Fujian Province β-Thalassemia: A Molecular and Hematological Study in Southeastern China. [PDF]
Zheng J +8 more
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Hyperhomocysteinemia in pediatric β-thalassemia: links to vitamin cofactor deficiencies and oxidative stress. [PDF]
Dadashova A +4 more
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G2B: an optimized lentiviral vector with enhanced titer and β-globin expression for improved β-thalassemia gene therapy. [PDF]
Gao ZY +11 more
europepmc +1 more source
Total ginsenosides enhance γ-globin expression and fetal hemoglobin production in β-thalassemia models. [PDF]
Cai D +6 more
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Safety and pharmacodynamics of the ferroportin inhibitor vamifeport in patients with non-transfusion-dependent β-thalassemia: results from a randomized phase 2a study. [PDF]
Kattamis A +8 more
europepmc +1 more source
Complete molecular spectrum of β-globin gene mutations via direct sequencing identifies seven novel variants in β-thalassemia major. [PDF]
Sadoon TA, Othman HE.
europepmc +1 more source
Response to Comment on: "A case series of patients with β-thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with miniphlebotomies". [PDF]
Busti F, Girelli D.
europepmc +1 more source
The Masked Thalassemia: A Rare Case of a Patient with Normal HbA2 Levels, β-Thalassemia Pathogenic Variant (CD39 C>T), and a Novel δ-Globin Gene Deletion. [PDF]
Chetta M +10 more
europepmc +1 more source
A standardized extract of Centella asiatica (ECa 233) alleviates brain injury and improves brain function in β-thalassemia mice with iron overload. [PDF]
Yatmark P +6 more
europepmc +1 more source

