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Thalassemia (severe form)
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Publications (1158)
- Probable sarcopenia and bone health in transfusion-dependent beta thalassemia patients. (2026/12/31) ♡
- Th1/Th2 cytokine imbalance with novel IL-17F elevation in Iraqi transfusion-dependent beta-thalassemia: a dual-platform diagnostic study. (2026/09/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Precision Medicine in Transfusion-Dependent and Non-Transfusion-Dependent β-Thalassemia: Toward Personalized Diagnosis and Therapy. (2026/08/10) ♡
- CRISPR-Cas12a Gene Editing of HBG1 and HBG2 Promoters to Treat β-Thalassemia. (2026/08/06) ♡
- Single-Molecule Real-Time Sequencing Reveals Hidden Diversity and Corrects Misdiagnosis in α-Thalassemia. (2026/08/05) ♡
- Determinants of liver stiffness assessed by transient elastography in transfusion-dependent thalassemia. (2026/08/05) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Biomarker implications of gene editing in hematologic diseases: latest updates from ASH 2025. (2026/08/05) ♡
- Mitapivat (Aqvesme) for thalassemia. (2026/08/03) ♡
- Pulmonary hypertension in beta-thalassaemia: methodological considerations and future directions. (2026/08/03) ♡
- Three-Dimensional Craniofacial Characteristics in Transfusion-Dependent and Non-Transfusion-Dependent Thalassemia Patients. (2026/08/01) ♡
- Liver Diffusion Weighted MRI: Effect of Iron Overload on Apparent Diffusion Coefficient. (2026/08/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Evaluating mitapivat for the treatment of alpha or beta thalassemia. (2026/08/01) ♡
- α- and β-Thalassemia Show Distinct Bone Microarchitectural Phenotypes in Southeast Asian Adults: Associations with Marrow Expansion Phenotype. (2026/07/31) ♡
- Genotype-Phenotype Correlation of Β-Globin Mutations and Hematological Parameters in Iraqi Β-Thalassemia Patients. (2026/07/31) ♡
- Association Between IL-10 and Serum Hepcidin in Patients with β-Thalassemia Major: A Case-Control Study Using Multiple Statistical Modeling. (2026/07/30) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Associations of anti-Müllerian hormone with primordial follicle density and in vitro maturation outcomes in girls with transfusion-dependent thalassemia undergoing fertility preservation. (2026/07/28) ♡
- Public knowledge, attitudes, and ethical views on CRISPR-Cas9 gene editing for genetic diseases in Taif, Saudi Arabia. (2026/07/28) ♡
- Life Participation and Adaptive Functioning of Immigrant and Non-Immigrant Children with β-Thalassemia in Turkiye: An ICF-Based Study. (2026/07/28) ♡
- Expression Differences of Abnormal Hemoglobin New York in Infants, Children and Adults, and Analysis of Clinical Phenotypes and Genotypes in Combination with Thalassemia. (2026/07/27) ♡
- Genetic Analysis of Two Patients with Compound Thalassemia Presenting with Elevated HbF and Normal HbA(2) Levels. (2026/07/27) ♡
- Humanistic and economic burden among caregivers of adults and children with transfusion dependent β-thalassemia: a mixed-methods study. (2026/07/26) ♡
- Fludarabine, Busulfan, Thiotepa, and Melphalan: A Novel Low-Toxicity Myeloablative Conditioning Regimen for Haploidentical HSCT in Children and Adolescents Aged ≥7 Years With Transfusion-Dependent β-Thalassemia. (2026/07/23) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Diagnosis and Management of Transfusion-Dependent Thalassemia: Evidence-Based Guidelines From the Pediatric Hematology Oncology Chapter of the Indian Academy of Pediatrics. (2026/07/23) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Transfusion-dependent changes to hemoglobin A(1c) in a beta-thalassemia major patient. (2026/07/22) ♡
