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Thalassemia (severe form)
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Publications and studies (1521)
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. SARS-CoV-2 and dengue virus coinfection in an adult with beta-thalassaemia (trait): A case report from Bangladesh with literature review. (2021/10/01) ♡
- Association between iron deposition in splenic, hepatic and myocardial tissues assessed by T2* relaxometry technique. (2021/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Primary breast lymphoma - a case report. (2021/10/01) ♡
- Evaluation of right and left ventricular function using speckle-tracking echocardiography in thalassaemic patients. (2021/10/01) ♡
- Routine management, healthcare resource use and patient and carer-reported outcomes of patients with transfusion-dependent β-thalassaemia in the United Kingdom: A mixed methods observational study. (2021/09/08) ♡
- Survival and causes of death in 2,033 patients with non-transfusion-dependent β-thalassaemia. (2021/09/01) ♡
- Meta-analysisiAll studies on one question combined and calculated together. This is the strongest form of research that exists: a single loose study can be coincidence, dozens together much less so. The label says something about the design, not about the outcome — which can also be that something does NOT work. The Prevalence of Hypothyroidism among Patients With β-Thalassaemia: A Systematic Review and Meta-Analysis of Cross-Sectional Studies. (2021/09/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. First Report of the 3'-Untranslated Region +1506 (A>C) [NM_000518.5: c.*32A>C] mutation on the β-Globin Gene in the Indian Population. (2021/09/01) ♡
- Radiographic Features of the Maxillofacial Anomalies in Beta-Thalassaemia Major: With New View. (2021/09/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Dominant β-Thalassaemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report. (2021/09/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Perforated Duodenal Ulcer Associated with Deferasirox in a Child with β-Thalassaemia Major. (2021/09/01) ♡
- Multiplex Quantitative Real-Time Polymerase Chain Reaction and High-Resolution Melting Analysis for Identification of a Couple At-Risk of Having a Newborn with Severe Thalassaemia. (2021/09/01) ♡
- Spectrum of β-Thalassaemia Mutations in Some Areas of Guangxi Zhuang Autonomous Region of Southern China: A Study on a Pediatric Population Aged 0-15 Years. (2021/09/01) ♡
- Meta-analysisiAll studies on one question combined and calculated together. This is the strongest form of research that exists: a single loose study can be coincidence, dozens together much less so. The label says something about the design, not about the outcome — which can also be that something does NOT work. Effects of dietary polyphenol supplementation on iron status and erythropoiesis: a systematic review and meta-analysis of randomized controlled trials. (2021/08/02) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Repeated CD45RA-depleted DLI successfully increases donor chimerism in a patient with beta-thalassaemia major after haploidentical stem cell transplant. (2021/08/01) ♡
- Is CONUT score a predictor of morbidity in patients with adult transfusion dependent beta thalassaemia? (2021/08/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. SARS-CoV-2 infection in patients with β-thalassaemia: Experience from Lebanon. (2021/08/01) ♡
- Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassaemia mutations. (2021/08/01) ♡
- Detection of endocrine disorders in young children with multi-transfused thalassaemia major. (2021/07/31) ♡
- Alpha-globin gene triplication and its effect in beta-thalassaemia carrier, sickle cell trait, and healthy individual. (2021/07/19) ♡
- Vitamin C Deficiency and Oxidant Levels in Children With Transfusion-Dependent β-Thalassaemia. (2021/07/15) ♡
- NESTROFT-A Cost-Effective Mass Screening Tool for the Detection of β-Thalassaemia Carrier Status in Anaemic Pregnant Women: A Step Toward Reducing the National Disease Burden. (2021/07/09) ♡
- 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. Erythroferrone structure, function, and physiology: Iron homeostasis and beyond. (2021/07/01) ♡
- Prenatal Screening and Diagnosis of β-Thalassaemia in India: Is ARMS-PCR Enough? (2021/07/01) ♡
- Role of Red Cell Indices in Screening for Beta Thalassaemia Trait: an Assessment of the Individual Indices and Application of Machine Learning Algorithm. (2021/07/01) ♡
- A Retrospective Long-Term Study on Age at Menarche and Menstrual Characteristics in 85 Young Women with Transfusion-Dependent β-Thalassaemia (TDT). (2021/07/01) ♡
- Updated Molecular Spectrum of β-Thalassaemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration. (2021/07/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Hb Jishui [HBA1: c.225C>G, Codon 74 (GAC>GAG), Asp→Glu]: A Novel α Chain Haemoglobin Variant Detected During Hb A(1c) Measurement. (2021/07/01) ♡
- 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. Borderline HbA(2) levels: Dilemma in diagnosis of beta-thalassaemia carriers. (2021/07/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A successful booster umbilical cord blood transplantation for a 10-year-old patient with beta-thalassaemia major in India. (2021/07/01) ♡
- Estimation of prevalence of red cell alloantibodies in patients with Beta Thalassaemia Major in Sri Lanka. (2021/06/30) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Drug utilisation study and cost analysis of adult β-thalassaemia major patient therapy at Dr. Soetomo General Hospital Surabaya. (2021/06/25) ♡
- β-Haemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program. (2021/06/01) ♡
- Further evaluation of the world health organization international reference reagent for Haemoglobin A(2) measurement. (2021/06/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Spectrum of pathogenic alterations identified after two decades of HBB gene sequencing for molecular diagnosis of beta-thalassaemias and haemoglobinopathies. (2021/06/01) ♡
- 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. Vitamin D and bone health status in beta thalassemia patients-systematic review. (2021/06/01) ♡
- 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. Effects of alpha lipoic acid on iron overload, lipid profile and oxidative stress indices in β-thalassemia major patients: A cross-over randomised controlled clinical trial. (2021/06/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Abnormal hemoglobin H band in myelodysplastic syndromes (MDS): A case report. (2021/05/01) ♡
- Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at (G)γ-globin gene promoter. (2021/04/20) ♡
- 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 using haematopoietic stem and progenitor cells. (2021/04/01) ♡
- MicroRNA-2355-5p regulates γ-globin expression in human erythroid cells by inhibiting KLF6. (2021/04/01) ♡
- Discriminant Indices for Screening Beta Thalassemia Trait: An Illusion of Choice. (2021/04/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Changes in Liver Stiffness and Noninvasive Fibrosis Scores in Egyptian Adolescents Successfully Treated with Ledipasvir-Sofosbuvir for Chronic Hepatitis C Virus Infection. (2021/04/01) ♡
- 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. Curcuminoids supplementation ameliorates iron overload, oxidative stress, hypercoagulability, and inflammation in non-transfusion-dependent β-thalassemia/Hb E patients. (2021/04/01) ♡
- Addressing the psychosocial needs of young people with thalassaemia undergoing bone marrow transplantation. (2021/03/04) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Management of non-transfusion-dependent β-thalassemia (NTDT): The next 5 years. (2021/03/01) ♡
- MicroRNA expression patterns in HbE/β-thalassemia patients: The passwords to unlock fetal hemoglobin expression in β-hemoglobinopathies. (2021/03/01) ♡
- 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. Effects of three months of treatment with vitamin E and N-acetyl cysteine on the oxidative balance in patients with transfusion-dependent β-thalassemia. (2021/03/01) ♡
- Genome-wide analysis of pseudogenes reveals HBBP1's human-specific essentiality in erythropoiesis and implication in β-thalassemia. (2021/02/22) ♡
- 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. Erythroblastic Island Macrophages Shape Normal Erythropoiesis and Drive Associated Disorders in Erythroid Hematopoietic Diseases. (2021/02/12) ♡
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