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Coordinated β-globin expression and α2-globin reduction in a multiplex  lentiviral gene therapy vector for β-thalassemia: Molecular Therapy
Coordinated β-globin expression and α2-globin reduction in a multiplex lentiviral gene therapy vector for β-thalassemia: Molecular Therapy

Frontiers | The Future of Gene Therapy for Transfusion-Dependent Beta- Thalassemia: The Power of the Lentiviral Vector for Genetically Modified  Hematopoietic Stem Cells
Frontiers | The Future of Gene Therapy for Transfusion-Dependent Beta- Thalassemia: The Power of the Lentiviral Vector for Genetically Modified Hematopoietic Stem Cells

PDF) Selecting β-thalassemia Patients for Gene Therapy: A Decision-making  Algorithm
PDF) Selecting β-thalassemia Patients for Gene Therapy: A Decision-making Algorithm

Replacing the suppressed hormone: toward a better treatment for iron  overload in β-thalassemia major? | Haematologica
Replacing the suppressed hormone: toward a better treatment for iron overload in β-thalassemia major? | Haematologica

Gene therapies for transfusion dependent β‐thalassemia: Current status and  critical criteria for success - Soni - 2020 - American Journal of  Hematology - Wiley Online Library
Gene therapies for transfusion dependent β‐thalassemia: Current status and critical criteria for success - Soni - 2020 - American Journal of Hematology - Wiley Online Library

Pediatric Thalassemia: Practice Essentials, Background, Pathophysiology
Pediatric Thalassemia: Practice Essentials, Background, Pathophysiology

Guidelines for the Management of Transfusion-Dependent Thalassaemia (4th  Edition - Version 2.0) by Thalassaemia International Federation (TIF) -  Issuu
Guidelines for the Management of Transfusion-Dependent Thalassaemia (4th Edition - Version 2.0) by Thalassaemia International Federation (TIF) - Issuu

Cure for thalassemia major – from allogeneic hematopoietic stem cell  transplantation to gene therapy | Haematologica
Cure for thalassemia major – from allogeneic hematopoietic stem cell transplantation to gene therapy | Haematologica

β-Thalassemia | Genetics in Medicine
β-Thalassemia | Genetics in Medicine

JCM | Free Full-Text | Does Hepcidin Tuning Have a Role among Emerging  Treatments for Thalassemia?
JCM | Free Full-Text | Does Hepcidin Tuning Have a Role among Emerging Treatments for Thalassemia?

Novel genetic therapeutic approaches for modulating the severity of β‑ thalassemia (Review)
Novel genetic therapeutic approaches for modulating the severity of β‑ thalassemia (Review)

PDF] Current and future alternative therapies for beta-thalassemia major |  Semantic Scholar
PDF] Current and future alternative therapies for beta-thalassemia major | Semantic Scholar

PDF) Cure for thalassemia major – From allogeneic hematopoietic stem cell  transplantation to gene therapy
PDF) Cure for thalassemia major – From allogeneic hematopoietic stem cell transplantation to gene therapy

Guidelines for the Management of Non-Transfusion Dependent Thalassaemias  (2nd edition - 2017) by Thalassaemia International Federation (TIF) - Issuu
Guidelines for the Management of Non-Transfusion Dependent Thalassaemias (2nd edition - 2017) by Thalassaemia International Federation (TIF) - Issuu

Frontiers | The Future of Gene Therapy for Transfusion-Dependent Beta- Thalassemia: The Power of the Lentiviral Vector for Genetically Modified  Hematopoietic Stem Cells
Frontiers | The Future of Gene Therapy for Transfusion-Dependent Beta- Thalassemia: The Power of the Lentiviral Vector for Genetically Modified Hematopoietic Stem Cells

Cureus | Improving Ineffective Erythropoiesis in Thalassemia: A Hope on the  Horizon | Article
Cureus | Improving Ineffective Erythropoiesis in Thalassemia: A Hope on the Horizon | Article

Diseases | Free Full-Text | Luspatercept: A New Tool for the Treatment of  Anemia Related to β-Thalassemia, Myelodysplastic Syndromes and Primary  Myelofibrosis
Diseases | Free Full-Text | Luspatercept: A New Tool for the Treatment of Anemia Related to β-Thalassemia, Myelodysplastic Syndromes and Primary Myelofibrosis

Frontiers | Genetic and Epigenetic Therapies for β-Thalassaemia by Altering  the Expression of α-Globin Gene
Frontiers | Genetic and Epigenetic Therapies for β-Thalassaemia by Altering the Expression of α-Globin Gene

Beta Thalassemia: New Therapeutic Options Beyond Transfusion and Iron  Chelation | SpringerLink
Beta Thalassemia: New Therapeutic Options Beyond Transfusion and Iron Chelation | SpringerLink

Biomolecules | Free Full-Text | Epigenetic Insights and Potential Modifiers  as Therapeutic Targets in β–Thalassemia
Biomolecules | Free Full-Text | Epigenetic Insights and Potential Modifiers as Therapeutic Targets in β–Thalassemia

Β-Thalassemias | NEJM
Β-Thalassemias | NEJM

IJMS | Free Full-Text | Thalassemia Intermedia: Chelator or Not?
IJMS | Free Full-Text | Thalassemia Intermedia: Chelator or Not?

Current status of beta‐thalassemia and its treatment strategies - Ali -  2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Current status of beta‐thalassemia and its treatment strategies - Ali - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Β-Thalassemias | NEJM
Β-Thalassemias | NEJM

Survival and complications in patients with haemoglobin E thalassaemia in  Sri Lanka: a prospective, longitudinal cohort study - The Lancet Global  Health
Survival and complications in patients with haemoglobin E thalassaemia in Sri Lanka: a prospective, longitudinal cohort study - The Lancet Global Health