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Еквивалентен фонетика Асер cappellini and thalassemia treatments haematologica 2017 Нарушават Северозападна пола

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

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

Safety and efficacy of thalidomide in patients with transfusion-dependent β- thalassemia: a randomized clinical trial | Signal Transduction and Targeted  Therapy
Safety and efficacy of thalidomide in patients with transfusion-dependent β- thalassemia: a randomized clinical trial | Signal Transduction and Targeted Therapy

Frontiers | New Insights Into Pathophysiology of β-Thalassemia
Frontiers | New Insights Into Pathophysiology of β-Thalassemia

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

An urgent need for improving thalassemia care due to the wide gap in  current real-life practice and clinical practice guidelines | Scientific  Reports
An urgent need for improving thalassemia care due to the wide gap in current real-life practice and clinical practice guidelines | Scientific Reports

Current and future alternative therapies for beta-thalassemia major -  ScienceDirect
Current and future alternative therapies for beta-thalassemia major - ScienceDirect

New treatment strategies for β-thalassemia | Encyclopedia MDPI
New treatment strategies for β-thalassemia | Encyclopedia MDPI

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

A paradigm shift on beta-thalassaemia treatment: How will we manage this  old disease with new therapies? - ScienceDirect
A paradigm shift on beta-thalassaemia treatment: How will we manage this old disease with new therapies? - ScienceDirect

Full article: Revisiting beta thalassemia intermedia: past, present, and  future prospects
Full article: Revisiting beta thalassemia intermedia: past, present, and future prospects

Beta Thalassemia: Practice Essentials, Etiology, Epidemiology
Beta Thalassemia: Practice Essentials, Etiology, Epidemiology

Antioxidants as Complementary Medication in Thalassemia | IntechOpen
Antioxidants as Complementary Medication in Thalassemia | IntechOpen

Quality of life in patients with β‐thalassemia: A prospective study of  transfusion‐dependent and non‐transfusion‐dependent patients in Greece,  Italy, Lebanon, and Thailand - Cappellini - 2019 - American Journal of  Hematology - Wiley
Quality of life in patients with β‐thalassemia: A prospective study of transfusion‐dependent and non‐transfusion‐dependent patients in Greece, Italy, Lebanon, and Thailand - Cappellini - 2019 - American Journal of Hematology - Wiley

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

Sirolimus for Treatment of β-Thalassemia: From Pre-Clinical Studies to the  Design of Clinical Trials
Sirolimus for Treatment of β-Thalassemia: From Pre-Clinical Studies to the Design of Clinical Trials

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

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

Tricuspid-valve regurgitant jet velocity as a risk factor for death in β- thalassemia | Haematologica
Tricuspid-valve regurgitant jet velocity as a risk factor for death in β- thalassemia | Haematologica

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

Pathophysiology and treatment of patients with... | F1000Research
Pathophysiology and treatment of patients with... | F1000Research

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

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