Targeted protein degradation for fetal hemoglobin induction: a new paradigm in β-hemoglobinopathy therapy. [PDF]
Biomark ResArji S +12 more
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End-of-Life Care in Sickle Cell Disease and Transfusion-Dependent β-Thalassemia: Clinical, Psychosocial, and Ethical Considerations. [PDF]
Mediterr J Hematol Infect DisDelicou S +3 more
europepmc +1 more source
Hemoglobinopathies are a group of severe hereditary blood diseases caused by a violation of the structure of hemoglobin or a decrease in the synthesis of one or more globin chains. The clinical picture is extremely varied. Common symptoms are hemolytic anemia, enlarged spleen, and bone damage.
openaire +2 more sources
Beyond Iron Deficiency: An Atypical Peripheral Smear Revealing Hemoglobin C in an Adolescent. [PDF]
CureusHamidine M, Awati M, Mehdi A.
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Decoding thalassemia and sickle cell disease: advances in molecular technologies for comprehensive variant detection. [PDF]
Front GenetFoord E +7 more
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Pregnancy-Triggered Vaso-Occlusive Crises in Hemoglobin SE Disease Complicated by Glucose-6-Phosphate Dehydrogenase Deficiency: A Case Report. [PDF]
CureusAlzahrani LM, Altassan FF, Althubaity W.
europepmc +1 more source
Bilateral Peripheral Neovascularization in Hemoglobin C Trait Retinopathy. [PDF]
J Vitreoretin DisJabara J +3 more
europepmc +1 more source
Atypical Overt Hemorrhagic Stroke in an Adult With Sickle Cell-Hemoglobin C Disease: A Report of a Rare Case. [PDF]
CureusManjrekar NS +3 more
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Factors associated with anemia among adolescent girls in Western India: insights from a multi-centric cross-sectional study. [PDF]
Front Glob Womens HealthJoshi K +10 more
europepmc +1 more source