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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. HBB mutations and HbA2 level: Escaping the carrier screening programs. (2020/12/29) ♡
- Discovery of DS79932728: A Potent, Orally Available G9a/GLP Inhibitor for Treating β-Thalassemia and Sickle Cell Disease. (2020/12/28) ♡
- Choroidal Thickness Evaluation in a Transfusion-Dependent Beta-Thalassemia Greek Population. (2020/12/24) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. The Dilemma of Diagnosing Hemophagocytic Lymphohistiocytosis in Sickle Cell Disease. (2020/12/24) ♡
- Left Atrial Strain Identifies Increased Atrial Ectopy in Patients with Beta-Thalassemia Major. (2020/12/22) ♡
- Gene Therapy for Monogenic Inherited Disorders. (2020/12/21) ♡
- 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 COVID-19 reinfection in a patient with beta thalassemia major. (2020/12/19) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Denosumab versus zoledronic acid for patients with beta-thalassemia major-induced osteoporosis. (2020/12/18) ♡
- Oral Health Profiles and Related Quality of Life in Thalassemia Children in Relation to Iron Overload: A Cross-Sectional Study. (2020/12/16) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Spinal cord compression due to extramedullary hematopoiesis in patient with Beta thalassemia major. (2020/12/15) ♡
- Time to Start Delivering Iron Chelation Therapy in Newly Diagnosed Severe β-Thalassemia. (2020/12/13) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Incidental Diagnosis of Adult Beta-Thalassemia With Point-of-Care Ultrasound in the Emergency Department: A Case Report. (2020/12/13) ♡
- Evaluation of myocardial perfusion and function in patients with asymptomatic beta-thalassemia major using myocardial gated single-photon-emission computed tomography. (2020/12/12) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Tweaking genes with CRISPR or viruses fixes blood disorders. (2020/12/11) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Prominent pseudo-Gaucher cells in a patient with β-thalassemia intermedia and plasma cell myeloma. (2020/12/10) ♡
- Doppler-defined pulmonary hypertension in β-thalassemia major in Kurdistan, Iraq. (2020/12/10) ♡
- [Study of the genotypic and hematological feature of hemoglobin H disease in West Guangxi area]. (2020/12/10) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. [Diagnosis and clinical phenotype analysis of a case with large fragment homozygous deletion of rare β gene cluster]. (2020/12/10) ♡
- Molecular Characterization and Disease-Related Morbidities of β-Thalassemia Patients from the Northeastern Part of Iraq. (2020/12/09) ♡
- Access to health care for patients with thalassaemia in Greece: a cross-sectional study. (2020/12/09) ♡
- 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. Challenges in chronic transfusion for patients with thalassemia. (2020/12/04) ♡
- 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. Human Leukocyte Antigen Complex and Other Immunogenetic and Clinical Factors Influence Susceptibility or Protection to SARS-CoV-2 Infection and Severity of the Disease Course. The Sardinian Experience. (2020/12/04) ♡
- DNA methylation patterns of β-globin cluster in β-thalassemia patients. (2020/12/03) ♡
- Moderate to severe liver siderosis and raised AST are independent risk factors for vitamin D insufficiency in β-thalassemia patients. (2020/12/03) ♡
- A study of red blood cell alloimmunization and autoimmunization among 200 multitransfused Egyptian β thalassemia patients. (2020/12/03) ♡
- 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. β-Hemoglobinopathies: The Test Bench for Genome Editing-Based Therapeutic Strategies. (2020/12/03) ♡
- 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 literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients. (2020/12/02) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Serum folate and cytokines in heterozygous β-thalassemia. (2020/12/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene. (2020/12/01) ♡
- Relation of hepcidin gene expression in blood mononuclear cells with iron overload severity among β-thalassemia major patients. (2020/12/01) ♡
- [Analysis of Gene Mutation Types of Thalassemia in Yulin Childbearing-age Population of Guangxi China]. (2020/12/01) ♡
- [Analysis and Prevention of Gene Mutation Types of Severe Thalassemia in Hakka People in Gannan of Jiangxi Province]. (2020/12/01) ♡
- [Clinical Features of Pregnant Women with Thalassemia in Non Endemic Area]. (2020/12/01) ♡
- [Hematological Analysis and Diagnosis of Two Rare Abnormal Hemoglobin]. (2020/12/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. CRISPR gene therapy shows promise against blood diseases. (2020/12/01) ♡
- Hemoglobin Disorders Among Anemic Patients: a Cross-Sectional Study from Jeddah City, Western Saudi Arabia. (2020/12/01) ♡
- Clinical impacts of DNA-based typing and provision of antigen-matched red blood cell units for chronically transfused patients with thalassemia. (2020/12/01) ♡
- Hematopoietic Stem Cell Transplantation in Thalassemia Patients: a Jordanian Single Centre Experience. (2020/12/01) ♡
- The Frequency of Beta-Thalassemia Mutations among Carriers in Dezful City, Southwest Iran. (2020/12/01) ♡
- 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. Management of Iron Overload in Beta-Thalassemia Patients: Clinical Practice Update Based on Case Series. (2020/11/20) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Polycythemia Vera in a Patient With Heterozygous Beta-Thalassemia: Coincidence or Causal Relationship? (2020/11/20) ♡
- Impact of activated monocyte and endothelial dysfunction on coagulopathy in Egyptian adult beta thalassemic patients. (2020/11/17) ♡
- Depression, Anxiety, and Stress Symptoms in Patients With Beta Thalassemia Major in Almadinah Almunawwarah, Saudi Arabia. (2020/11/07) ♡
- 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. Cardiac T(2) * mapping: Techniques and clinical applications. (2020/11/01) ♡
- High Prevalence of Anemia and Inherited Hemoglobin Disorders in Tribal Populations of Madhya Pradesh State, India. (2020/11/01) ♡
- Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, HBB: c.[79G>A;198G>C]): A Novel β-Thalassemic Hemoglobin Variant. (2020/11/01) ♡
- Six-year experience of prenatal diagnosis for beta thalassemia in twin pregnancies and selective foetal reduction - A case series. (2020/11/01) ♡
- 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. Calcium Channel Blockers in Conjunction with Standard Iron-Chelating Agents for β-Thalassemia Major: Systematic Literature Search. (2020/11/01) ♡
- Nature and severity of dental malocclusion in children suffering from transfusion-dependent β-thalassemia major. (2020/11/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Septicemic melioidosis complicating undiagnosed chronic kidney disease and beta-thalassemia minor in a Bangladeshi farmer. (2020/11/01) ♡
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