Sociodemographic Determinants of Adherence and Treatment Efficacy in Paediatric Thalassemia Patients from Sarbaz-Rask, Iran

2024-8-15

β-Thalassemia in Bangladesh: Current Status and Future Perspectives

2024-7-8

Premarital Counseling on the Alpha Thalassemia Allele HBA2:c.*94A>G

2024-6-3

Psychological Burden among Pediatric Thalassemia Major Patients in Indonesia: A Review

2024-5-14

Unveiling Extramedullary Hematopoiesis: A Case Report Highlighting the Causes, Symptoms, and Management Strategies

2024-4-10

A Case Report of Hyperhemolytic Syndrome in Sickle Cell Disease, with a Special Focus on Avoiding the Use of Transfusions

2024-3-4

Causes of Hospitalizations in Pediatric Patients with Thalassemia under the National Health Coverage Scheme in Thailand

2024-3-1

Challenges of Iron Chelation in Thalassemic Children

2024-2-1

β Thalassemia Mutation Flow in Indonesia: A Migration Perspective

2023-12-15

Amlodipine Therapy in β-Thalassemia Patients: A Systematic Review and Meta-Analysis on Ferritin Levels and Liver MRI T2*

2023-12-11

Association of Bone Disorder and Gene Polymorphism of PPAR-γ Pro12 Ala in Egyptian Children with β-Thalassemia

2023-9-30

Infection and Potential Challenge of Childhood Mortality in Sickle Cell Disease: A Comprehensive Review of the Literature from a Global Perspective

2023-8-30

Association between Glomerular Filtration Rate and β-Thalassemia Major: A Systematic Review and Meta-Analysis

2023-8-29

Understanding the Intricacies of Iron Overload Associated with β-Thalassemia: A Comprehensive Review

2023-7-3

Molecular Epidemiology of HCV Infection among Multi-Transfused β-Thalassemia Patients in Eastern India: A Six-Year Observation

2023-6-25

The Benign Clone Causing Aplastic Anaemia

2023-6-12

HbAdrian (α1:c.251del, p.Leu84Argfs*19)—A Novel Pathogenic Variant in the α1-Globin Gene Associated with Microcytosis from the North of Iran

2023-6-1

What Is the Relevance of Murburn Concept in Thalassemia and Respiratory Diseases?

2023-5-12

Spectrum of Thalassemia and Hemoglobinopathy Using Capillary Zone Electrophoresis: A Facility-Based Single Centred Study at icddr,b in Bangladesh

2023-5-10

Bone Marrow Transplantation in Nonmalignant Haematological Diseases: What Have We Learned about Thalassemia?

2023-4-24

Effect of HFE Gene Mutations on Iron Metabolism of Beta-Thalassemia Carriers

2023-3-17

Impact of Genetic Polymorphisms in Modifier Genes in Determining Fetal Hemoglobin Levels in Beta-Thalassemia

2023-3-16

Highlights on the Luspatercept Treatment in Thalassemia

2023-2-20

New-Generation Ektacytometry Study of Red Blood Cells in Different Hemoglobinopathies and Thalassemia

2023-2-16

CRISPR Gene Therapy: A Promising One-Time Therapeutic Approach for Transfusion-Dependent β-Thalassemia—CRISPR-Cas9 Gene Editing for β-Thalassemia

2023-2-6

Cardiovascular Complications in β-Thalassemia: Getting to the Heart of It

2023-1-30

Juggling between the Cost and Value of New Therapies: Does Science Still Serve Patient Needs?

2023-1-28

Beta-Thalassemia Minor and SARS-CoV-2: Physiopathology, Prevalence, Severity, Morbidity, and Mortality

2023-1-16

TIF Standards for Haemoglobinopathy Reference Centres

2022-12-23

Impact of COVID-19 Pandemic on Pre-Transfusion Hemoglobin Level and Frequency of Transfusion in Transfusion-Dependent Thalassemia Patients in Indonesia

2022-12-22

Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment

2022-11-22

The Outcomes of Patients with Haemoglobin Disorders in Cyprus: A Joined Report of the Thalassaemia International Federation and the Nicosia and Paphos Thalassaemia Centres (State Health Services Organisation)

2022-11-4

Redesigning New Policy Options for Thalassemia Prevention in Sri Lanka

2022-10-19

Is the Role of Hepcidin and Erythroferrone in the Pathogenesis of Beta Thalassemia the Key to Developing Novel Treatment Strategies?

2022-9-9

Going Back to Fundamentals: Three Marriageable Actions for Thalassemia and Carrier Population Management

2022-9-6

Co-Inheritance of Heterozygous β0-Thalassemia with Single Functional α-Globin Gene: Challenges of Carrier Detection in Pre-Marital Screening Program for Thalassemia

2022-8-29

Relationships among Physical Activity, Pain, and Bone Health in Youth and Adults with Thalassemia: An Observational Study

2022-8-11

A Patient with Sickle Cell Disease and Recurrent Venous Thromboembolism after Renal Transplantation

2022-7-20

Molecular Heterogeneity of Hb H Disease in India

2022-7-6

Direct Chromosomal Phasing: An Easy and Fast Approach for Broadening Prenatal Diagnostic Applicability

2022-7-1

Hb Mazandaran (α1) α51 Gly > Cys(CE9), c.154 GGC > TGC: A Novel Haemoglobin Variant of α1-Globin Gene

2022-6-22

The First Case of Haemophagocytic Lymphohistiocytosis Triggered by the Booster Dose of Anti-SARS-CoV-2 Vaccine in a Patient with β-Thalassemia

2022-6-16

Peripheral Blood Erythrocyte Parameters in Β-Thalassemia Minor with Coexistent Iron Deficiency: Comparisons between Iron-Deficient and -Sufficient Carriers

2022-6-6

The Effect of COVID-19 on Hemoglobinopathy Patients’ Daily Lives While Quarantined: Four Greek Hospitals’ Experiences

2022-6-6

Post-COVID-19 Lymphocytopenia and Opportunistic Pathogens Infection in a Thalassemia Major Patient

2022-4-29

Publisher’s Note: Page Numbers Changed to Article Numbers for Articles Published in Thalassemia Reports Volumes 1–11

2022-2-23

Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity

2022-2-18

The New Voice for the New Era of Thalassemia Reports

2022-1-13

HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients

2021-12-15

Publisher’s Note: Continued Publication of Thalassemia Reports by MDPI

2021-12-10