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What researchers published on Thalassaemia

1,090 papers, newest first.

Showing 160 of 1,090

  • Not labelled yetAssociation of HBB gene variants with cardiometabolic and renal phenotypes in a Taiwanese genomic cohort: a cross-sectional study.BMC genomics
  • Not labelled yetDemographic and Nutritional Profile of Thalassemia Carrier and Non-Carrier Young Children in Bangladesh: A Comparative Study.Food science & nutrition
  • Not labelled yetATRX deficiency drives aberrant type I interferon signalling through cGAS-dependent transcriptional dysregulation.Nature communications
  • Not labelled yetEvaluation of the Efficacy and Safety of Alternating Chelation Therapy in Transfusion-Dependent Thalassemia.Hemoglobin
  • Not labelled yetSelf-management experiences of individuals with β-thalassemia major: a hermeneutic phenomenological study.Irish journal of medical science
  • Not labelled yetCost-effectiveness and cost-benefit analysis of the thalassaemia prevention programme in Guangdong, southern China.Preventive medicine reports
  • Not labelled yetErratum: A predictive model for low bone mass in pediatric and adolescent patients with transfusion-dependent beta-thalassemia.Translational pediatrics
  • Case reportCase Report: Low-dose donor lymphocyte infusion for secondary poor graft function after haploidentical HSCT in a child with β-thalassemia.Frontiers in immunology
  • Case reportIncidental STR profiling during thalassemia screening rescues a normal male fetus from Turner syndrome misdiagnosis following chorionic villus sampling.Clinica chimica acta; international journal of clinical chemistry
  • PreprintClinGen Hemoglobinopathy VCEP ACMG/AMP specifications for HBB and HBA2 variant interpretation in thalassemia.medRxiv : the preprint server for health sciences
  • Not labelled yetMolecular Reclassification Versus Misdiagnosis in α-Thalassemia.International journal of laboratory hematology
  • Not labelled yetComments on "surface-based brain age index reflects hematological impacts on cognitive development in children with beta-thalassemia major".iScience
  • Not labelled yetPersistent Hypereosinophilia in Adrenal Insufficiency in Transfusion-Dependent β-Thalassaemia.Indian journal of pediatrics
  • Not labelled yetColorimetric detection of SEA-type α-thalassemia via hairpin-mediated EXPAR and G-quadruplex self-assembly in clinical patients.Chemical communications (Cambridge, England)
  • Not labelled yetProbable Deferasirox-Associated Acute-on-Chronic Liver Failure in Non-Transfusion-Dependent β-Thalassemia with Iron-Related Cirrhosis: A Case Report.Hemoglobin
  • Not labelled yetOcular Abnormalities in Multi-transfused Patients with Beta-thalassemia: A Cross-sectional Study from South India.Annals of African medicine
  • Not labelled yetSingle-molecule real-time (SMRT) sequencing technology shows advantages in the clinical diagnosis of complex thalassemia.Frontiers in medicine
  • Systematic reviewGenotypic-Phenotypic Correlations in Non-HbE β-Thalassemia Intermedia: A Geographic Systematic Review.Molecular genetics & genomic medicine
  • Not labelled yetCharacterization of a Novel, Recurrent 40.6 kb α0-Thalassemia Deletion in Canadians of East Indian Descent.International journal of laboratory hematology
  • Case reportImpact of luspatercept in beta-thalassemia major with alloimmunization: A case report.Therapeutic advances in hematology
  • Observational studyDental maturity and overall dental health status in children with β-thalassemia major: a case-control study.BMC oral health
  • Not labelled yetFrequency of Endocrinological Complications in Children with Thalassemia Major and Their Relationship with Ferritin Levels.Turkish archives of pediatrics
  • Not labelled yetAssociation of EPHX2 rs751141 and MIF rs755622 gene polymorphisms with cardiac complications in pediatric patients with transfusion-dependent thalassemia.Journal of immunoassay & immunochemistry
  • Not labelled yetGenotype distribution and identification of rare variants in α/β-thalassemia in chengdu: including the first report of HBA1:c.300+48C > G.Frontiers in genetics
  • Not labelled yetPublisher Correction: Thalassaemia.Nature reviews. Disease primers
  • Not labelled yetAffordable cure within reach for thalassemia.Blood advances
