Thalassemia (severe form)
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Publications (1159)
- Patra index and Mentzer index - A retrospective comparative study to differentiate Beta-Thalassemia Trait from iron deficiency anemia. (2025/11/01) ♡
- The Utility of HbA1c and Fructosamine in Evaluating the Glucose Tolerance in Adult Patients with Transfusion-Dependent Beta-Thalassemia. (2025/11/01) ♡
- Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. Genetic patterns & public health implications of sickle cell anaemia across populations: A systematic review. (2025/11/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A Case Report of HLA 5/10 Cord Blood Cell Engraftment in a Patient with Severe β Thalassemia after Haplo-Cord Stem Cell Transplantation. (2025/11/01) ♡
- Impact of transferrin levels on iron accumulation in transfusion-dependent beta-thalassemia: A genotype-specific analysis. (2025/10/28) ♡
- Early thalassemia screening via hemoglobin β-subunit detection: a portable PDA-PoPD-MWCNT electrochemical immunosensor. (2025/10/23) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Chelation: The Double-Edged Sword. A Case Report of Invasive, Disseminated Mucor Mycosis in a Beta Thalassemia Major During Transplant. (2025/10/01) ♡
- Dietary Patterns Among Patients With Beta-Thalassemia Major in Vietnam. (2025/10/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Clinico-epidemiological Profile of Transfusion-dependent Thalassemia Patients in a Tertiary Care Children's Hospital in Nepal: An Observational Study. (2025/10/01) ♡
- 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. Genetic Engineering in Hematopoietic Stem Cells for β-Hemoglobinopathies Treatment: Advances, Challenges, and Clinical Translation. (2025/10/01) ♡
- Expression of the FAM132B Gene in Iranian Patients with Beta-Thalassemia. (2025/10/01) ♡
- Dysregulated Expression of miR-222 and miR-15a in Transfusion-Dependent Thalassemia: Associations with Torque Teno Virus and Cytomegalovirus Infections. (2025/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Novel HBB:c.375_376delAC mutation in a Malay patient with HbE beta-thalassemia intermedia: A case report. (2025/09/26) ♡
- Pulsed electric field (PEF)-processed 6-shogaol-rich ginger extract protects β-Thalassemic red blood cells from iron-induced oxidative stress and hemolysis. (2025/09/12) ♡
- 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. Genosomes: An Introspection into Transfection, Future Perspectives and Applications. (2025/09/09) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Blood that was far from red: hypertriglyceridaema thalassaemia syndrome: case report. (2025/09/01) ♡
- Gut microbiota-derived TMAO and SIRT1/HMGB1 Axis: unveiling mechanisms of renal impairment in beta-thalassemia major. (2025/08/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sickle cell β-thalassemia diagnosed at age 40: a case report. (2025/08/01) ♡
- Circulating Red Cell and Platelet Microparticles in Pediatric Non-transfusion Dependent Beta-thalassemia: A Case Control Study. (2025/07/31) ♡
- Risk factors of low bone mass in young patients with transfusion-dependent beta-thalassemia. (2025/07/02) ♡
- 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. Gene therapy for sickle cell disease: recent advances, clinical trials and future directions. (2025/07/01) ♡
- Mutation Analysis for Hemoglobinopathies in Eastern Jharkhand. (2025/07/01) ♡
- Characterisation of β-thalassemia mutations in a tertiary care referral hospital in southern India- A descriptive study. (2025/07/01) ♡
- Assessment of Serum Autophagy Related Protein Beclin-1 in Egyptian Adult Beta Thalassemia Patients. (2025/07/01) ♡
- Alpha-Thalassemia Caused by αα(IVSI-1(AGGT> AGAT)) (HBA1: c.95 + 1G > A) Mutation and its Combinations with Other Forms of Thalassemia or Hemoglobinopathy in Northern Thailand. (2025/07/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Unraveling complexity: A case report on ABO hemolytic disease of the fetus newborn in a preterm neonate and delayed hemolytic transfusion reaction in the beta thalassemic mother due to alloanti kidd a antibody. (2025/07/01) ♡
