Disease: Beta-thalassemia
- A cross-sectional study: caregiver burden and related determinants of adult patients with beta-thalassemia major in mainland China
- A Novel 165 Kb Duplication Involving the alpha-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient
- A Novel Frameshift Mutation(HBA2:C.337delC) Associated With alpha-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China
- A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With beta-Thalassemia
- A scoping review exploring cure definitions and language for inherited hemoglobinopathies
- Abnormal hemoglobin anti-Lepore Hong Kong compound with beta(0)-thalassemia ameliorate thalassemia severity when co-inherited with alpha-thalassemia
- Acute Graft versus Host Disease in Beta Thalassemia Patients Following Allogeneic Haematopoietic Stem Cell Transplantation
- Advance of research on the role of BCL11A in the occurrence and treatment of beta-Thalassemia
- Ancestral beta-globin gene haplotypes modify beta-thalassemia severity in a mouse model
- Artificial intelligence-driven diagnosis of beta-thalassemia minor & iron deficiency anemia using machine learning models
- Autologous Gene Therapy for Hemoglobinopathies: From Bench to Patient's Bedside
- beta(0)-Thalassemia Caused by a Novel Nonsense Mutation [HBB:c.199A > T]
- Beyond the promise: evaluating and mitigating off-target effects in CRISPR gene editing for safer therapeutics
- Bile Acid-Targeted Hyaluronic Acid Nanoparticles for Enhanced Oral Absorption of Deferoxamine
- Birth Prevalence of Sickle Cell Disease and County-Level Social Vulnerability - Sickle Cell Data Collection Program, 11 States, 2016-2020
- Bone Health Impairment in Patients with Hemoglobinopathies: From Biological Bases to New Possible Therapeutic Strategies
- Bone marrow Tfr2 deletion improves the therapeutic efficacy of the activin-receptor ligand trap RAP-536 in beta-thalassemic mice
- Can Cyprus Afford Luspatercept? A Budget Impact Analysis of the Reimbursement of Luspatercept for the Management of Thalassaemia in Cyprus
- Cas9 RNP Physiochemical Analysis for Enhanced CRISPR-AuNP Assembly and Function
- Clinical Analysis of Children with Thalassemia in Chongqing
- Cognitive impairment and hippocampal neuronal damage in beta-thalassaemia mice
- Combination of a TGF-beta ligand trap (RAP-GRL) and TMPRSS6-ASO is superior for correcting beta-thalassemia
- Compound heterozygosity for Southeast Asian hereditary persistence of fetal hemoglobin and beta0-thalassemia results in thalassemia intermedia: Pedigree analysis and genetic research in a family from South China. A case report
- Concurrent Challenges in Idiopathic Hypereosinophilic Syndrome Complicating Beta-Thalassemia Major: A Case Report
- Deferasirox: A comprehensive drug profile
- Deferiprone-resveratrol hybrid attenuates iron accumulation, oxidative stress, and antioxidant defenses in iron-loaded human Huh7 hepatic cells
- Detection of CRISPR/Cas9-Mediated Fetal Hemoglobin Reactivation in Erythroblasts Derived from Cord Blood-Hematopoietic Stem Cells
- Development and Psychometric Assessment of "Self-Efficacy Scale" for Patients With Beta Thalassemia Major: A Mixed-Methods Study
- Development of pathophysiologically relevant models of sickle cell disease and beta-thalassemia for therapeutic studies
- Droplet digital polymerase chain reaction-based quantitation of therapeutic lentiviral vector copies in transduced hematopoietic stem cells
- Editorial for "Marrow Fat-Cortical Bone Relationship in beta-Thalassemia: A Study Using MRI"
- Editorial: First Regulatory Approvals for CRISPR-Cas9 Therapeutic Gene Editing for Sickle Cell Disease and Transfusion-Dependent beta-Thalassemia
- Effects of multidisciplinary team continuous care model on psychological behavior and quality of life in children with beta-thalassemia major
- Evaluation of some nonroutine cardiac biomarkers among adults and children with beta-thalassemia major
- Exagamglogene Autotemcel for Transfusion-Dependent beta-Thalassemia
- Ginsenoside Rg1 promotes fetal hemoglobin production in vitro: A potential therapeutic avenue for beta-thalassemia
- Growth and endocrinopathies among children with beta-Thalassemia major treated at Dubai Thalassemia centre
- Haemoglobin Bart's Hydrops Fetalis: Charting the Past and Envisioning the Future
- HbA1c or fructosamine on evaluating glucose intolerance in children with beta- thalassemia
- Health status and quality of life in beta-thalassemia adults in Marseille, France
- Health-Related Quality-of-Life Impacts Associated with Transfusion-Dependent beta-Thalassemia in the USA and UK: A Qualitative Assessment
- Hearing loss in beta-thalassaemia: An Italian multicentre case-control study
- Higher hemoglobin is better in thalassemia
- Hospital-acquired pneumonia due to Burkholderia cepacia in a thalassemia pregnancy with postoperative eclampsia: A case report
- Impact of alpha-Globin Gene Expression and alpha-Globin Modifiers on the Phenotype of beta-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management
- Impact of COVID-19 on patients with beta-thalassemia major: an observational study
- Impact of genotype on multi-organ iron and complications in patients with non-transfusion-dependent beta-thalassemia intermedia
