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Subject Areas on Research
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"It Is Not Easy": Cultural Influences of Sickle Cell Disease Management in Rural, Eastern Sierra Leone.
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"Pain is Subjective": A Mixed-Methods Study of Provider Attitudes and Practices Regarding Pain Management in Sickle Cell Disease Across Three Countries.
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9p- in a girl with acute lymphocytic leukemia and sickle cell disease.
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A Biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease
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A Prospective Emergency Department Quality Improvement Project to Improve the Treatment of Vaso-Occlusive Crisis in Sickle Cell Disease: Lessons Learned.
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A Survey-Based Needs Assessment of Barriers to Optimal Sickle Cell Disease Care in the Emergency Department.
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A benign sickle-cell disease in a Saudi subject with beta zero-thalassemia and glucose-6-phosphate dehydrogenase deficiency.
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A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.
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A case for community health programs for sickle cell anemia in low- to middle-income countries: An integrative review.
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A case series describing causes of death in pregnant women with sickle cell disease in a low-resource setting.
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A common functional PIEZO1 deletion allele associates with red blood cell density in sickle cell disease patients.
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A comparison of analgesic management for emergency department patients with sickle cell disease and renal colic.
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A double-blind, randomized, multicenter phase 2 study of prasugrel versus placebo in adult patients with sickle cell disease.
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A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
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A multi-institutional comparison of younger and older adults with sickle cell disease.
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A phase I/II study of polymerized bovine hemoglobin in adult patients with sickle cell disease not in crisis at the time of study.
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A pilot study of hydroxyurea to prevent chronic organ damage in young children with sickle cell anemia.
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A prospective study of the relationship over time of behavior problems, intellectual functioning, and family functioning in children with sickle cell disease: a report from the Cooperative Study of Sickle Cell Disease.
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A qualitative analysis of best self-management practices: sickle cell disease.
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A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis.
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A randomized controlled trial comparing two vaso-occlusive episode (VOE) protocols in sickle cell disease (SCD).
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A reanalysis of pain crises data from the pivotal l-glutamine in sickle cell disease trial.
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A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease
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A study of oral pain experience in sickle cell patients.
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A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease.
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A telephonic mindfulness-based intervention for persons with sickle cell disease: study protocol for a randomized controlled trial.
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Acceptability and Feasibility of a Mindfulness-Based Intervention for Pain Catastrophizing among Persons with Sickle Cell Disease.
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Acceptability of In Utero Hematopoietic Cell Transplantation for Sickle Cell Disease.
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Acute Vaso-Occlusive Pain is Temporally Associated with the Onset of Menstruation in Women with Sickle Cell Disease.
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Acute gastrointestinal vaso-occlusive ischemia in sickle cell disease: CT imaging features and clinical outcome.
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Acute silent cerebral ischemic events in children with sickle cell anemia.
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Adherence to Iron Chelation Therapy with Deferasirox Formulations among Patients with Sickle Cell Disease and β-thalassemia.
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Adherence to hydroxyurea therapy in children with sickle cell anemia.
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Adhesion molecules and hydroxyurea in the pathophysiology of sickle cell disease.
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Adult emergency department patients with sickle cell pain crisis: a learning collaborative model to improve analgesic management.
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Adult emergency department patients with sickle cell pain crisis: results from a quality improvement learning collaborative model to improve analgesic management.
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Allogeneic stem cell transplantation with omidubicel in sickle cell disease.
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Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decreased survival.
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Ambulatory care connections of Medicaid-insured children with sickle cell disease.
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American Society of Hematology 2020 guidelines for sickle cell disease: management of acute and chronic pain.
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Among emergency physicians, use of the term "Sickler" is associated with negative attitudes toward people with sickle cell disease.
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An Interrupted Time Series Analysis of the Dissemination of a Sickle Cell Vaso-Occlusive Episode Treatment Algorithm and a Case Management Referral Form for Individuals With Sickle Cell Disease in the Emergency Department.
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An evaluation of patient-reported outcomes in sickle cell disease within a conceptual model.
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An in vitro system for efficiently evaluating gene therapy approaches to hemoglobinopathies.
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An intervention to increase coping and reduce health care utilization for school-age children and adolescents with sickle cell disease
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An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell disease.
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An unequal burden: poor patient-provider communication and sickle cell disease.
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Angiographic contrast agent-induced acute hemolysis in a patient with hemoglobin SC disease.
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Application of a proactive risk analysis to emergency department sickle cell care.
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Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease.
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Assessment of primary hemostasis by PFA-100 analysis in a tertiary care center.
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Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure.
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Association between somatic growth trajectory and cognitive functioning in young children with sickle cell disease.
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Association of Transition Readiness to Intentional Self-Regulation and Hopeful Future Expectations in Youth With Illness.
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Attitudes toward clinical trials among patients with sickle cell disease.
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Attitudes toward patients with sickle cell disease in a multicenter sample of emergency department providers.
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Awareness and Use of the Sickle Cell Disease Toolbox by Primary Care Providers in North Carolina.
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B-CAM/LU expression and the role of B-CAM/LU activation in binding of low- and high-density red cells to laminin in sickle cell disease.
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Bacteremia in sickle hemoglobinopathies.
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Barriers and facilitators to care for individuals with sickle cell disease in central North Carolina: The emergency department providers' perspective.