  • Case reportMembranous obliterans bronchitis after hematopoietic stem cell transplantation: case report.BMC pulmonary medicine
  • Case reportAdsorption-elution: Revisiting an age-old technique for identifying multiple alloantibodies and ensuring safe transfusion in a pregnant patient with HbE-beta-thalassemia.Asian journal of transfusion science
  • Not labelled yetA Canadian population-based observational cohort study of alpha and beta-thalassemia syndromes in pregnancy.Acta haematologica
  • Not labelled yetThe relationship between caregiver burden and psychological resilience among parents of children with transfusion-dependent thalassemia: A cross-sectional study.Journal of pediatric nursing
  • Not labelled yetCitrullinemia Type I Accompanied by Beta-Thalassemia Intermedia: Incidental Coexistence.Turkish journal of haematology : official journal of Turkish Society of Haematology
  • Not labelled yetGenetic and Clinical Characteristics of Thalassemia Trait and Construction of LASSO-Based Model for Its Differentiating From Iron Deficiency Anemia in Northern China.Journal of clinical laboratory analysis
  • Not labelled yetMachine Learning-Based Multiclass Classification of Hb E Carrier Status and Thalassemia-Related Hematological Profiles Using Routine Complete Blood Count Parameters.Bioengineering (Basel, Switzerland)
  • Not labelled yetSleep Patterns Across the Transfusion Cycle in Children with Transfusion-Dependent β-Thalassemia: A 14-Day Prospective Controlled Study Using Sleep Diaries and Repeated Questionnaires.Children (Basel, Switzerland)
  • Not labelled yetSerum β2-microglobulin as a marker of renal tubular damage in transfusion-dependent β-thalassemia.Caspian journal of internal medicine
  • Not labelled yetAn OR-logic-gated polarity-switching biosensor for multiplexed dual-mode thalassemia screening.Biosensors & bioelectronics
  • Not labelled yetWhen prevention constrains cure: Institutional lock-in and gene therapy access for beta-thalassemia.Social science & medicine (1982)
  • Not labelled yetRegional brain iron deposition and functional alterations in thalassemia: a multimodal human study with murine validation.Annals of hematology
  • ReviewThe epidemiology of thalassaemia syndromes in Southeast Asia.The Lancet regional health. Southeast Asia
  • Not labelled yetCorrelation Between Serum Ferritin and Electrocardiographic and Echocardiographic Markers of Cardiac Dysfunction in Children With Transfusion-Dependent β-Thalassemia Major.Cureus
  • Not labelled yetLongevity in Thalassemia: Which Clock Are We Trying to Slow?American journal of hematology
  • Not labelled yetEfficacy of Vitamin D Supplementation in Children with Transfusion Dependent Thalassemia.Indian journal of pediatrics
  • ReviewThalassaemia prevention in Asia: progress, challenges, and future directions.The Lancet regional health. Southeast Asia
  • Not labelled yetGrowth Profile and Endocrine Dysfunction in Children Aged 2-10 Years With Transfusion-Dependent β-Thalassemia Major.Cureus
  • Not labelled yetFeasibility of a Model-based HbA2 Prediction for Low-cost Screening of β-thalassemia Trait Using Blood-derived Indices: Opportunities and Challenges.The Journal of the Association of Physicians of India
  • Not labelled yetAnalysis of the diagnostic efficacy of hemoglobin capillary electrophoresis for thalassemia in children under 2 years old in Southern Fujian (Minnan) Region, China.Annals of hematology
  • Not labelled yetAutologous gene therapy versus allogeneic transplantation for sickle cell disease and transfusion-dependent β-thalassemia: Choosing between 2 definitive therapies.Seminars in hematology
  • ReviewNeurocognitive, School-Based, and Quality of Life Outcomes for Youth With Sickle Cell Disease and Thalassemia: A Scoping Review.Pediatric blood & cancer
  • Not labelled yet"A long bristling road full of adventure, full of discovery" gene therapy approaches in transfusion-dependent thalassemia: The EHA-EBMT consensus paper.HemaSphere
  • Not labelled yetThaCoder: an explainable deep learning framework for thalassemia screening using routine complete blood count: a multi-center validation study.Clinica chimica acta; international journal of clinical chemistry
  • Not labelled yetScreening for beta thalassemia trait in a heterogeneous university-based population in Delhi-NCR, India.Journal of community genetics
