Beta Thalassemia Latest Advances

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: October 28, 2025

Expression of Immune Checkpoints LAG-3, CTLA-4, TIM-3 and PD-1 in Beta Thalassemia patients Treated using HbF Augmentation Therapy and Regular Transfusions.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: October 15, 2025

A Rare Case of Hyperhemolytic Syndrome During Pregnancy.

Journal: Clinical laboratory

Published: October 13, 2025

Filters

Thalassemia and hypercoagulability.

Thalassemia and hypercoagulability.

Base editing of β0-thalassemia mutations as a therapeutic strategy for severe β-hemoglobinopathies.

Base editing of β0-thalassemia mutations as a therapeutic strategy for severe β-hemoglobinopathies.

The Impact of Iron Overload on the Immune System in Patients with β-Thalassemia and Treatment Recommendations --Review

The Impact of Iron Overload on the Immune System in Patients with β-Thalassemia and Treatment Recommendations --Review

Analysis of Thalassemia Gene Variants in the Wuhan Region

Analysis of Thalassemia Gene Variants in the Wuhan Region

Genetic Analysis of a Patient with β-Thalassemia Major and Homozygous Hb Constant Spring in a Chinese Family.

Genetic Analysis of a Patient with β-Thalassemia Major and Homozygous Hb Constant Spring in a Chinese Family.

Frequency of Zinc Deficiency Among Thalassemia Major Patients: A Comparative Cross-Sectional Study.

Frequency of Zinc Deficiency Among Thalassemia Major Patients: A Comparative Cross-Sectional Study.

Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India.

Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India.

Influence of Alpha Thalassaemia on Hematological and Clinical Presentations in Patients of Sickle Cell-β-Thalassaemia with IVS I-5 (G→C) Mutation (HBB: C.20A > T/HBB: C.92 + 5G > C).

Influence of Alpha Thalassaemia on Hematological and Clinical Presentations in Patients of Sickle Cell-β-Thalassaemia with IVS I-5 (G→C) Mutation (HBB: C.20A > T/HBB: C.92 + 5G > C).

Pituitary Versus Hepatic Iron Assessment in Transfusion-Dependent Thalassemia: Is Signal Intensity Ratio a Reliable Tool?

Pituitary Versus Hepatic Iron Assessment in Transfusion-Dependent Thalassemia: Is Signal Intensity Ratio a Reliable Tool?

Low rate of red cell alloimmunization among multiply transfused beta-thalassemia major patients in the Wasit province of Iraq.

Low rate of red cell alloimmunization among multiply transfused beta-thalassemia major patients in the Wasit province of Iraq.

Expression of Immune Checkpoints LAG-3, CTLA-4, TIM-3 and PD-1 in Beta Thalassemia patients Treated using HbF Augmentation Therapy and Regular Transfusions.

Expression of Immune Checkpoints LAG-3, CTLA-4, TIM-3 and PD-1 in Beta Thalassemia patients Treated using HbF Augmentation Therapy and Regular Transfusions.

A Rare Case of Hyperhemolytic Syndrome During Pregnancy.

A Rare Case of Hyperhemolytic Syndrome During Pregnancy.