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Blood and bone marrow
Thalassemia (severe form)
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Publications and studies (1521)
- 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. HEV Infection in Beta-Thalassemia Patients. (2024/12/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Breaking the cycle of transfusion dependence in β-thalassaemia. (2024/11/30) ♡
- The growth and development of children with β-thalassemia major one year after allogeneic hematopoietic stem cell transplantation. (2024/11/30) ♡
- Association of Serum Ferritin With Growth and Endocrine Function in Thalassemia Major Children in North India: An Observational Study. (2024/11/30) ♡
- Comparison of Efficacy and Safety Outcomes of Different Doses Schedules of Thalidomide for Treating Moderate-to-Severe β-Thalassemia Patients. (2024/11/29) ♡
- Green Tea Epigallocatechin 3-Gallate Reduced Platelet Aggregation and Improved Anticoagulant Proteins in Patients with Transfusion-Dependent β-Thalassemia: A Randomized Placebo-Controlled Clinical Trial. (2024/11/29) ♡
- In vivo silencing of intestinal DMT1 mitigates iron loading in β-thalassemia intermedia (Hbbth3/+) mice. (2024/11/26) ♡
- 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. Serum lipid profile abnormalities among beta-thalassemia patients: a systematic review and meta-analysis. (2024/11/25) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Non-HFE Hemochromatosis in the Context of β-Thalassemia Trait: A Case Study on Iron Overload Dysregulation. (2024/11/25) ♡
- Shear Wave Elastography in the Assessment of Liver Iron Overload in Children With Beta Thalassemia Major. (2024/11/22) ♡
- Automated Quantitative Assessment of Retinal Vascular Tortuosity in Patients with Sickle Cell Disease. (2024/11/22) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Homozygous Delta-Beta Thalassaemia With Alpha Thalassaemia and Erythrocytosis- a Rare Case Report. (2024/11/21) ♡
- Cardiovascular Effects of Splenomegaly and Splenectomy in Beta-Thalassemia Major. (2024/11/21) ♡
- 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. Beta Thalassemia in Children: Established Approaches, Old Issues, New Non-Curative Therapies, and Perspectives on Healing. (2024/11/19) ♡
- Comparison of the effects of deferasirox film-coated tablets (Jadenu(®)) and deferasirox dispersible tablets (Exjade(®)) in patients with beta thalassemia major: a preliminary report of the effects on the satisfaction, convenience, cardiac/liver MRI T2*, serum ferritin level, and biochemical profiles. (2024/11/19) ♡
- A glutamine metabolic switch supports erythropoiesis. (2024/11/15) ♡
- Identifying thresholds for meaningful improvements in NTDT-PRO scores to support conclusions about treatment benefit in clinical studies of patients with non-transfusion-dependent beta-thalassaemia: analysis of pooled data from a phase 2, double-blind, placebo-controlled, randomised trial. (2024/11/14) ♡
- From bacterial operons to gene therapy: 50 years of the journal Cell. (2024/11/14) ♡
- A Modular Genetic Approach to Newborn Screening from Spinal Muscular Atrophy to Sickle Cell Disease-Results from Six Years of Genetic Newborn Screening. (2024/11/13) ♡
- Genetic screening of α-thalassemia fusion gene using routine flow-through hybridization. (2024/11/12) ♡
- 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. A scoping review on the obstacles faced by beta thalassemia major patients in Pakistan- Matter of policy investment. (2024/11/12) ♡
- A particular focus on the prevalence of α-thalassemia and β-thalassemia among pregnant women in Changsha County, Hunan Province. (2024/11/07) ♡
- Estimation of HbA1c Levels in Transfusion-Dependent Thalassemia Patients in Comparison With Normal Healthy Individuals. (2024/11/07) ♡
- Genotype-phenotype correlation analysis of patients with thalassemia in quanzhou city, southeast of China. (2024/11/05) ♡
