Disease: Congenital hemolytic anemia
- 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
- 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 Weakness in a Toddler with 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
- Alexis Thompson: advancing care for sickle cell disease
- 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
- 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
- Birth Prevalence of Sickle Cell Disease and County-Level Social Vulnerability - Sickle Cell Data Collection Program, 11 States, 2016-2020
- Blood count changes in malaria patients according to blood groups (ABO/Rh) and sickle cell trait
- Brain network hypersensitivity underlies pain crises in sickle cell disease
- Cases Analysis of Hemoglobin H Disease Caused by <em>HBA2:c.2T>C</em> and <em>HBA2:c.2delT</em> Mutations
- Circulation chez des patients drépanocytaires : en finir avec les bouchons
- Cognitive impairment and hippocampal neuronal damage in β-thalassaemia mice
- Comparing three cardiothoracic ratio measurement techniques and creating multivariable scoring system to predict Bart's hydrops fetalis at 17-22 weeks' gestation
- Cost analysis for initiating an integrated package of essential non-communicable disease interventions (PEN-Plus) in Kondoa District Hospital, Tanzania: a time-driven activity-based costing (TDABC) study protocol
- Could the 14q23.2 microdeletion or AKAP5 haploinsufficiency be a potential cause of intellectual disability?
- Decreased risk of underdosing with continuous infusion versus intermittent administration of cefotaxime in patients with sickle cell disease and acute chest syndrome
- Distribution of Silent Cerebral Infarcts in Adults With Sickle Cell Disease
- Early-onset indicators of a hypercoagulable state and clinical complications in a cohort of children with sickle cell trait
- 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
- Et barn med langvarig anemi
- 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
- Field evaluation of a novel semi-quantitative point-of-care diagnostic for G6PD deficiency in Indonesia
- Generation and analysis of TPI deficiency zebrafish model
- Genetic Analysis of Two Novel GPI Variants Disrupting H Bonds and Localization Characteristics of 55 Gene Variants Associated with Glucose-6-phosphate Isomerase Deficiency
- 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
- Gestational alloimmune liver disease with alpha thalassaemia in a neonate
- Glad tidings and joy for children with SCA
- Glucose phosphate isomerase deficiency demasked by whole-genome sequencing: a case report
- 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
- Hematopoietic Stem Cell Transplantation in Sickle Cell Disease: A Multidimentional Review
- Identification of a novel splice variant in SEC23B gene in a patient with concomitant presence of congenital dyserythropoietic anemia II and Gilbert's syndrome
- Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis
- Idiopathic Thrombocytosis in Alpha Thalassemia Trait Patient
- Impact of α-Globin Gene Expression and α-Globin Modifiers on the Phenotype of β-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management
- In brief: Casgevy for beta thalassemia
- 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
- Management of diabetes mellitus patients with sickle cell anemia: Challenges and therapeutic approaches
- Managing gastrointestinal challenges: Diarrhea in sickle cell anemia
- miR-214 aggravates oxidative stress in thalassemic erythroid cells by targeting ATF4
- Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing
- Molecular Characterization of α- and β-Thalassemia Among Children Less Than 18 Years Old in Guizhou, China
- 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)
- Newborn screening in Colombia: The experience of a private program in Bogotá
- Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage
- Novel mutation in KIF23 causing congenital dyserythropoietic anemia type III in patients who underwent allogeneic hematopoietic stem cell transplantation
- Opioid Use Among Children and Adults With Sickle Cell Disease in North Carolina Medicaid Enrollees in the Era of Opioid Harm Reduction
- Optimization of single-needle red cell exchange in patients with sickle cell disease
- Pharmacogenomics of Drugs Used in β-Thalassemia and Sickle-Cell Disease: From Basic Research to Clinical Applications
- PKLR mutations in pyruvate kinase deficient Polish patients: Functional characteristics of c.101-1G > A and c.1058delAAG variants
- 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
- Progress in the Genetic Detection of Thalassemia Based on Third-Generation Gene Sequencing --Review
- Prolonged Fever in a 3-Year-Old With Sickle Cell Disease
- Proportion of Hypogonadism in Transfusion-Dependent Thalassemia Patients and Its Contributing Factors
- Quantifying the effect of glucose 6-phosphate dehydrogenase deficiency on glycated hemoglobin values in children and adolescents with type 1 diabetes
- Recurrent musculoskeletal pain and hemoglobin SC disease
- Riociguat in patients with sickle cell disease and hypertension or proteinuria (STERIO-SCD): a randomised, double-blind, placebo controlled, phase 1-2 trial
- Riociguat shows remarkable safety but underwhelming activity in patients with sickle cell disease
- 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 India: current status and progress
- 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?
- Sickle Cell Disease Related Vasculopathies and Early Evaluation in a Pediatric Population
- Sickle cell trait in São Tomé e Príncipe: a population-based prevalence study in women of reproductive age
- Sickle cell: NICE approves voxelotor after initially rejecting it over uncertain evidence
- Significant Inverse Correlation of Serum Levels of Osteoprotegerin (OPG) and Transferrin Saturation in Thalassemia Dependent Transfusion (TDT) Patients
- Silent Cerebral Infarcts in Adults With Sickle Cell Disease: Expanding Beyond Childhood Borders
- Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with β-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
- Syk inhibition suppresses NLRP3 inflammasome activation in platelets from sickle cell mice leading to decreased platelet secretion, aggregation, spreading, and in vitro thrombus formation
- The acute pain crisis in sickle cell disease: What can be done to improve outcomes?
- The effect of glucose-6-phosphate dehydrogenase deficiency on allogeneic hematopoietic stem cell transplantation in patients with hematological disorders
- 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
- Using the daily rate of rise in hemoglobin S to manage RBC depletion/exchange treatment in sickle cell disease
- Validating evidence for the knowledge, management and involvement of dentists in a dental approach to sickle-cell disease
- β-Thalassemia gene editing therapy: Advancements and difficulties