Most Cited & Viewed

Most Cited & Viewed Papers

Citations Article
 
Hemoglobin Disorders in Europe: A Systematic Effort of Identifying and Addressing Unmet Needs and Challenges by the Thalassemia International Federation
 
Hb Mazandaran (α1) α51 Gly > Cys(CE9), c.154 GGC > TGC: A Novel Haemoglobin Variant of α1-Globin Gene
 
Peripheral Blood Erythrocyte Parameters in Β-Thalassemia Minor with Coexistent Iron Deficiency: Comparisons between Iron-Deficient and -Sufficient Carriers
 
Co-Inheritance of Heterozygous β0-Thalassemia with Single Functional α-Globin Gene: Challenges of Carrier Detection in Pre-Marital Screening Program for Thalassemia
 
Redesigning New Policy Options for Thalassemia Prevention in Sri Lanka
 
Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment
 
The First Case of Haemophagocytic Lymphohistiocytosis Triggered by the Booster Dose of Anti-SARS-CoV-2 Vaccine in a Patient with β-Thalassemia
 
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
 
Iron Chelation Therapy Needed for Serum Ferritin Overloaded Patients of Beta Thalassemia Major
 
A Patient with Sickle Cell Disease and Recurrent Venous Thromboembolism after Renal Transplantation
Views Article
CRISPR Gene Therapy: A Promising One-Time Therapeutic Approach for Transfusion-Dependent β-Thalassemia—CRISPR-Cas9 Gene Editing for β-Thalassemia
Cardiovascular Complications in β-Thalassemia: Getting to the Heart of It
Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment
HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients
Is the Role of Hepcidin and Erythroferrone in the Pathogenesis of Beta Thalassemia the Key to Developing Novel Treatment Strategies?
Relationships among Physical Activity, Pain, and Bone Health in Youth and Adults with Thalassemia: An Observational Study
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
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)
Highlights on the Luspatercept Treatment in Thalassemia
Redesigning New Policy Options for Thalassemia Prevention in Sri Lanka
Downloads Article
Hemoglobin Disorders in Europe: A Systematic Effort of Identifying and Addressing Unmet Needs and Challenges by the Thalassemia International Federation
CRISPR Gene Therapy: A Promising One-Time Therapeutic Approach for Transfusion-Dependent β-Thalassemia—CRISPR-Cas9 Gene Editing for β-Thalassemia
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
Going Back to Fundamentals: Three Marriageable Actions for Thalassemia and Carrier Population Management
Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment
Redesigning New Policy Options for Thalassemia Prevention in Sri Lanka
Is the Role of Hepcidin and Erythroferrone in the Pathogenesis of Beta Thalassemia the Key to Developing Novel Treatment Strategies?
Cardiovascular Complications in β-Thalassemia: Getting to the Heart of It
Molecular Heterogeneity of Hb H Disease in India
Iron Chelation Therapy Needed for Serum Ferritin Overloaded Patients of Beta Thalassemia Major
Back to TopTop