Disease: Sickle cell anemia
- A Novel Mechanistic Model for Future Research in the Elements of the ERAS Program in Patients With Sickle Cell Disease
- A Rare Case of Brodie's Abscess in the Tibial Diaphysis Masquerading as a Vaso-occlusive Sickle Crisis
- A Saudi Woman with Ceftriaxone Induced Fixed Drug Eruption
- Acute care utilization among individuals with sickle cell disease and related cardiopulmonary and renal complications
- Acute Weakness in a Toddler with Sickle Cell Disease
- Aerobic physical capacity and health-related quality of life in children with sickle cell disease
- Age-related Morphofunctional Changes in Sickle Cell Mice Bone Marrow Mesenchymal Stromal Cells
- Ago Sankofa: an overview of the progression of sickle cell disease in Brazil in the past two decades
- An assessment of the psychometric properties of the Coping Strategies Questionnaire - Sickle Cell Disease (CSQ-SCD) among adults in the United States
- Anogeissus leiocarpus (DC.) Guill. & Perr. (Combretaceae): A review of the traditional uses, phytochemistry and pharmacology of African birch
- Assessing the Quality of Care for Children With Sickle Cell Anemia: We Are Still Failing
- Assessment of hypoxemia among young adults with sickle cell anaemia in steady state in southwestern Nigeria: a crosssectional study
- Beyond adenosine triphosphate: unveiling the pleiotropic effects of pyruvate kinase activation in sickle cell anemia
- 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
- Blood count changes in malaria patients according to blood groups (ABO/Rh) and sickle cell trait
- Bone Health Impairment in Patients with Hemoglobinopathies: From Biological Bases to New Possible Therapeutic Strategies
- Brain network hypersensitivity underlies pain crises in sickle cell disease
- Cas9 RNP Physiochemical Analysis for Enhanced CRISPR-AuNP Assembly and Function
- Circulation chez des patients drépanocytaires : en finir avec les bouchons
- Comment on "The association of sickle cell disorder with adverse outcomes in COVID-19 patients: A meta-analysis"
- Compare the Efficacy and Safety of Deferoxamine, Deferasirox, and Deferiprone in Patients With Sickle Cell Disease or Transfusion-Dependent Anemia: A Network Meta-Analysis of Randomized Control Trials
- Consanguineous marriages, premarital screening, and genetic testing: a survey among Saudi university students
- 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
- Decreased risk of underdosing with continuous infusion versus intermittent administration of cefotaxime in patients with sickle cell disease and acute chest syndrome
- Dental Caries in Children with Sickle Cell Disease and Its Association with the Use of Hydroxyurea and Penicillin Prophylaxis in Dar Es Salaam
- Dental caries in the permanent dentition and health-related quality of life among children and adolescents with sickle cell disease
- Dental Management of a Child With Sickle Cell Anemia: A Case Report
- Description of a national, multi-center registry of patients with sickle cell disease and SARS-CoV-2 infection: Data from the Pediatric COVID-19 United States Registry
- DISPLACE Study Shows Poor Quality of Transcranial Doppler Ultrasound for Stroke Risk Screening in Sickle Cell Anemia
- Distribution of Silent Cerebral Infarcts in Adults With Sickle Cell Disease
- Early diagnosis of sickle cell retinopathy by using ocular coherence tomography in pediatric population (7-18 years) in central India
- 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
- Experiences and strategies of people with sickle cell disease in the Federal District: the biographical rupture
- Exploring Factors Associated with Quality of Life in Caregivers of Children and Adolescents with Sickle Cell Disease and HIV: A Comparative Analysis
- Factors associated with adverse outcome among children with sickle cell disease admitted to the pediatric intensive care unit: an observational cohort
- First Gene Therapies Approved for Sickle Cell Disease
- 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
- Gut Microbiota: Potential Therapeutic Target for Sickle Cell Disease Pain and Complications
- 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
- Hemolysis impairs sickle cell erythropoiesis
- High-mobility group box 1 increases platelet surface P2Y12 and platelet activation in sickle cell disease
- How healthy is the health budget of <em>Amrit Kaal</em>: 2023-24?