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Barriers to Care for Persons With Sickle Cell Disease: The Case Manager's Opportunity to Improve Patient Outcomes.
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Barriers to bone marrow transplantation for sickle cell anemia.
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Basal cell adhesion molecule/lutheran protein. The receptor critical for sickle cell adhesion to laminin.
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Beyond hydroxyurea: new and old drugs in the pipeline for sickle cell disease.
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Blood donation and blood transfusion: special considerations for African Americans.
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Bone marrow transplantation for adolescents and young adults with sickle cell disease: Results of a prospective multicenter pilot study.
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Bone marrow transplantation for sickle cell disease.
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Bone marrow transplantation for sickle cell disease.
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Bone marrow transplantation for sickle cell disease. The United States experience.
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Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects.
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Burden of influenza-related hospitalizations among children with sickle cell disease.
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CE: Understanding the Complications of Sickle Cell Disease.
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CT abdominal imaging findings in patients with sickle cell disease: acute vaso-occlusive crisis, complications, and chronic sequelae.
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CT of Gastrointestinal Vasoocclusive Crisis Complicating Sickle Cell Disease.
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Can subjective pain be inferred from objective physiological data? Evidence from patients with sickle cell disease.
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Cardiopulmonary complications leading to premature deaths in adult patients with sickle cell disease.
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Care of children with sickle cell disease in the emergency department: parent and provider perspectives inform quality improvement efforts.
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Caring for patients with sickle cell disease in North Carolina.
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Cellular adhesion and the endothelium: E-selectin, L-selectin, and pan-selectin inhibitors.
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Cerebral infarction in sickle cell trait.
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Challenges in Shifting Management Responsibility From Parents to Adolescents With Sickle Cell Disease.
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Changes in coping, pain, and activity after cognitive-behavioral training: a randomized clinical trial for pediatric sickle cell disease using smartphones.
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Characterization of the hypercoagulable state in patients with sickle cell disease.
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Childrens' and adolescents' use of diaries for sickle cell pain
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Chromatographic analysis of Hb S for the diagnosis of various sickle cell disorders in Pakistan.
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Chronic granulocytic leukemia in a patient with sickle cell anemia.
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Clinical and metabolomic risk factors associated with rapid renal function decline in sickle cell disease.
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Clinical and sociodemographic factors predict coping styles among adults with sickle cell disease.
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Clinical outcomes of splenectomy in children: report of the splenectomy in congenital hemolytic anemia registry.
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Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases.
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Clonal hematopoiesis in sickle cell disease.
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Coagulation disorders and their cutaneous presentations: Pathophysiology.
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Coexistent Sickle Cell Disease Has No Impact on the Safety or Outcome of Lytic Therapy in Acute Ischemic Stroke: Findings From Get With The Guidelines-Stroke.
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Cognitive functioning and brain magnetic resonance imaging in children with sickle Cell disease. Neuropsychology Committee of the Cooperative Study of Sickle Cell Disease.
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Collaborative multicenter investigation of marrow transplantation for sickle cell disease: current results and future directions.
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Commentary: sickle cell disease.
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Community Health Workers as Support for Sickle Cell Care.
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Comparison of US Federal and Foundation Funding of Research for Sickle Cell Disease and Cystic Fibrosis and Factors Associated With Research Productivity.
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Complications of implantable venous access devices in patients with sickle cell disease.
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Computerized physician order entry improves compliance with a manual exchange transfusion protocol in the pediatric intensive care unit.
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Consensus definition of essential, optimal, and suggested components of a pediatric sickle cell disease center.
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Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness.
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Contraceptive Methods and the Impact of Menstruation on Daily Functioning in Women with Sickle Cell Disease.
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Contribution of sickle cell disease to the occurrence of developmental disabilities: a population-based study.
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Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemia.
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Coping strategies in families of children with sickle cell disease.
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Correlates of successful transition in young adults with sickle cell disease.
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Corticosteroids and increased risk of readmission after acute chest syndrome in children with sickle cell disease.
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Costs and length of stay for patients with and without sickle cell disease after hysterectomy, appendectomy, or knee replacement.
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Creation of a femoral cortical window to facilitate total hip arthroplasty in patients with sickle cell hemoglobinopathies.
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Criterion and convergent validity for 4 measures of pain in a pediatric sickle cell disease population.
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Crizanlizumab and comparators for adults with sickle cell disease: a systematic review and network meta-analysis.
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Curative vs targeted therapy for SCD: does it make more sense to address the root cause than target downstream events?
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Daily mood and stress predict pain, health care use, and work activity in African American adults with sickle-cell disease.
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Daily stress and mood and their association with pain, health-care use, and school activity in adolescents with sickle cell disease.
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Defective release of tissue plasminogen activator in patients with sickle cell anemia.
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Definitions of the phenotypic manifestations of sickle cell disease.
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Dehydration and delayed proton equilibria of red blood cells suspended in isosmotic phosphate buffers. Implications for studies of sickled cells.
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Depression, suicidal ideation, and attempts in black patients with sickle cell disease.
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Design of the silent cerebral infarct transfusion (SIT) trial.
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Design, Synthesis, and Investigation of Novel Nitric Oxide (NO)-Releasing Aromatic Aldehydes as Drug Candidates for the Treatment of Sickle Cell Disease.
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Developing a risk-based composite neurologic outcome for a trial of hydroxyurea in young children with sickle cell disease.