- Randomized researchiParticipants were divided into groups by lottery and compared with each other. This reduces the chance that a difference is due to something other than the treatment. Oxidative stress markers and tissue iron overload after 12-months vitamin E supplementation for children with transfusion-dependent β-thalassemia on different iron chelators: A randomized placebo-controlled trial. (2025/07/01) ♡
- Comprehensive expression of long non-coding RNAs and association with iron and erythropoiesis regulatory proteins in transfusion-dependent β-thalassemia. (2025/06/22) ♡
- Correlation between vitamin D level and left ventricular myocardial function demonstrated by speckle tracking echocardiography among β-thalassemia major children. (2025/06/16) ♡
- Mapping anemia prevalence across Indonesia. (2025/06/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Zinc level and its impact on the phenotype of sickle cell disease. (2025/06/01) ♡
- Randomized researchiParticipants were divided into groups by lottery and compared with each other. This reduces the chance that a difference is due to something other than the treatment. Measures of cellular oxidative damage following vitamin E supplementation in young patients with transfusion-dependent thalassemia: a double-blind randomized controlled trial. (2025/05/20) ♡
- Reduced GATA1 levels are associated with ineffective erythropoiesis in sickle cell anemia. (2025/05/01) ♡
- A Variable Clinical Presentation of Hemoglobin City of Hope. (2025/05/01) ♡
- Evaluating Renal Glomerular Function in Beta-Thalassemia Patients Receiving Deferasirox Using Serum Cystatin-C and Creatinine: A Cross-Sectional Study. (2025/05/01) ♡
- Hb Monza: A novel extensive HBB duplication with preserved α-β subunit interaction and unstable hemoglobin phenotype. (2025/04/11) ♡
- Serum folate and dietary folate intake in beta thalassaemia trait: a case-control study from Sri Lanka. (2025/04/08) ♡
- 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. Therapeutic potential of synthetic and natural iron chelators against ferroptosis. (2025/04/01) ♡
- Molecular Characterization of δβ Thalassemia/Hereditary Persistence of Fetal Hemoglobin and Its Correlation With Clinical and Hematological Profile; a Single Center Study in North India. (2025/04/01) ♡
- An In-Depth Analysis of Variable Dynamics Influencing Bone Mineral Density in Transfusion-Dependent Thalassemia Patients. (2025/04/01) ♡
- A Comprehensive Gap Analysis of Risk Factors for Transfusion Dependent Thalassemia in Siblings. (2025/04/01) ♡
- The effect of aqueous extract of Iranian oak (Quercus brantii) on lipid profile and liver enzymes in beta-thalassemia patients: a randomized controlled trial, double-blind, placebo-controlled. (2025/03/26) ♡
- Hypoparathyroidism in adults with iron overload diseases (IOD): evidence of a subclinical phenotype. (2025/03/01) ♡
- Iron-responsive nanoparticle-loaded bilayer dissolving microneedles for selective and controlled transdermal delivery of deferasirox in β-thalassemia major treatment. (2025/03/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Evaluating the Role of Red Blood Cell Lifespan in Transfusion-Dependent β-Thalassemia and Impact of Thalidomide Treatment. (2025/03/01) ♡
- Convolutional neural networks for automatic MR classification of myocardial iron overload in thalassemia major patients. (2025/03/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Early Engraftment and Immune Kinetics Following Allogeneic Transplant Using a Novel Reduced-Toxicity Transplant Strategy in Children/Adolescents with High-Risk Transfusion-Dependent Thalassemia: Early Results of the ThalFAbS Trial. (2025/03/01) ♡
- Haplotype-Resolved Genotyping and Association Analysis of 1,020 β-Thalassemia Patients by Targeted Long-Read Sequencing. (2025/03/01) ♡
- BIA-derived muscle indicator thresholds for malnutrition risk prediction in children with β-thalassemia: a cross-sectional study. (2025/02/27) ♡
- 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. Sickle Cell Disease. (2025/02/13) ♡
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