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Thalassemia (severe form)

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Search Period All yearsLast 12 monthsLast 5 years Topic All topicsGeneralNutrition and dietAlternative treatment methods Type of research Any type of researchOnly the strongest evidence (53)Meta-analysis (12)Treatment guideline (1)Randomized trial (20)Systematic review (12)Phase 3 study (8)Clinical trial (379)Review article (138)Early study (phase 1 or 2) (18)Case report (134)Laboratory or animal research (17)Commentary or editorial (44)Retracted publication (2) Studies currently recruiting participants only (31)

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Publications and studies (1521)

• Iron chelators or therapeutic modulators of iron overload: Are we anywhere near ideal one? (2018/10/01) ♡
• A Comparison Of Skeletal Age Of Thalassaemic Patients Of 9-15 Years With Chronological Age By Radiography. (2018/10/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Pre- and Post-transfusion Complement Activation in Transfusion-dependent β-thalassaemia. (2018/10/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An unusual case of a posterior mediastinal myelolipoma in a patient with mediterranean anemia. (2018/09/27) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Unexpected discovery of hemoglobinopathy C/β° thalassemia. (2018/09/21) ♡
• The Spectrum of Beta-thalassemia Mutations in Couples Referred for Chorionic Villus Sampling at Bahawal Victoria Hospital, Bahawalpur. (2018/09/07) ♡
• 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. An investigation of the effects of curcumin on iron overload, hepcidin level, and liver function in β-thalassemia major patients: A double-blind randomized controlled clinical trial. (2018/09/01) ♡
• The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature. (2018/09/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Hb Sichuan [α67(E16)Thr→Ile, HBA2: c.203C>T]: A Novel Hemoglobin Variant That Can Be Detected by Glycated Hemoglobin Electrophoresis. (2018/09/01) ♡
• Results of Coexistence of β-Thalassemia Minor in Hb H Disease Patients. (2018/09/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement Inhibition. (2018/09/01) ♡
• β-Thalassemia Mutations in Jamaica: Geographic Variation in Small Communities. (2018/09/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Rare Association of Hb D-Los Angeles (HBB: c.364G>C) with Hb H Disease: Diagnosis and Clinical Implications. (2018/09/01) ♡
• Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India. (2018/09/01) ♡
• Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients. (2018/09/01) ♡
• Quality of Life and Depression in Turkish Patients with β-Thalassemia Major: A Cross-Sectional Study. (2018/09/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Quality of Life of Pakistani Children with β-Thalassemia Major. (2018/09/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Coinheritance of HbD-Punjab/β+-thalassemia (IVSI+5 G-C) in patient with Gilbert's syndrome. (2018/08/17) ♡
• Blood transfusion versus hydroxyurea in beta-thalassemia in Iran: a cost-effectiveness study. (2018/08/01) ♡
• Modulation of hepcidin expression by normal control and beta0-thalassemia/Hb E erythroblasts. (2018/08/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Deferoxamine-induced electronegative ERG responses. (2018/08/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Echocardiographic evaluation of prevalence of pulmonary hypertension in β-thalassemia major: A cross sectional study. (2018/08/01) ♡
• Comparative evaluation of oral and dento-maxillofacial manifestation of patients with sickle cell diseases and beta thalassemia major. (2018/07/01) ♡
• Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western India. (2018/07/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Codon 14 (+T) (HBB: c.44_45insT): a Rare β-Thalassemia Mutation Reported Only in Azerbaijan. (2018/07/01) ♡
• Frequency of α-Globin Gene Triplications and Coinheritance with β-Globin Gene Mutations in the Iranian Population. (2018/07/01) ♡
• 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 Rare Hb H Hydrops Fetalis Syndrome Caused by the - -(SEA) Deletion in Combination with the Rare Hb Hirosaki Mutation in a Chinese Patient. (2018/07/01) ♡
• Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia. (2018/07/01) ♡
• Relationship Between Social Determinants of Health and the Thalassemia Prenatal Diagnosis Test in Zahedan, South Eastern Iran. (2018/07/01) ♡
• First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family. (2018/07/01) ♡
• Experience of hepatitis C virus seroprevalence and its genomic diversity among transfusion-dependent thalassemia patients in a transfusion center. (2018/07/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Manual red cell exchange transfusion to avert sickle cell related complications. (2018/07/01) ♡
• BCL11A Down-Regulation Induces γ-Globin in Human β-Thalassemia Major Erythroid Cells. (2018/07/01) ♡
• Haplotype Analysis of β-Thalassaemia Major and Carriers with Filipino β°-Deletion in Sabah, Malaysia. (2018/07/01) ♡
• 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. Pharmacological and molecular approaches for the treatment of β-hemoglobin disorders. (2018/06/01) ♡
• Effects of the iron chelator deferiprone and the T-type calcium channel blocker efonidipine on cardiac function and Ca(2+) regulation in iron-overloaded thalassemic mice. (2018/06/01) ♡
• Correlation of Ultra-Widefield Fluorescein Angiography and OCT Angiography in Sickle Cell Retinopathy. (2018/06/01) ♡
• Clinico-hematological Profile of Hb E-β Thalassemia-Prospective Analysis in a tertiary Care Centre. (2018/06/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Hepatitis E with Intravascular Hemolysis in Beta Thalassemia Trait: A Rare Association or Coincidence. (2018/06/01) ♡
• Role of CYP24A1, VDR and GC gene polymorphisms on deferasirox pharmacokinetics and clinical outcomes. (2018/05/22) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Epsilon gamma delta beta thalassemia: A rare cause of fetal and neonatal anemia. (2018/05/11) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Acute Splenic Sequestration Crisis After Red Blood Cell Exchange for Acute Chest Syndrome in an Adult With Sickle β-Thalassemia: What Went Wrong? (2018/04/01) ♡
• 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. Ineffective Erythropoiesis: Anemia and Iron Overload. (2018/04/01) ♡
• 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. Hypercoagulability and Vascular Disease. (2018/04/01) ♡
• 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. Emerging Therapies. (2018/04/01) ♡
• Clinico-Hematological Profile of Hb Q India: An Uncommon Hemoglobin Variant. (2018/04/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Coinheritance of Sicilian (δβ)(0)-Thalassemia and Two Rare Hemoglobin Variants: A Complex Case of Hemoglobinopathy. (2018/04/01) ♡
• The Zinc and Copper Levels in Thalassemia Major Patients, Receiving Iron Chelation Therapy. (2018/04/01) ♡
• Mean reticulocyte hemoglobin content index plays a key role to identify children who are carriers of β-thalassemia. (2018/03/31) ♡
• Mean reticulocyte hemoglobin content index plays a key role to identify children who are carriers of β-thalassemia. (2018/03/31) ♡

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