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Development of quality indicators for transition from pediatric to adult care in sickle cell disease: A modified Delphi survey of adult providers.
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Diagnosis of Kikuchi-Fujimoto disease in an 11-year-old girl with fever and sickle cell disease.
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Diastolic dysfunction is an independent risk factor for death in patients with sickle cell disease.
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Differences in pain management between hematologists and hospitalists caring for patients with sickle cell disease hospitalized for vasoocclusive crisis.
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Discontinuing penicillin prophylaxis in children with sickle cell anemia. Prophylactic Penicillin Study II.
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Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions.
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Disrupting the vicious cycle created by NOX activation in sickle erythrocytes exposed to hypoxia/reoxygenation prevents adhesion and vasoocclusion.
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Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program.
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Does Attendance at a Sickle Cell Educational Conference Improve Clinician Knowledge and Attitude Toward Patients with Sickle Cell Disease?
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ELIPSIS: developing tools to better understand VOC in SCD.
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Early Initiation of Sub-Anesthetic Ketamine Infusion in Adults with Vaso-Occlusive Crises Is Associated with Greater Reduction in Sickle Cell Pain Intensity: A Single Center's Experience.
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Eccrine Chromhidrosis in an Adolescent with Sickle Cell Disease.
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Echocardiography-derived tricuspid regurgitant jet velocity is an important marker for the progression of sickle-cell disease.
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Effect of Free Dental Services on Individuals with Sickle Cell Disease.
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Effect of Poloxamer 188 vs Placebo on Painful Vaso-Occlusive Episodes in Children and Adults With Sickle Cell Disease: A Randomized Clinical Trial.
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Effect of myeloablative bone marrow transplantation on growth in children with sickle cell anaemia: results of the multicenter study of haematopoietic cell transplantation for sickle cell anaemia.
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Effect of propranolol as antiadhesive therapy in sickle cell disease.
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Effective Recruitment Strategies for a Sickle Cell Patient Registry Across Sites from the Sickle Cell Disease Implementation Consortium (SCDIC).
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Effects of hydroxyurea treatment for patients with hemoglobin SC disease.
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Effects of red blood cell (RBC) transfusion on sickle cell disease recipient plasma and RBC metabolism.
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Effects of repleting organic phosphates in banked erythrocytes on plasma metabolites and vasoactive mediators after red cell exchange transfusion in sickle cell disease.
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Efficacy and safety of the Gardos channel blocker, senicapoc (ICA-17043), in patients with sickle cell anemia.
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Efficient and specific repair of sickle beta-globin RNA by trans-splicing ribozymes.
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Electroretinographic findings in sickle cell retinopathy.
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Emergency Department (ED), ED Observation, Day Hospital, and Hospital Admissions for Adults with Sickle Cell Disease.
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Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS), a focus group and decision support tool development project.
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Emergency department analgesia without narcotics for adults with acute sickle cell pain crisis: case reports and review of crisis management.
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Emergency department management of acute pain episodes in sickle cell disease.
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Emergency department visits and hospitalizations among patients with sickle cell disease in illinois, 2016-2020.
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Emergency provider analgesic practices and attitudes toward patients with sickle cell disease.
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Emotional reactions to pain predict psychological distress in adult patients with Sickle Cell Disease (SCD).
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Enalapril and hydroxyurea therapy for children with sickle nephropathy.
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End points for sickle cell disease clinical trials: patient-reported outcomes, pain, and the brain.
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Enuresis in children and adolescents with sickle cell anaemia is more frequent and substantially different from the general population.
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Epinephrine acts through erythroid signaling pathways to activate sickle cell adhesion to endothelium via LW-alphavbeta3 interactions.
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Epinephrine-induced activation of LW-mediated sickle cell adhesion and vaso-occlusion in vivo.
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Erythrocyte adhesion in sickle cell disease.
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Erythrocyte adhesion receptors: blood group antigens and related molecules.
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Erythrocyte plasma membrane-bound ERK1/2 activation promotes ICAM-4-mediated sickle red cell adhesion to endothelium.
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Evaluation of a Sickle Cell Disease Educational Website for Emergency Providers.
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Evaluation of a train-the-trainer workshop on sickle cell disease for ED providers.
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Evaluation of partial and total splenectomy in children with sickle cell disease using an Internet-based registry.
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Evidence gaps in the management of sickle cell disease: A summary of needed research.
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Exploring Emergency Department Provider Experiences With and Perceptions of Weight-Based Versus Individualized Vaso-Occlusive Treatment Protocols in Sickle Cell Disease.
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Factors associated with survival in a contemporary adult sickle cell disease cohort.
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Family functioning, neurocognitive functioning, and behavior problems in children with sickle cell disease.
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Fast measurement of blood T1 in the human jugular vein at 3 Tesla.
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Fatal small-bowel necrosis and pulmonary hypertension in sickle cell disease.
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Fatigue in Children With Sickle Cell Disease: Association With Neurocognitive and Social-Emotional Functioning and Quality of Life.
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Fear of movement (kinesiophobia), pain, and psychopathology in patients with sickle cell disease.
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Feasibility of implementing mobile technology-delivered mental health treatment in routine adult sickle cell disease care.
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Fertility challenges for women with sickle cell disease.
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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
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Fludarabine-based nonmyeloablative stem cell transplantation for sickle cell disease with and without renal failure: clinical outcome and pharmacokinetics.
