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Thalassemia (severe form)
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Publications and studies (1521)
- Deep Vein Thrombosis in a Patient With Thalassemia Minor: A Case Report. (2025/11/23) ♡
- Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East Asia. (2025/11/20) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Molecular and structural characterization of a novel β-hemoglobinopathy caused by in Cis β-globin mutations in a Thai individual. (2025/11/20) ♡
- Trabecular bone score in the assessment of bone health in thalassemia major. (2025/11/18) ♡
- MRI-T2(*) quantification of cardiac iron content correlates with extramedullary hematopoiesis and homozygous β0 genotypes in transfusion-dependent thalassemia. (2025/11/18) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Administration of green tea polyphenols mitigates iron-overload-induced bone loss in a β-thalassemia mouse model. (2025/11/18) ♡
- Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia. (2025/11/14) ♡
- 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. Metabolomic Investigation of Myelodysplastic Syndromes, Multiple Myeloma, and Homozygous β-Thalassemia. (2025/11/14) ♡
- Epidemiological Profile of Haemoglobinopathies in Different Districts of West Bengal: A Retrospective Study. (2025/11/11) ♡
- Frequency of Zinc Deficiency Among Thalassemia Major Patients: A Comparative Cross-Sectional Study. (2025/11/10) ♡
- [Genetic screening and typing study of Thalassemia among ethnic Miao Group in Qianxinan area of China]. (2025/11/10) ♡
- Genotypic and hematological profiling of thalassemia in reproductive-age and pediatric populations. (2025/11/07) ♡
- Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India. (2025/11/05) ♡
- Predicting the Double Heterozygotes of HbE and α-Thalassemia-1 (Southeast Asian Type) Using RapidMiner-Generated Hematologic Algorithm. (2025/11/01) ♡
- A Cross-Sectional Study on Pain and Quality of Life of Adult Patients with Transfusion-Dependent Thalassemia in a Tertiary Hospital In Malaysia. (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. Identification of a Patient with Transfusion-Dependent β-Thalassemia Caused by Compound Heterozygous Mutations of HBB: C.84_85insC and Common Linked Intronic Variants in HBB. (2025/11/01) ♡
- 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) ♡
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