- Impact of SCOPE Program on Health-Related Quality of Life and Health Status of Children With Thalassemia: A Quasi-Experimental Study
- In brief: Casgevy for beta thalassemia
- Left atrial strain in patients with beta-thalassemia major: a cross-sectional CMR study
- Letter to the Editor: Impacts of beta-thalassemia/hemoglobin E disease on pregnancy outcomes
- Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation
- Luspatercept in low-risk myelodysplastic syndromes: a paradigm shift in treatment strategies
- Magnitude of Bone Disease in Transfusion-Dependent and Non-Transfusion-Dependent beta-Thalassemia Patients
- Marrow Fat-Cortical Bone Relationship in beta-Thalassemia: A Study Using MRI
- miR-214 aggravates oxidative stress in thalassemic erythroid cells by targeting ATF4
- Molecular Characterization of alpha- and beta-Thalassemia Among Children Less Than 18 Years Old in Guizhou, China
- Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing
- Molecular epidemiology and hematological profiles of hemoglobin variants in southern Thailand
- Multiparametric Cardiac Magnetic Resonance Assessment in Sickle Beta Thalassemia
- Multiparametric cardiac magnetic resonance in patients with thalassemia intermedia: new insights from the E-MIOT network
- National Quality Indicators in Pediatric Sickle Cell Anemia
- Natural Anticoagulant Protein Levels in Patients With Beta-Thalassemia Major: A Case-Control Study
- Newborn Screening for beta-Thalassemia Identifies a Complex Genotype Involving a Novel beta-Globin Gene Mutation (HBB:c.336dup)
- Optimizing lentiviral genomic integrations to cure beta-thalassemia: The least required for success?
- Outcomes of Haematopoietic Stem Cell Transplantation in Beta Thalassemia Major with Fully Matched Parents as Donor
- Oxidative Stress and Antioxidant Status in Adult Patients with Transfusion-Dependent Thalassemia: Correlation with Demographic, Laboratory, and Clinical Biomarkers
- Pancreatic iron in pediatric transfusion-dependent beta-thalassemia patients: A longitudinal MRI study
- Pharmacogenomics of Drugs Used in beta-Thalassemia and Sickle-Cell Disease: From Basic Research to Clinical Applications
- Point Shear Wave Elastography Detected Liver Stiffness Increased in Pediatric Patient With Thalassemia Major
- Point-of-Care Diagnostic Test for Beta-Thalassemia
- Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq
- Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening
- Prevalence of thalassemia-carrier couples and fertility risk assessment
- Prognostic Role of Multiparametric Cardiac Magnetic Resonance in Neo Transfusion-Dependent Thalassemia
- Proportion of Hypogonadism in Transfusion-Dependent Thalassemia Patients and Its Contributing Factors
- Proteomic profiling of circulating beta-thalassaemia/haemoglobin E extra-cellular vesicles reveals that association with immunoglobulin induces membrane vesiculation
- Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis
- Reticulocyte Antioxidant Enzymes mRNA Levels versus Reticulocyte Maturity Indices in Hereditary Spherocytosis, beta-Thalassemia and Sickle Cell Disease
- Revisiting iron overload status and change thresholds as predictors of mortality in transfusion-dependent beta-thalassemia: a 10-year cohort study
- RNA therapeutics for beta-thalassemia
- Screening and Diagnosis of Rare Thalassemia Variants
- Screening for thalassemia carriers among the Han population of childbearing age in Southwestern of China
- Secondary amenorrhea in a beta-thalassemia major patient treated with thalidomide
- Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two alpha-Globin Gene Defects, Hb Taybe D HBA1: C.119_121delCCA Mutation and HBA2: C.*94A > G Mutation
- Sickle cell disease and increased adverse maternal and perinatal outcomes in different genotypes
- Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with beta-thalassemia
- Spectrum of Rare and Novel Indel Mutations Responsible for beta Thalassemia in Eastern India
- Study of the types of mutations of Thalassemia in Shanghai area
- Survival and causes of death in patients with alpha and beta-thalassemia in Northern Thailand
- Systematic Review and Meta-Analysis of Health-Related Quality of Life in Patients with beta-Thalassemia that Underwent Hematopoietic Stem Cell Transplantation
- The Evaluation of Invasive Prenatal Diagnostic Tests in North Cyprus: A Retrospective Study
- The interactions between ineffective erythropoiesis and ferroptosis in beta-thalassemia
- The Italian breakthrough in CRISPR trials for rare diseases: a focus on beta-thalassemia and sickle cell disease treatment
- Unplanned pregnancy in women with beta-thalassaemia treated with luspatercept
- Unraveling a Rare Case of Epidural Extramedullary Hematopoiesis in a Patient With Transfusion-Dependent Beta Thalassemia Presenting With Spinal Cord Compression
- Unravelling the Complexity of the +33 C>G [HBB:c.-18C>G] Variant in Beta Thalassemia
- Urethral meatus edema with peno-scrotal edema in a patient with transfusion-dependent beta-thalassemia major
- Very low serum IGF-1 levels are associated with vertebral fractures in adult males with beta-thalassemia major
- Viral Vectors in Gene Replacement Therapy