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Focus groups with African American adolescents: enhancing recruitment and retention in intervention studies
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Follow-up of coping skills training in adults with sickle cell disease: analysis of daily pain and coping practice diaries.
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Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients.
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Genetic Modifiers of Sickle Cell Disease.
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Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study.
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Genetic polymorphisms associated with priapism in sickle cell disease.
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Genetics and ethics: reaffirming the tragic vision.
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Genitourinary complications of sickle cell disease.
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Glycemic monitoring in diabetics with sickle cell plus beta-thalassemia hemoglobinopathy.
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Glycosylated hemoglobin levels in a benign form of sickle cell anemia in Saudi Arabia.
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Growing up with sickle cell disease: a pilot study of a transition program for adolescents with sickle cell disease.
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Gαs proteins activate p72(Syk) and p60-c-Src tyrosine kinases to mediate sickle red blood cell adhesion to endothelium via LW-αvβ3 and CD44-CD44 interactions.
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HPLC measurement, blood distribution, and pharmacokinetics of oral clotrimazole, potentially useful antisickling agent.
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Health related quality of life in sickle cell disease: just scratching the surface.
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Health-related quality of life in children with sickle cell anemia: impact of blood transfusion therapy.
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Health-related quality of life in sickle cell disease: past, present, and future.
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Hematologic outcomes after total splenectomy and partial splenectomy for congenital hemolytic anemia.
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Heme redox properties of S-nitrosated hemoglobin A0 and hemoglobin S: implications for interactions of nitric oxide with normal and sickle red blood cells.
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Hemorrhagic Stroke in Children and Adults With Sickle Cell Anemia: The Post-STOP Cohort.
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Hemostatic activation in a chemically induced rat model of severe hemolysis and thrombosis.
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Hepatic biloma complicating sickle cell disease. A case report and a review of the literature.
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High rates of recurrent biliary tract obstruction in children with sickle cell disease.
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Homozygous sickle cell disease and cystic fibrosis in an adolescent.
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Hybrid Statistical and Mechanistic Mathematical Model Guides Mobile Health Intervention for Chronic Pain.
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Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority trial.
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Hydroxyurea for Sickle Cell Disease: Now Is the Time!
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Hydroxyurea for sickle cell disease: a systematic review for efficacy and toxicity in children.
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Hydroxyurea for the treatment of sickle cell disease.
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Hydroxyurea for the treatment of sickle cell disease: efficacy, barriers, toxicity, and management in children.
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Hydroxyurea: specific therapy for sickle cell anemia?
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IMPROVE trial: a randomized controlled trial of patient-controlled analgesia for sickle cell painful episodes: rationale, design challenges, initial experience, and recommendations for future studies.
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Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.
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Identifying Social-Behavioral Health Needs of Adults with Sickle Cell Disease in the Emergency Department.
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Identifying barriers to evidence-based care for sickle cell disease: results from the Sickle Cell Disease Implementation Consortium cross-sectional survey of healthcare providers in the USA.
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Impact of Depression in Sickle Cell Disease Hospitalization-Related Outcomes: An Analysis of the National Inpatient Sample (NIS).
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Impact of Medicaid expansion on access and healthcare among individuals with sickle cell disease.
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Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report. Multicenter investigation of bone marrow transplantation for sickle cell disease.
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Impact of hydroxyurea on perioperative management and outcomes in children with sickle cell anemia.
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Implantation of penile prostheses in patients impotent after priapism.
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Implementation of an Emergency Department Screening and Care Management Referral Process for Patients With Sickle Cell Disease.
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Implementation science research for the scale-up of evidence-based interventions for sickle cell disease in africa: a commentary.
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Improving Inpatient Care for Individuals with Sickle Cell Disease Using the Project ECHO Model.
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Improving Quality of Care for Sickle Cell Patients in the Pediatric Emergency Department.
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Improving care for children with sickle cell disease/acute chest syndrome.
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Improving the Care of Individuals With Sickle Cell Disease in the Emergency Department Using a Quality Improvement Framework: The Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS).
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Improving the Quality of Care for Adolescents and Adults With Sickle Cell Disease-It's a Long Road.
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Incidental findings on brain magnetic resonance imaging of children with sickle cell disease.
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Increased prevalence of potential right-to-left shunting in children with sickle cell anaemia and stroke.
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Indications and Results of HLA-Identical Sibling Hematopoietic Cell Transplantation for Sickle Cell Disease.
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Influence of penicillin prophylaxis on antimicrobial resistance in nasopharyngeal S. pneumoniae among children with sickle cell anemia. The Ancillary Nasopharyngeal Culture Study of Prophylactic Penicillin Study II.
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Initial Evaluation of the Pediatric PROMIS® Health Domains in Children and Adolescents With Sickle Cell Disease.
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Intentional and unintentional nonadherence to hydroxyurea among people with sickle cell disease: a qualitative study.
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Interval decline in hemoglobin A is associated with annual clinical event rate in sickle cell anemia patients receiving maintenance apheresis RBC exchange.
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Intranasal fentanyl improves time to analgesic delivery in sickle cell pain crises.
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Introduction to a symposium on sickle cell anemia: current results of comprehensive care and the evolving role of bone marrow transplantation.
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Invasive pneumococcal infections in children with sickle cell disease in the era of penicillin prophylaxis, antibiotic resistance, and 23-valent pneumococcal polysaccharide vaccination.