  • Not labelled yetAssessment of Body Mass Index (BMI) in Patients With Beta Thalassemia Major (β-TM): A Hospital-Based Study.Cureus
  • Not labelled yetA Retrospective Study of Prenatal Diagnosis for Thalassemia in 58,891 Couples from Guangxi.Fetal diagnosis and therapy
  • Not labelled yetAn integrated microfluidic sample-to-answer system for automated detection of common deletional α-thalassemia mutations.Analytica chimica acta
  • Not labelled yetPrevalence and clinical significance of α-globin gene subtypes in prenatal thalassemia screening: a focus on the -α 3.7III variant in Sanya, Hainan, China.Frontiers in pediatrics
  • Not labelled yetHaematological changes after tonsillectomy in mild thalassemia children recommendations.Brazilian journal of otorhinolaryngology
  • Not labelled yetLiving With Transfusion-Dependent Thalassemia: Adolescents' Journey Toward Normalcy-A Phenomenological Study.Journal of pediatric hematology/oncology nursing
  • Not labelled yetThe Impact of a Spiritual Care Program on the Spiritual Health of Patients with Thalassemia Major: A Clinical Trial.Iranian journal of nursing and midwifery research
  • Not labelled yetBibliometric analysis of the research trends of thalassemia in the past decade.Expert review of hematology
  • Case reportChild With β-Thalassemia Major Born Following Hematopoietic Stem Cell Transplantation in the Mother: A Case Supporting the Expansion of Genetic Counseling Services in Lebanon and the Middle East.Journal of genetic counseling
  • Not labelled yetDevelopment of loop-mediated isothermal amplification (LAMP) combined with a lateral flow dipstick DNA biosensor for detection of α thalassemia 1 [Southeast Asia (SEA), --SEA deletion].PloS one
  • Not labelled yetUnmasking Osteonecrosis: A Hidden Complication of Transfusion-Dependent β-Thalassemia Major: A Case Report.QJM : monthly journal of the Association of Physicians
  • ReviewRecent trends and innovative strategies in the curative approach for β-thalassemia: a current prospect and future perspective.Molecular biology reports
  • Case reportSF3B1-mutated MDS coexisting with β-thalassemia trait: A case report and literature review focused on diagnostic distinction from acquired β-thalassemia.Medicine
  • Not labelled yetEndocrine dysfunctions in patients with beta thalassemia major: a single-center retrospective study from Basrah.F1000Research
  • Not labelled yetCord blood-based neonatal genetic screening for thalassemia in Guiyang, China (2015): a cross-sectional study.Frontiers in genetics
  • Not labelled yetThe missing link in NET regulation after splenectomy: Splenic control on neutrophil signalling in β-thalassaemia/HbE.British journal of haematology
  • Not labelled yetNeutrophil dysregulation following splenectomy in 𝛃-thalassaemia/haemoglobin E: Myeloid homeostasis and the circulating milieu.British journal of haematology
  • Not labelled yetThe Promise and Next Steps for mHealth in Thalassemia Management.Iranian journal of medical sciences
  • ReviewThe expanding therapeutic landscape of β-thalassaemia.The Lancet. Haematology
  • ReviewFuture-proofing thalassaemia care: harnessing scalable therapies, artificial intelligence, and global collaboration.The Lancet. Haematology
  • Not labelled yetBridging the thalassaemia divide in south and southeast Asia.The Lancet. Haematology
  • Not labelled yet21st Annual Sickle Cell & Thalassaemia Conference, 7-10 October 2026, London.British journal of haematology
  • ReviewAn evaluation of mitapivat for the treatment of non-transfusion-dependent alpha- and beta-thalassemia.Therapeutic delivery
  • Not labelled yetα-thalassaemia: an overlooked disease entering a new era.The Lancet. Haematology
  • Not labelled yetFrom pain to purpose: my thalassaemia journey.The Lancet. Haematology
  • Not labelled yetThalassaemia revisited: whose progress?The Lancet. Haematology
  • Not labelled yetSOME HEREDITARY DISEASES PREVALENT IN THE REPUBLIC OF AZERBAIJAN.Georgian medical news
  • Not labelled yetCost-effectiveness and budget impact of Luspatercept in Thai adults with transfusion-dependent beta-thalassaemia: a multi-state Markov model based on national claims data.Journal of pharmaceutical policy and practice
  • Not labelled yetβ-thalassemia as a progressive disease: age-related morbidity in the de-LIGHT study.Haematologica