- Impact of Hydroxyurea on Clinical and Biological Parameters of Sickle Cell Anemia in Children in Abidjan
- Impact of SARS-CoV-2 infection on pain crisis and acute chest syndrome in patients with sickle cell anemia: A retrospective multi-cohort study based on US national data from 2020 to 2022
- Influence of hydroxyurea on tubular phosphate handling in sickle cell nephropathy
- Innovators want pills to treat sickle cell disease. Can they match gene therapy?
- Laparoscopic Cholecystectomy in Jos: Prospects and Perspectives
- Left ventricular global longitudinal strain and acute myocardial injury in patients with sickle cell disease admitted to the intensive care unit for vaso-occlusive crisis
- Letter to the editor: TRADOC policy does not list sickle cell trait as a risk factor for cold injury
- 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
- Maximizing longevity: erythropoietin's impact on sickle cell anaemia survival rates
- Measuring haemoglobin concentration to define anaemia: WHO guidelines
- Migrant Pathology Screening in the Pediatric Population: A Five-Year Retrospective Study From a Level II Hospital
- Multi-center study on mortality in children, and adults with sickle cell anemia-risk factors and causes of death
- Multiparametric Cardiac Magnetic Resonance Assessment in Sickle Beta Thalassemia
- National Quality Indicators in Pediatric Sickle Cell Anemia
- Newborn screening in Colombia: The experience of a private program in Bogotá
- On the feasibility of malaria hypothesis
- Optimization of single-needle red cell exchange in patients with sickle cell disease
- Partial Splenic Embolization in Paediatric Sickle Cell Disease Patients with Hypersplenism
- Pharmacogenomics of Drugs Used in beta-Thalassemia and Sickle-Cell Disease: From Basic Research to Clinical Applications
- Population characterization of mutations for sickle cell anemia and its treatment: One step towards personalized medicine for the disease
- Prevalence and predictors of iron deficiency anaemia among children with sickle cell disease in Dodoma, Tanzania: a cross-sectional study
- Prevalence of Duffy null and its impact on hydroxyurea in young children with sickle cell disease in the United States
- Recruitment and Retention of Hematopoietic Cell Transplantation and Cellular Therapy Physicians: A Report from the ASTCT Talent Acquisition Task Force
- Recurrent musculoskeletal pain and hemoglobin SC disease
- Risk factors for acute chest syndrome among children with sickle cell anemia hospitalized for vaso-occlusive crises
- SARS-CoV-2 with Influenza B Coinfection in a Patient with Sickle Cell HbSC Presenting with Painful Crisis: A Case Report
- Serum iron Profile of Patients with Sickle Cell Disease and its Association with Socio-demographic Characteristics and Duration of Diagnosis
- Sickle cell anemia: hepatic macrophages to the rescue
- Sickle Cell Anomaly Meets Leukemic Challenge: A Case Report
- Sickle cell disease and increased adverse maternal and perinatal outcomes in different genotypes
- 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 Health Awareness, Perspectives, and Experiences (SHAPE) survey: Perspectives of adolescent and adult patients, caregivers, and healthcare professionals on the burden of sickle cell disease
- Sickle cell trait in Sao Tome e Principe: a population-based prevalence study in women of reproductive age
- Silent Cerebral Infarcts in Adults With Sickle Cell Disease: Expanding Beyond Childhood Borders
- Social determinants of health and treatment center affiliation: analysis from the sickle cell disease implementation consortium registry
- Spontaneous epidural haematoma in a paediatric patient with sickle cell disease
- Substance use disorder of equimolar oxygen-nitrous oxide mixture in French sickle-cell patients: results of the PHEDRE study
- The Associations Between Opioid Use Disorder and Healthcare-Related Outcomes in Vaso-occlusive Crisis
- The RoxyScan is a novel measurement of red blood cell deformability under oxidative and shear stress
- The transition of adolescents with sickle cell disease: an interdisciplinary exchange
- 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
- TSH Receptor Reduces Hemoglobin S Polymerization and Increases Deformability and Adhesion of Sickle Erythrocytes
- Validating evidence for the knowledge, management and involvement of dentists in a dental approach to sickle-cell disease
- Vaso-Occlusive Crises in Sickle Cell Trait Patients With Blood Loss Anemia: A Report of Two Cases
- Yoga Module Development and Validation for Sickle Cell Disease