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Inverse correlation between cerebral blood flow measured by continuous arterial spin-labeling (CASL) MRI and neurocognitive function in children with sickle cell anemia (SCA).
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Is low dose hydroxyurea the solution to the global epidemic of sickle cell disease?
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Ischemic colitis in a young adult during sickle cell crisis: case report and review.
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It's Time to Provide Evidence-Based Care to Individuals with Sickle Cell Disease: A Call to Action.
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Kidney biopsy findings in children with sickle cell disease: a Midwest Pediatric Nephrology Consortium study.
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Kikuchi-Fugimoto's disease in sickle cell disease: report of 2 cases.
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Knowledge gaps in reproductive and sexual health in girls and women with sickle cell disease.
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LW protein: a promiscuous integrin receptor activated by adrenergic signaling.
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Laboratory profile of sickle cell disease: a cross-sectional analysis. The Cooperative Study of Sickle Cell Disease.
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Lack of Duffy antigen expression is associated with organ damage in patients with sickle cell disease.
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Language processing deficits in sickle cell disease in young school-age children.
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Laparoscopic cholecystectomy in young patients with sickle hemoglobinopathies.
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Letter to the Editor: Physicians' Opinions of COVID-19 Ambulatory Care Constraints: A Survey of Sickle Cell Clinicians.
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Living with sickle cell disease: traversing 'race' and identity.
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Long-term biological effects in sickle cell disease: insights from a post-crizanlizumab study.
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Longitudinal study of glomerular hyperfiltration in adults with sickle cell anemia: a multicenter pooled analysis.
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Low cobalamin levels in African Americans with and without sickle cell disease.
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MEK inhibitors, novel anti-adhesive molecules, reduce sickle red blood cell adhesion in vitro and in vivo, and vasoocclusion in vivo.
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MEK1/2 inhibitors reverse acute vascular occlusion in mouse models of sickle cell disease.
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MR features of soft-tissue abnormalities due to acute marrow infarction in five children with sickle cell disease.
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MYH9 and APOL1 are both associated with sickle cell disease nephropathy.
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Management of Sickle Cell Disease in Children.
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Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.
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Matched-related donor transplantation for sickle cell disease: report from the Center for International Blood and Transplant Research.
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Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans.
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Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients.
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Mn porphyrins as a novel treatment targeting sickle cell NOXs to reverse and prevent acute vaso-occlusion in vivo.
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Mobile health intervention for youth with sickle cell disease: Impact on adherence, disease knowledge, and quality of life.
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Moderate chronic pain, weight and dietary intake in African-American adult patients with sickle cell disease.
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Monthly sulfadoxine/pyrimethamine-amodiaquine or dihydroartemisinin-piperaquine as malaria chemoprevention in young Kenyan children with sickle cell anemia: A randomized controlled trial.
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Morbidity and mortality in chronically transfused subjects with thalassemia and sickle cell disease: A report from the multi-center study of iron overload.
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Morbidity associated with sickle cell disease in pregnancy.
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Multidisciplinary care results in similar maternal and perinatal mortality rates for women with and without SCD in a low-resource setting.
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Myeloid neoplasms in the setting of sickle cell disease: an intrinsic association with the underlying condition rather than a coincidence; report of 4 cases and review of the literature.
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NIH consensus development statement on hydroxyurea treatment for sickle cell disease.
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National Institutes of Health Consensus Development Conference statement: hydroxyurea treatment for sickle cell disease.
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Neurocognitive development of young children with sickle cell disease through three years of age.
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Neurocognitive testing and functioning in adults sickle cell disease.
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Neurodevelopmental Screening in Toddlers and Early Preschoolers with Sickle Cell Disease
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Neurologic complications after allogeneic marrow transplantation for sickle cell anemia.
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Neuropsychologic performance in school-aged children with sickle cell disease: a report from the Cooperative Study of Sickle Cell Disease.
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Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia.
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New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell disease.
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Newborn screening for sickle cell disease and other hemoglobinopathies. Techniques' comparison and report of the North Carolina experience.
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Nitric oxide loading reduces sickle red cell adhesion and vaso-occlusion in vivo.
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Novel epinephrine and cyclic AMP-mediated activation of BCAM/Lu-dependent sickle (SS) RBC adhesion.
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Opioid management and dependency among adult patients with sickle cell disease.
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Optimizing management of sickle cell disease in patients undergoing surgery.
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Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trial.
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Osteomyelitis in sickle cell disease: You know it when you see it?
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Osteomyelitis. Common causes and treatment recommendations.
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Outcomes of acute chest syndrome in adult patients with sickle cell disease: predictors of mortality.
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Outcomes of inpatients with and without sickle cell disease after high-volume surgical procedures.
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Oxygen radical inhibition of nitric oxide-dependent vascular function in sickle cell disease.
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Pain and other non-neurological adverse events in children with sickle cell anemia and previous stroke who received hydroxyurea and phlebotomy or chronic transfusions and chelation: results from the SWiTCH clinical trial.
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Parent education and biologic factors influence on cognition in sickle cell anemia.
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Parental substance abuse, reports of chronic pain and coping in adult patients with sickle cell disease.
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Patent foramen ovale in adults with sickle cell disease and stroke.
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Pathological effects of sickle cell anemia on the pulp.
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Patient Perspectives of Sickle Cell Management in the Emergency Department.