- 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 Modifiers of Hemoglobin Expression from a Clinical Perspective in Hemoglobinopathy Patients with Beta Thalassemia and Sickle Cell Disease. (2024/11/05) ♡
- Bone and Joint Involvement in Beta Thalassemic Patients: A Cross-sectional Study. (2024/11/05) ♡
- Luspatercept in β-thalassemia: Who and when. Strengths and weaknesses points of a real-world evidence. (2024/11/04) ♡
- Experiences of family caregivers of children living with thalassaemia-major in Karachi: a phenomenological study. (2024/11/02) ♡
- Ten years of a neonatal screening program for hemoglobinopathies in Friuli-Venezia Giulia: first regional experience in Italy. (2024/11/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. The Efficacy of Mitapivat in Case of Transfusion Dependence Linked to Beta Thalassemia Trait Associated with Pyruvate Kinase Deficiency. (2024/11/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Falsely Elevated HbA1c Levels in a Patient with Type 2 Diabetes Mellitus and Multiple Beta Globulin Gene Mutations. (2024/11/01) ♡
- A novel synthetic compound, deferiprone-resveratrol hybrid (DFP-RVT), promotes hepatoprotective effects and ameliorates iron-induced oxidative stress in iron-overloaded β-thalassemic mice. (2024/11/01) ♡
- Outcomes of the premarital screening program in Riyadh Region, KSA in 2021-2022: A cross-sectional study. (2024/10/29) ♡
- Investigation of Depression, Anxiety, Sleep Quality, and Fatigue in Thalassemia Major Patients: A Study of the Correlation Between Sleep Quality and Laboratory Findings. (2024/10/29) ♡
- The relationship between ghrelin and iron metabolism in beta thalassaemia major patients. (2024/10/26) ♡
- Association of age to nutritional status and muscle mass in children with transfusion-dependent β-thalassemia: a cross-sectional study. (2024/10/25) ♡
- Deferoxamine, deferasirox, and deferiprone triple iron chelator combination therapy for transfusion-dependent β-thalassaemia with very high iron overload: a randomised clinical trial. (2024/10/15) ♡
- 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. Targeted liquid biopsy for brain tumors. (2024/10/12) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. False HbA(1c) value due to a rare variant of hemoglobin Petie Salpetriere coinherited with alpha thalassemia. (2024/10/09) ♡
- HbA1c or fructosamine on evaluating glucose intolerance in children with beta-thalassemia. (2024/10/01) ♡
- 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. Exploring Novel Strategies to Alleviate Symptoms of β-Globinopathies: Examining the Potential Role of Embryonic ε-globin Induction. (2024/10/01) ♡
- A study to assess the occurrence of anaemia and beta-thalassemia in the tribal population residing in the Yadadri-Bhuvanagiri district of Telangana state. (2024/10/01) ♡
- Characterization Of Beta Thalassaemia Mutations In Patients Having Borderline Haemoglobin A2 Levels. (2024/10/01) ♡
- Vitamin D Deficiency among Blood Transfusion Dependent Beta Thalassemia Children Admitted to Tertiary Level Pediatric Hospital in Nepal: A Descriptive Cross-sectional Study. (2024/10/01) ♡
- α(0)-Thalassemia Caused by a Novel α-Globin Gene Cluster Deletion (-(LB)) Found in a Chinese Family. (2024/09/01) ♡
- 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. Burden of illness of non-hematopoietic stem cell transplant-related hepatic sinusoidal obstruction syndrome: A systematic review. (2024/08/31) ♡
- Genotype Distribution and Clinical Characteristics of Thalassemia Patients Needing Transfusion in Yangjiang, Western Guangdong. (2024/08/28) ♡
- 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. Acute Pancreatitis in Individuals with Sickle Cell Disease: A Systematic Review. (2024/08/11) ♡
- Assessment of Serum Vitamin D and Parathyroid Hormone in Children With Beta Thalassemia Major: A Case-Control Study. (2024/08/04) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Comparison of Yearly Cost Related to Complications Between Deferasirox and Deferiprone Monotherapy in Thalassemia. (2024/08/01) ♡
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