  • Not labelled yetFunctional alterations of neutrophils from β-thalassemia patients exposed to Pythium insidiosum: An ex vivo study.PloS one
  • Not labelled yetReactivation of the embryonic ζ-globin gene ameliorates severe forms of α-thalassemia.Nature genetics
  • Not labelled yetFPN1-8C>G Polymorphism as a potential genetic modifier of iron overload in transfusion-dependent β-Thalassemia major patients receiving HbF augmentation therapy.Pakistan journal of medical sciences
  • ReviewCaries Experience in Children and Adolescents With Thalassemia: A Systematic Review and Meta-Analysis.Caries research
  • Not labelled yetFlipping the fetal switch across β-hemoglobinopathies.Cell stem cell
  • Not labelled yetAnalysis of various electrocardiographic and echocardiographic parameters in beta thalassemia patients with iron overload.Annals of pediatric cardiology
  • Not labelled yetSubclinical cardiac dysfunction in transfusion-dependent beta-thalassemia children, an experience from central India: A comparative cross-sectional study.Annals of pediatric cardiology
  • Not labelled yetPrecision base-editing of the cryptic 3' acceptor site to correct the RNA splicing defect of β654-thalassemia.Molecular biomedicine
  • Not labelled yetCost-Effectiveness of Peripheral Neuropathy Screening in Patients With Thalassemia: A Hybrid Decision-Markov Model.Value in health regional issues
  • Case reportCase 354.Radiology
  • Case reportChallenges in Glycemic Monitoring: Undetectable HbA1c Level in an Asymptomatic Patient With Hemoglobin E and Beta-Thalassemia Minor: A Case Report.Journal of the ASEAN Federation of Endocrine Societies
  • Not labelled yet[Application of Next-Generation Sequencing Technology in Genetic Screening for Thalassemia in Zhangzhou Area].Zhongguo shi yan xue ye xue za zhi
  • Not labelled yetSuccessful Management of Severe Hepatic Acute Graft-Versus-Host Disease After Allogeneic Hematopoietic Stem Cell Transplantation in a Child With β-Thalassemia Major: Clinical Lessons From Early Therapeutic Escalation.Clinical case reports
  • Not labelled yetMultisystem Complications in Non-Transfusion-Dependent β-Thalassemia Intermedia: A Case Highlighting the Need for Early Intervention.Clinical case reports
  • Not labelled yetDevelopment of Gap-Recombinase Polymerase Amplification Combined with CRISPR-Cas12a (Gap-RPA/CRISPR-Cas12a) for Rapid Screening of α0-Thalassemia Southeast Asian (--SEA) Deletion and Thai (--THAI) Deletion.Biology
  • Not labelled yetEffect of HFE Gene H63D and S65C Mutations on the Severity of Secondary Iron Overload in Children With β-Thalassemia Major.Cureus
  • Not labelled yetMutations in Distal Cis-Regulatory Elements in the Beta Globin (HBB) Gene Promoter of Filipinos Influences Transcriptional Activity.Genes
  • ReviewClinical Implications of Sickle Cell Thalassemia on Pregnancy Outcomes: A Systematic Review.Diagnostics (Basel, Switzerland)
  • Not labelled yetAge-Related Patterns of Organ-Specific Iron Distribution in Non-Transfusion-Dependent Thalassemia: A Multicenter MRI Study.Journal of clinical medicine
  • Not labelled yetPaediatric Splenectomy at the National Centre for Paediatric Surgery, Sudan: A Five-Year Cross-Sectional Retrospective Study.African journal of paediatric surgery : AJPS
  • Not labelled yetLeg Ulcers in Thalassaemia: A Comparative Retrospective Review of Transfusion-Dependent and Non-Transfusion-Dependent Patients.International wound journal
  • Case reportAcute hemolytic transfusion reaction mediated by anti-Jkb antibody in a pediatric patient with β-thalassemia major: a case report illustrating an anamnestic alloimmune response.Frontiers in immunology
  • Not labelled yetAlpha-thalassaemia: from regional burden to global priority.The Lancet regional health. Southeast Asia
  • Not labelled yetClinical, Hematological, and Nutritional Profiling of Thalassemia Patients: Insights From a Cross-Sectional Study.Anemia
  • ReviewHemoglobinopathies and Thalassemia in Northeast India: A Scoping Review of Disease Burden, Mutation Spectrum, and Gaps in Molecular Genetic Evidence.Cureus
  • Not labelled yetDifferentiating β-Thalassaemia From Iron Deficiency: Performance and Cut-Off Dependency of More Than 40 Red Cell Discrimination Indices in a Large German Cohort.International journal of laboratory hematology