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Patient-Centered eHealth Interventions for Children, Adolescents, and Adults With Sickle Cell Disease: Systematic Review.
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Patient-reported neurocognitive symptoms influence instrumental activities of daily living in sickle cell disease.
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Patient-reported outcomes in sickle cell disease and association with clinical and psychosocial factors: Report from the sickle cell disease implementation consortium.
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Patients welcome the Sickle Cell Disease Mobile Application to Record Symptoms via Technology (SMART).
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Pediatric Neurodevelopmental Delays in Children 0 to 5 Years of Age With Sickle Cell Disease: A Systematic Literature Review.
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Pediatric hematology providers' contraceptive practices for female adolescents and young adults with sickle cell disease: A national survey.
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Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease.
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Perceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell disease.
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Pericardial effusion in sickle cell anemia: a rare problem.
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Perioperative management for orthopaedic patients with sickle cell anaemia.
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Personalized Reminders Increase Screening for Stroke Risk in Children with Sickle Cell Anemia.
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Perspectives of individuals with sickle cell disease on barriers to care.
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Pharmacokinetics and analgesic effects of methadone in children and adults with sickle cell disease.
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Pharmacokinetics and bioequivalence of a liquid formulation of hydroxyurea in children with sickle cell anemia.
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Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease.
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Phase 1 study of the E-selectin inhibitor GMI 1070 in patients with sickle cell anemia.
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Placenta growth factor in sickle cell disease: association with hemolysis and inflammation.
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Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis.
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Potential role for statins in sickle cell disease.
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Pregnancy associated with both insulin-dependent diabetes mellitus and sickle cell disease. A report of two cases.
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Pregnancy outcomes with hydroxyurea use in women with sickle cell disease.
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Prevalence and clinical correlates of glomerulopathy in children with sickle cell disease.
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Prevalence and risk factors of elevated pulmonary artery pressures in children with sickle cell disease.
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Preventive Care Delivery to Young Children With Sickle Cell Disease.
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Priapism: etiology, treatment, and results in series of 35 presentations.
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Primary Care Providers' Comfort Levels in Caring for Patients with Sickle Cell Disease.
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Primary hemorrhagic stroke in children with sickle cell disease is associated with recent transfusion and use of corticosteroids.
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Primary prevention of ischemic stroke: A statement for healthcare professionals from the Stroke Council of the American Heart Association.
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Primary prevention of ischemic stroke: A statement for healthcare professionals from the Stroke Council of the American Heart Association.
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Principles and problems of transfusion in sickle cell disease.
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Prolongation of QTc intervals and risk of death among patients with sickle cell disease.
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Promoting equity: developing quality measures for sickle cell disease.
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Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial.
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Protrusio acetabuli in sickle-cell anemia.
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Psychological adjustment of adults with sickle cell anemia: stability over 20 months, correlates, and predictors.
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Psychological adjustment of children with sickle cell disease: stability and change over a 10-month period.
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Psychological adjustment of mothers of children and adolescents with sickle cell disease: the role of stress, coping methods, and family functioning.
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Psychosocial Burden of Childhood Sickle Cell Disease on Caregivers in Kenya.
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Publication of data collection forms from NHLBI funded sickle cell disease implementation consortium (SCDIC) registry.
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Pulmonary hypertension and nitric oxide depletion in sickle cell disease.
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Pulmonary hypertension associated with sickle cell disease: clinical and laboratory endpoints and disease outcomes.
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Pulmonary, gonadal, and central nervous system status after bone marrow transplantation for sickle cell disease.
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Pyridoxamine: another vitamin for sickle cell disease?
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Quality improvement process in a sickle cell infusion center.
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Quantification of macular ischaemia in sickle cell retinopathy.
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Quantification of whole-brain oxygenation extraction fraction and cerebral metabolic rate of oxygen consumption in adults with sickle cell anemia using individual T2 -based oxygenation calibrations.
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Quantitative microscopy and nanoscopy of sickle red blood cells performed by wide field digital interferometry.
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RNA aptamer therapy for vaso-occlusion in sickle cell disease.
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RNA sequencing of isolated cell populations expressing human APOL1 G2 risk variant reveals molecular correlates of sickle cell nephropathy in zebrafish podocytes.
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Randomized controlled trial of sildenafil for preventing recurrent ischemic priapism in sickle cell disease.
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Randomized phase 2 study of GMI-1070 in SCD: reduction in time to resolution of vaso-occlusive events and decreased opioid use.
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Rapid decline in estimated glomerular filtration rate in sickle cell anemia: results of a multicenter pooled analysis.
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Real-world effectiveness of voxelotor for treating sickle cell disease in the US: a large claims data analysis.
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Red blood cell surface adhesion molecules: their possible roles in normal human physiology and disease.
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Red cell antigens as functional molecules and obstacles to transfusion.
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Regulation of tissue plasminogen activator in sickle cell anemia.
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Reimmunization to pneumococcus in patients with sickle cell disease: do they or don't they respond?
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Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease.
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Relationships between Somatic Growth and Cognitive Functioning in Children with Sickle Cell Disease
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Religiosity/spirituality and pain in patients with sickle cell disease.
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Reply to comment on: Pharmacokinetics and analgesic effects of methadone in children and adults with sickle cell disease.
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Reply: Practice guideline for pulmonary hypertension in sickle cell: direct evidence needed before universal adoption.
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Reproducibility of detecting silent cerebral infarcts in pediatric sickle cell anemia.
