasavva PL +9 more
europepmc +1 more source
HELIOS Action: Advancing research, education, and equity in hemoglobinopathies across Europe and beyond. [PDF]
Chatzimatthaiou S +22 more
europepmc +1 more source
Silent sicklers and traumatic hyphema: the importance of maintaining a high index of suspicion. [PDF]
Pratt J +5 more
europepmc +1 more source
End-of-Life Care in Sickle Cell Disease and Transfusion-Dependent β-Thalassemia: Clinical, Psychosocial, and Ethical Considerations. [PDF]
Delicou S +3 more
europepmc +1 more source
Adaptive Immune Remodeling in Sickle Cell Disease: Linking Hemolysis-Driven Inflammation to Immune Dysfunction. [PDF]
Jamwal S +6 more
europepmc +1 more source
A retrospective cross-sectional study on newborn screening and prevalence of disorders among UAE population. [PDF]
Shafique K +9 more
europepmc +1 more source

