Disease: Hemoglobinopathy
- 5-HT3 antagonist, tropisetron, ameliorates age-related renal injury induced by D-galactose in male mice: Up-regulation of sirtuin 1
- A New α1-Globin Variant, Hb Ormylia [<em>HBA1</em>:c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece
- A Novel Mechanistic Model for Future Research in the Elements of the ERAS Program in Patients With Sickle Cell Disease
- A novel α<sup>0</sup>-thalassemia deletion in a Brazilian child with Hb H disease: --<sup>Mococa</sup>
- A Rare Presentation of Extramedullary Hematopoiesis as an Adrenal Mass: A Case Report
- A scoping review exploring cure definitions and language for inherited hemoglobinopathies
- A singleton pregnancy with placental chorioangioma and hydrops fetalis complicated with mirror syndrome and ritodrine-induced side effects: a case report
- Abnormal hemoglobin anti-Lepore Hong Kong compound with β<sup>0</sup>-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia
- Acute care utilization among individuals with sickle cell disease and related cardiopulmonary and renal complications
- Acute Graft versus Host Disease in Beta Thalassemia Patients Following Allogeneic Haematopoietic Stem Cell Transplantation
- Acute Liver Failure With Liver Enzymes >5,000 in Sickle Cell Disease
- Addressing Thalassaemia Management from Patients' Perspectives: An International Collaborative Assessment
- Advance of research on the role of BCL11A in the occurrence and treatment of β-Thalassemia
- Age-related Morphofunctional Changes in Sickle Cell Mice Bone Marrow Mesenchymal Stromal Cells
- An assessment of the psychometric properties of the Coping Strategies Questionnaire - Sickle Cell Disease (CSQ-SCD) among adults in the United States
- Analysis of Plasma Metabolic Profile in Children with Transfusion-Dependent Thalassemia
- Angioid Streaks Remain a Challenge in Diagnosis, Management, and Treatment
- Appropriate whole genome amplification and pathogenic loci detection can improve the accuracy of preimplantation genetic diagnosis for deletional α-thalassemia
- Assessment of hypoxemia among young adults with sickle cell anaemia in steady state in southwestern Nigeria: a crosssectional study
- Biased agonism of protease-activated receptor-1 regulates thrombo-inflammation in murine sickle cell disease
- Birth Prevalence of Sickle Cell Disease and County-Level Social Vulnerability - Sickle Cell Data Collection Program, 11 States, 2016-2020
- Brain network hypersensitivity underlies pain crises in sickle cell disease
- Butyric acid and prospects for creation of new medicines based on its derivatives: a literature review
- Case Report: Obstetric and COVID-19-Related Morbidity and Mortality in Three Patients with Sickle Hemoglobinopathy
- Cases Analysis of Hemoglobin H Disease Caused by <em>HBA2:c.2T>C</em> and <em>HBA2:c.2delT</em> Mutations
- Changing epidemiology of parvovirus B19 in the Netherlands since 1990, including its re-emergence after the COVID-19 pandemic
- Circulation chez des patients drépanocytaires : en finir avec les bouchons
- Comparing three cardiothoracic ratio measurement techniques and creating multivariable scoring system to predict Bart's hydrops fetalis at 17-22 weeks' gestation
- Current obstetric outcomes in Jamaican women with sickle hemoglobinopathy - a balance of risks for aspirin?
- Cystatin C Outperforms Creatinine in Predicting Cefepime Clearance in Pediatric Stem Cell Transplant Recipients
- Decreased risk of underdosing with continuous infusion versus intermittent administration of cefotaxime in patients with sickle cell disease and acute chest syndrome
- Determining factors of pulse oximetry accuracy: A literature review
- Droplet digital polymerase chain reaction-based quantitation of therapeutic lentiviral vector copies in transduced hematopoietic stem cells
- Early Screening Of Sickle Cell Disease: Knowledge And Behaviors Of Pregnant Women And Health Workers In Burkina Faso
- Early-onset indicators of a hypercoagulable state and clinical complications in a cohort of children with sickle cell trait
- Editorial: Recent advances in pediatric red blood cells disorders
- Effect of nutritional supplementation on bone mineral density in children with sickle cell disease: protocol for an open-label, randomised controlled clinical trial
- Endari treatment ameliorates sickle cell-related disruption in intestinal barrier functions and is associated with prolonged survival in sickle cell mice
- Endurance training and hydroxyurea have synergistic effects on muscle function and energetics in sickle cell disease mice
- Evaluation of Intestinal Microbiota in Children With Sickle Cell Disease: Erratum
- Fetal anemia causes placental and maternal cellular damage: a lesson from fetal hemoglobin Bart's disease
- Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel
- Genetic Modifiers of Sickle Cell Anemia Phenotype in a Cohort of Angolan Children
- Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis
- Genome-Wide Analysis of Exertional Rhabdomyolysis in Sickle Cell Trait Positive African Americans
- Glad tidings and joy for children with SCA
- Good engraftment after reduced intensity targeted busulfan-based conditioning and matched related donor hematopoietic cell transplantation in hemoglobinopathies
- Green Formulation of Spironolactone Loaded Chitosan-Coated Nano Lipid Carrier for Treatment of Acne Vulgaris: A Randomized Double-Blind Clinical Trial
- Growth and endocrinopathies among children with β-Thalassemia major treated at Dubai Thalassemia centre
- Hb H disease associated with compound heterozygosity for --<sup>SEA</sup> deletion and a novel alpha globin chain variant (<em>HBA2</em>:c.175C>A) on the distal histidine in a Chinese family
- Health education to promote knowledge about sickle cell disease and newborn screening in pregnant women: a community-based pilot study using the healthy beginning initiative
- Idiopathic Thrombocytosis in Alpha Thalassemia Trait Patient
- Impact of alpha-Globin Gene Expression and alpha-Globin Modifiers on the Phenotype of beta-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management
- Improving access to gene therapy for rare diseases
- Iowa Newborn Screening Program Experience with Hemoglobinopathy Screening over the Last Two Decades and Its Increasing Global Relevance
- Is There any Relationship Between the Repeated Complications of Sickle Cell Disease and the Potential Development of Acute Leukemia?