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Respiratory syncytial virus and seasonal influenza cause similar illnesses in children with sickle cell disease.
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Response to "The need for logical application-based extensions in sickle cell disease research findings to changing lives in the ethnic context".
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Responses of normal and sickle cell hemoglobin to S-nitroscysteine: implications for therapeutic applications of NO in treatment of sickle cell disease.
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Responsiveness of PROMIS® Pediatric Measures to Hospitalizations for Sickle Pain and Subsequent Recovery.
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Results and complications of total hip arthroplasties in patients with sickle-cell hemoglobinopathies. Role of cementless components.
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Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia.
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Ribozyme-mediated repair of sickle beta-globin mRNAs in erythrocyte precursors.
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Role and regulation of sickle red cell interactions with other cells: ICAM-4 and other adhesion receptors.
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Role of Rap1 in promoting sickle red blood cell adhesion to laminin via BCAM/LU.
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Role of adhesion molecules and vascular endothelium in the pathogenesis of sickle cell disease.
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Role of child and maternal processes in the psychological adjustment of children with sickle cell disease.
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Safe and Effective In Vivo Targeting and Gene Editing in Hematopoietic Stem Cells: Strategies for Accelerating Development.
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Safety of an ED High-Dose Opioid Protocol for Sickle Cell Disease Pain.
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Secondhand Smoke Is an Important Modifiable Risk Factor in Sickle Cell Disease: A Review of the Current Literature and Areas for Future Research.
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Secondhand smoke is associated with more frequent hospitalizations in children with sickle cell disease.
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Segmentation and quantification of pulmonary artery for noninvasive CT assessment of sickle cell secondary pulmonary hypertension.
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Sensitization to Acute Procedural Pain in Pediatric Sickle Cell Disease: Modulation by Painful Vaso-occlusive Episodes, Age, and Endothelin-1
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Serotype-specific immunoglobulin G antibody responses to pneumococcal polysaccharide vaccine in children with sickle cell anemia: effects of continued penicillin prophylaxis.
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Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts.
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Severe Mycoplasma pneumonia in three sisters with sickle cell disease.
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Severe Pain Profiles and Associated Sociodemographic and Clinical Characteristics in Individuals With Sickle Cell Disease.
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Severe Persistent Pain and Inflammatory Biomarkers in Sickle Cell Disease: An Exploratory Study.
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Severe pandemic H1N1 and seasonal influenza in children and young adults with sickle cell disease.
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Sevuparin binds to multiple adhesive ligands and reduces sickle red blood cell-induced vaso-occlusion.
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Sex-based differences in the manifestations and complications of sickle cell disease: Report from the Sickle Cell Disease Implementation Consortium.
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Shared Decision-Making in Hematopoietic Stem Cell Transplantation for Sickle Cell Disease.
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Shift in Emergency Department Provider Attitudes Toward Patients With Sickle Cell Disease.
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Should modulation of p50 be a therapeutic target in the critically ill?
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Sickle Cell Disease: A Review of Nonpharmacological Approaches for Pain.
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Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients.
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Sickle cell disease complications: Prevalence and resource utilization.
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Sickle cell disease in children and adolescents: the relation of child and parent pain coping strategies to adjustment.
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Sickle cell disease is associated with iron mediated hypercoagulability.
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Sickle cell disease management in the emergency department: what every emergency nurse should know.
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Sickle cell disease pain in children and adolescents: change in pain frequency and coping strategies over time.
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Sickle cell disease pain: relation of coping strategies to adjustment.
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Sickle cell disease patients' perceptions of emergency department pain management.
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Sickle cell disease.
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Sickle cell disease: an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation.
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Sickle cell vaso-occlusive pain crisis in adults: alternative strategies for management in the emergency department.
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Sickle erythrocytes target cytotoxics to hypoxic tumor microvessels and potentiate a tumoricidal response.
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Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.
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Sickle red cells induce adhesion of lymphocytes and monocytes to endothelium.
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Sickle-Cell Disease Co-Management, Health Care Utilization, and Hydroxyurea Use.
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Significant responses to platinum-based chemotherapy in renal medullary carcinoma.
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Silent cerebral infarct definitions and full-scale IQ loss in children with sickle cell anemia.
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Silent cerebral infarction, income, and grade retention among students with sickle cell anemia.
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Skin and nail changes in children with sickle cell anemia receiving hydroxyurea therapy.
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Social and Behavioral Factors in Sickle Cell Disease: Employment Predicts Decreased Health Care Utilization.
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Socioeconomic Disparities and Risk Factors in Patients Presenting With Ischemic Priapism: A Multi-Institutional Study.
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Somatization in the conceptualization of sickle cell disease.
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Splenectomy in sickle-cell disease.
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Stability and change in the psychological adjustment of mothers of children and adolescents with cystic fibrosis and sickle cell disease.
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Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia.
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Stem-cell transplantation for sickle cell disease.
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Stigma of Sickle Cell Disease: A Systematic Review.
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Subcutaneous panniculitis-like T-cell lymphoma in a 25-year-old male patient with sickle cell disease.
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Successful pulmonary thromboendarterectomy in two patients with sickle cell disease.
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Successful surgical outcome in children with sickle hemoglobinopathies: the Duke University experience.
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Surgical and obstetric outcomes in adults with sickle cell disease.