- Prenatal diagnosis of hemoglobinopathies by chorionic villus sampling: A large single-center experience. (2026/07/22) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Base editing for precision therapeutics. (2026/07/22) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Postpartum Atypical Hemolytic Uremic Syndrome Complicating β-Thalassemia Intermedia: A Case Report and Literature Review. (2026/07/22) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Crohn's disease and ulcerative colitis in β-thalassemia major: A report of two cases and a brief review of the literature. (2026/07/22) ♡
- Between scarcity and surfeit: a familial tale of contradictory iron disorders (β-thalassemia and iron-refractory iron deficiency anemia). (2026/07/21) ♡
- Structure-guided targeting of the GATAD2A-CHD4 interaction within the MBD2-NuRD complex results in high levels of HbF in adult erythroid cells. (2026/07/20) ♡
- Update of the decision-making algorithm on selecting transfusion-dependent β-thalassemic patients for gene therapy approaches: joint consensus report on behalf of EHA-specialized working group and EBMT hemoglobinopathies working party. (2026/07/16) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Red lines and green lights: Gene therapy for inherited erythroid disorders beyond the haemoglobinopathies. (2026/07/14) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Activin Signaling Inhibitors in Pulmonary Hypertension: A State-of-the-Art Review. (2026/07/14) ♡
- Molecular Epidemiology of Thalassemia in University Town, Chongqing: Spectrum of Pathogenic Variants and Implications for Carrier Screening. (2026/07/14) ♡
- Molecular Epidemiology of δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin (HPFH) in the Quanzhou Childbearing-Age Population, China. (2026/07/13) ♡
- Seroprevalence of human T-cell lymphotropic virus and transfusion-transmitted viral hepatitis markers among hemodialysis and thalassemia patients in the South of Iran. (2026/07/13) ♡
- Development of a New Portable Genetic Analyzer for Point-of-Care Molecular Genetics and Pharmacogenomics Analysis. (2026/07/12) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. [Phenotypic modification of β-Thalassemia by variants of SUPT5H gene: Report of two pedigrees and a literature review]. (2026/07/10) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Thalassaemia. (2026/07/09) ♡
- Non-genotoxic transplantation and in vivo selection through epitope editing. (2026/07/08) ♡
- Familial Aggregation and Poor Childhood Survival in Thalassemia Despite Early Diagnosis: A Longitudinal Study From Balochistan, Pakistan. (2026/07/08) ♡
- CD117 epitope-shielded hematopoietic stem cell transplantation with toxin-free conditioning and in vivo selection ameliorates a β-thalassemia model. (2026/07/08) ♡
- Assessment of Myocardial Iron Overload and Strain Abnormalities in Pediatric β-Thalassemia Using Multiparametric CMR. (2026/07/08) ♡
- Fish-shaped erythrocytes and pincer cells co-occur in distinct hematological disorders and are associated with anemia severity. (2026/07/07) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Luspatercept Induces Significant Improvement in Anemia in Dominant Thalassemia Secondary to Heterozygous STEAP3 and Beta-Thalassemia Trait. (2026/07/07) ♡
- Unlocking thalidomide response as a hemoglobin F augmentation agent in transfusion-dependent β-thalassemia: the genetic impact of BCL11A, HBS1L-MYB, and XmnI polymorphism. (2026/07/07) ♡
- Application of Cell-Free DNA Barcode-Enabled Single-Molecule Test for Non-Invasive Prenatal Testing of α-Thalassemia and β-Thalassemia. (2026/07/05) ♡
- Appropriateness of β-thalassemia trait screening in patients with hypochromic microcytic anemia and predictors of potentially low-yield testing. (2026/07/05) ♡
- Low- to moderate-dose thalidomide combination rescue after luspatercept failure in transfusion-dependent β-thalassemia: a real-world cohort study. (2026/07/03) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Adipsic hypernatremia associated with hypothalamic dysfunction and sleep disorders. (2026/07/02) ♡
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