  • Not labelled yetLongitudinal changes in pancreatic iron burden in non-transfusion-dependent thalassemia: A multicenter MRI study.Blood cells, molecules & diseases
  • ReviewCRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.Hemoglobin
  • Not labelled yetGenotypic distribution and molecular spectrum of rare and novel thalassemia variants in Ganzhou, southern China.Frontiers in molecular biosciences
  • ReviewEndocrine dysfunction in transfusion-dependent and non-transfusion-dependent beta-thalassemia: a systematic review and meta-analysis.Hormone molecular biology and clinical investigation
  • Not labelled yetPancreatic iron overload as a marker of endocrine complications in transfusion-dependent thalassaemia: A multicentre study.British journal of haematology
  • Not labelled yetFactors Contributing to Improved Bone Mineral Density in Patients With Transfusion-Dependent Thalassemia.The Kaohsiung journal of medical sciences
  • Not labelled yetNanoplate Digital PCR for Identification of α0-Thalassemia (SEA Deletion): Carrier Screening and Possible Application to Prenatal Diagnosis.International journal of molecular sciences
  • Not labelled yetGenotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.Hemoglobin
  • Not labelled yetRight ventricular-pulmonary arterial coupling in transfusion-dependent thalassemia: a cross-sectional cardiac MRI study.European radiology
  • Not labelled yetDevelopment and Internal Validation of a Machine Learning-Based Model for Thalassemia Identification Using Complete Blood Count Parameters.Diagnostics (Basel, Switzerland)
  • Not labelled yetCharacterisation of clinical, hematological and molecular variability in individuals with sickle β-thalassemia.Blood cells, molecules & diseases
  • Not labelled yetDiagnostic Challenges of Hemoglobin (Hb) Hekinan with deletional α0-thalassemia and β0-thalassemia During Prenatal Screening for Fetal Hb E/β-Thalassemia Risk.Mediterranean journal of hematology and infectious diseases
  • Not labelled yetMandibular Osseous Changes in Children and Adolescents With Beta Thalassemia Major: A Panoramic Radiomorphometric Study.Cureus
  • Not labelled yetMapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.Hemoglobin
  • Not labelled yetMitapivat for transfusion-dependent α-thalassaemia and β-thalassaemia.Lancet (London, England)
  • Randomised trialEfficacy and safety of mitapivat in adults with transfusion-dependent α-thalassaemia or β-thalassaemia (ENERGIZE-T): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial.Lancet (London, England)
  • Case reportBK virus-associated haemorrhagic cystitis following allogeneic haematopoietic stem cell transplantation in a paediatric patient with β-thalassaemia major: A case report.Indian journal of medical microbiology
  • Not labelled yetOcular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.Hemoglobin
  • Not labelled yetMolecular profiling of thalassemia in Southeastern Romania.Journal of hematopathology
  • Not labelled yetHematological Profile in Co-Inherited β -Thalassemia Trait with IVS 1-5 (G→C) Mutation and α+-Thalassemia.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
  • Not labelled yetA machine-learning capillary electrophoresis-based pattern to identify suspected sickle cell trait and α-thalassemia co-inheritance.Advances in laboratory medicine
  • Not labelled yetCoagulation Defects in Hemoglobin E β Thalassemia Patients: A Study from a Thalassemia Care Centre (TCU) in Kolkata, India.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
  • Not labelled yetSafety and Effectiveness of Thalidomide in Transfusion-Dependent and Non-Transfusion-Dependent Thalassaemia Children in Eastern India.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
  • Not labelled yetUnderstanding the Endocrine Consequences of Transfusion-Dependent Thalassemia: A Detailed Exploration of Key Influences.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
  • Not labelled yetInteraction of an α-globin Gene Triplication with Other Forms of Thalassemia or Hemoglobinopathy in Northern Thailand.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
  • Not labelled yetDiagnostic Pitfall in β-Thalassemia Trait Screening: A Case of Hb Showa-Yakushiji (HBB:c.332T > C) Coinherited with Gilbert Syndrome.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
  • Not labelled yetSeroprevalence of Toxoplasma gondii among Children with Beta-thalassemia Major and its Effect on Selected Immune Parameters.Turkiye parazitolojii dergisi