- Letter to the Editor: Management of Pregnancies Alloimmunized with Non-Rh and Non-K Alloantibodies
- Lower Arginine Bioavailability, Increased FeNO Levels, and Airway Resistance on Impulse Oscillometry Are Characteristics of Asthma in Children and Young Adults with Sickle Cell Disease
- Machine learning evaluation for identification of M-proteins in human serum
- Management of diabetes mellitus patients with sickle cell anemia: Challenges and therapeutic approaches
- miR-214 aggravates oxidative stress in thalassemic erythroid cells by targeting ATF4
- MIR96 Has Good Potential to Differentiate Human Bone Marrow-Derived Mesenchymal Stem Cells into Photoreceptor-Like Cells
- Molecular epidemiology and hematological profiles of hemoglobin variants in southern Thailand
- Multi-center study on mortality in children, and adults with sickle cell anemia-risk factors and causes of death
- Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation (<em>HBB</em>:c.336dup)
- Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage
- Opioid Use Among Children and Adults With Sickle Cell Disease in North Carolina Medicaid Enrollees in the Era of Opioid Harm Reduction
- Perinatal Results and Long-Term Follow-Up of Fetal Cardiac Tumors: A 30-Year Historical Cohort Study
- Peripheral Neuropathy in Patients with Hepatitis C Infection-Reversibility after HCV Eradication: A Single Center Study
- Pharmacogenomics of Drugs Used in β-Thalassemia and Sickle-Cell Disease: From Basic Research to Clinical Applications
- Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life
- Population characterization of mutations for sickle cell anemia and its treatment: One step towards personalized medicine for the disease
- Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq
- Prevalence and predictors of iron deficiency anaemia among children with sickle cell disease in Dodoma, Tanzania: a cross-sectional study
- Prevalence of fetomaternal Rhesus incompatibility at the tertiary care hospital: a cross-sectional study
- Progress in the Genetic Detection of Thalassemia Based on Third-Generation Gene Sequencing --Review
- Proportion of Hypogonadism in Transfusion-Dependent Thalassemia Patients and Its Contributing Factors
- Recurrent musculoskeletal pain and hemoglobin SC disease
- Rehabilitation Strategies for Wrist Pain in a Patient With Thalassemia Major and Distal Ulnar Hypoplasia: A Case Report
- SARS-CoV-2 with Influenza B Coinfection in a Patient with Sickle Cell HbSC Presenting with Painful Crisis: A Case Report
- Secondary amenorrhea in a β-thalassemia major patient treated with thalidomide
- Serum iron Profile of Patients with Sickle Cell Disease and its Association with Socio-demographic Characteristics and Duration of Diagnosis
- Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D <em>HBA1</em>: C.119_121delCCA Mutation and <em>HBA2</em>: C.*94A > G Mutation
- Sickle cell disease in the kidney transplant
- Sickle cell disease in the Zanzibar Archipelago, the Republic of Tanzania
- Sickle Cell Disease Phenotypes and Obstructive Sleep Apnea; Are They Related?
- Significant Inverse Correlation of Serum Levels of Osteoprotegerin (OPG) and Transferrin Saturation in Thalassemia Dependent Transfusion (TDT) Patients
- Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with beta-thalassemia
- Spontaneous epidural haematoma in a paediatric patient with sickle cell disease
- 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
- Syracuse Hemoglobinopathy Presenting With Tophaceous Gout: A Case Report
- Systematic Review and Meta-Analysis of Health-Related Quality of Life in Patients with β-Thalassemia that Underwent Hematopoietic Stem Cell Transplantation
- The acute pain crisis in sickle cell disease: What can be done to improve outcomes?
- Therapeutic effect of ferrous sulfate in diabetic patients with iron deficiency anaemia: a randomised controlled trial
- Thrombin activatable fibrinolysis inhibitor plasma levels and TAFI Thr325Ile genetic polymorphism in a cohort of Egyptian sickle cell disease patients and impact on disease severity
- Transition in sickle cell disease - recommendations of the transition initiative sickle cell disease
- Translational Research and Health Equity: Gene Therapies for Sickle Cell Disease as a Case Study
- Unraveling DEHP influence on hemoglobin S polymerization in sickle cell disease: Ex vivo, in vitro and in silico analysis
- Validating evidence for the knowledge, management and involvement of dentists in a dental approach to sickle-cell disease