CCND3 Suppression Ameliorates β-Thalassaemia in a Murine Disease Model: A Potential Therapeutic Strategy. [PDF]
Caria CA +9 more
europepmc +1 more source
Real-world complication burden and disease management paradigms in transfusion-related β-thalassaemia in Greece: Results from ULYSSES, an epidemiological, multicentre, retrospective cross-sectional study. [PDF]
Kattamis A +14 more
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Red blood cell membrane proteome as a reporter of disease severity, transfusion impact and genetic background in transfusion-dependent β-thalassaemia. [PDF]
Theocharaki K +8 more
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Deferiprone therapy improves the oxidative status of LDL in patients with β-thalassaemia/HbE. [PDF]
Tran NT +6 more
europepmc +1 more source
Ineffective Erythropoiesis in β-Thalassaemia: Key Steps and Therapeutic Options by Drugs. [PDF]
Longo F, Piolatto A, Ferrero GB, Piga A.
europepmc +1 more source
Evaluation of β-Thalassaemia Cases for Common Mutations in Western Rajasthan. [PDF]
Purohit A +5 more
europepmc +1 more source
Cytochemical observations on β-thalassaemia
The question of the Periodic-Acid Schiff positive material in the normoblasts of homozygous β-thalassacmia and related conditions has been reexamined. The staining properties and mainly the degradation by diastase indicate that this PAS positive material
Papayannopoulou, T., Fessas, P.
core
Evaluation of Five Plasma miRNAs as Biomarkers for Minimally Invasive Staging of Liver Fibrosis in β-Thalassaemia Patients. [PDF]
Özkaramehmet S +14 more
europepmc +1 more source
Clinical patterns of thalidomide in the treatment of transfusion-dependent β-thalassaemia in children: a prospective single-arm study in China. [PDF]
Li X +10 more
europepmc +1 more source
Extracellular vesicles modulate endothelial nitric oxide production in patients with β‑thalassaemia/HbE. [PDF]
Phongpao K +9 more
europepmc +1 more source