  • Not labelled yetThe worth of diffusion-weighted imaging for quantifying liver iron concentration in transfusion-dependent thalassemia patients.Acta radiologica (Stockholm, Sweden : 1987)
  • Not labelled yetMolecular genetics analysis of genes BCL11A, HBS1L-MYB, and HBG2 variants association in thalassemic children.Personalized medicine
  • Not labelled yetControlling Hemoglobin F Expression in Sickle Cell Disease and β-thalassemia.Transfusion medicine reviews
  • Not labelled yetBisphosphonate therapy for thalassemia-related bone disorders in children and young adults: a systematic review.Annals of pediatric endocrinology & metabolism
  • Not labelled yetClinical base editing for β-hemoglobinopathies across different genetic backgrounds.Cell stem cell
  • Not labelled yetThalassemia in Iraq: Time to Reform Policy.Rwanda journal of medicine and health sciences
  • Not labelled yetContemporary Management of Thalassemia: A Perspective on Current Standards and the Emergence of FDA-Approved Oral Therapy.Health science reports
  • Not labelled yetPreclinical evaluation of entecavir as a fetal hemoglobin inducer using in vitro, in vivo, network pharmacology, and molecular docking approaches.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
  • Not labelled yetIron chelation therapy and splenomegaly severity in transfusion dependent beta thalassemia major: assessment of ferritin patterns and clinical outcomes.Naunyn-Schmiedeberg's archives of pharmacology
  • Not labelled yetBurden of sickle cell disease among pregnant women in central India.The Indian journal of medical research
  • Not labelled yetHematologic Indices of Hemoglobin D Co-Inheritance with α and β Thalassemia: A Comparative Study of 202 Patients.Hemoglobin
  • Not labelled yetILF3 regulates erythroid differentiation: A single-cell transcriptomic analysis and cellular experiment.PloS one
  • ReviewHemoglobinopathies and Cellular Therapy: What Pediatricians Need to Know About Indications and Counseling.Pediatric annals
  • Case reportLongstanding Microcytosis with a Thalassaemia-Like Phenotype and Inconclusive Molecular Testing: A Case Report.Journal of blood medicine
  • Not labelled yetEfficacy and safety of thalidomide (1 vs 2 mg/kg/d) in transfusion-dependent thalassemia: A Non-Inferiority Trial.Blood advances
  • Not labelled yetHaploidentical haematopoietic stem cell transplantation for thalassaemia major: A phase IV, open-label, single-centre trial.British journal of haematology
  • Not labelled yetAnalysis of microRNA-451 gene expression and its association with liver function tests in β-thalassemia major.Folia medica
  • ReviewChanging the treatment paradigm in beta thalassemia.Folia medica
  • Not labelled yetCharacterization of oral microbiome alterations in thalassemia patients using 16S rRNA gene sequencing.Frontiers in microbiology
  • Not labelled yetPreanalytical stability of hemoglobin H inclusion body detection using rapid brilliant cresyl blue staining: a genotype-stratified stability study in EDTA blood stored at 4 °C.Laboratory medicine
  • ReviewNon-transfusion-dependent β-thalassemia: A disease of clinical paradoxes.Blood reviews
  • Not labelled yetMedication Adherence, Clinical Outcomes, and Health-Related Quality of Life Among Pediatric Patients with β-Thalassemia Major Receiving Iron Chelation Therapy: A Multicenter Study from Punjab, Pakistan.Patient preference and adherence
  • Not labelled yetAssociation of age and serum ferritin with audiometric hearing loss in transfusion-dependent β thalassemia.American journal of otolaryngology
  • Not labelled yetOrthodontic and Craniofacial Skeletal Alterations in Individuals With Thalassemia: A Scoping Review.Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry
  • Not labelled yetBrazilin reduces toxic iron species and oxidative damage in iron-loaded β-thalassemic mice.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
  • Not labelled yetEligibility of blood donors with thalassaemia trait, sickle cell trait or glucose-6-phosphate-dehydrogenase deficiency in Italy: Results of a national survey and practical guidance.Vox sanguinis
  • Not labelled yetBeta-Globin (HBB) Mutations and Catalase Gene Polymorphisms in Beta-Thalassemia Major Patients in Al-Diwaniyah, Iraq.Genes