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Symptomatic Avascular Necrosis: An Understudied Risk Factor for Acute Care Utilization by Patients with SCD.
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Systematic Review of the Impact of Transition Interventions for Adolescents With Chronic Illness on Transfer From Pediatric to Adult Healthcare.
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Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease.
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Tackling adherence in sickle cell disease with mHealth.
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Technologies for global health.
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Telehealth acceptability and opioid prescribing patterns of providers of painful chronic diseases during the COVID-19 pandemic: A survey of sickle cell providers.
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The Association between Educational Attainment and Patterns of Emergency Department Utilization among Adults with Sickle Cell Disease.
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The Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS): reliability and validity.
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The Prevalence of Uterine Fibroids in African American Women with Hemoglobin SS Sickle Cell Disease as Determined by Pelvic Magnetic Resonance Imaging.
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The Sickle Cell Disease Ontology: enabling universal sickle cell-based knowledge representation.
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The association of optimism and perceived discrimination with health care utilization in adults with sickle cell disease.
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The association of oral hydroxyurea therapy with improved cognitive functioning in sickle cell disease
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The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia.
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The epidemiology, evaluation and treatment of stroke in adults with sickle cell disease.
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The excess burden of stroke in hospitalized adults with sickle cell disease.
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The genomic analysis of erythrocyte microRNA expression in sickle cell diseases.
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The impact of race and disease on sickle cell patient wait times in the emergency department.
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The impact of vaso-occlusive crises and disease severity on quality of life and productivity among patients with sickle cell disease in the US.
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The lung in sickle cell disease.
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The oral ferroportin inhibitor vamifeport improves hemodynamics in a mouse model of sickle cell disease.
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The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.
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The sickle cell disease implementation consortium: Translating evidence-based guidelines into practice for sickle cell disease.
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Therapeutic strategies for sickle cell disease: towards a multi-agent approach.
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Third trimester and early postpartum period of pregnancy have the greatest risk for ACS in women with SCD.
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Thrombospondin-1 gene polymorphism is associated with estimated pulmonary artery pressure in patients with sickle cell anemia.
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Transcranial Doppler screening of Medicaid-insured children with sickle cell disease.
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Transcutaneous electrical nerve stimulation treatment of sickle cell pain crises.
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Transfusion management in sickle cell disease.
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Transfusion practices for patients with sickle cell disease at a major academic medical center.
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Transfusion-transmitted babesiosis: achieving successful mitigation while balancing cost and donor loss.
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Transient open-angle glaucoma associated with sickle cell trait: report of 4 cases.
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Transition to adult care in sickle cell disease: A longitudinal study of clinical characteristics and disease severity.
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Transitioning Adolescents With Sickle Cell Disease From Pediatric to Adult Care: Results From a New Survey of Health Care Professionals.
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Transplantation of a child with sickle cell anemia with an unrelated cord blood unit after reduced intensity conditioning.
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Travelers with sickle cell disease.
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Treatment patterns and economic burden of sickle-cell disease patients prescribed hydroxyurea: a retrospective claims-based study.
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Trends in Sickle Cell Disease-related Priapism in U.S. Children's Hospitals.
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Trial design of comparing patient-specific versus weight-based protocols to treat vaso-occlusive episodes in sickle cell disease (COMPARE-VOE).
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Twelve tips for teaching a comprehensive disease-focused course with a global perspective: A sickle cell disease example.
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Umbilical cord blood transplantation for children with thalassemia and sickle cell disease.
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Understanding and meeting the hospitalist's challenge: caring for adults with sickle cell disease.
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Understanding patient preferences for femoral central venous catheterization among patients with sickle cell disease.
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Understanding patterns and correlates of daily pain using the Sickle cell disease Mobile Application to Record Symptoms via Technology (SMART).
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Unrelated cord blood transplantation in children with sickle cell disease: review of four-center experience.
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Urgency of emergency department visits by children with sickle cell disease: a comparison of 3 chronic conditions.
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Usability and Feasibility of an mHealth Intervention for Monitoring and Managing Pain Symptoms in Sickle Cell Disease: The Sickle Cell Disease Mobile Application to Record Symptoms via Technology (SMART).
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Use of Handheld Wireless Technology For a Home-based Sickle Cell Pain Management Protocol
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Use of Mobile Health Apps and Wearable Technology to Assess Changes and Predict Pain During Treatment of Acute Pain in Sickle Cell Disease: Feasibility Study.
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Use of the Spiritual Development Framework in Conducting Spirituality and Health Research with Adolescents.
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Use of the tourniquet during surgery in patients with sickle cell hemoglobinopathies.
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Utility of the Montreal Cognitive Assessment as a Screening Test for Neurocognitive Dysfunction in Adults with Sickle Cell Disease.
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Validation of a novel point of care testing device for sickle cell disease.
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Vaso-occlusive crises and costs of sickle cell disease in patients with commercial, Medicaid, and Medicare insurance - the perspective of private and public payers.
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What does it mean to be affiliated with care?: Delphi consensus on the definition of "unaffiliation" and "specialist" in sickle cell disease.
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Will submandibular TCD prevent stroke in children with sickle cell anemia?
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Would you terminate a pregnancy affected by sickle cell disease? Analysis of views of patients in Cameroon.
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[Formula: see text]Executive functioning and health-related quality of life in pediatric sickle cell disease.
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beta(2)-Adrenergic receptor and adenylate cyclase gene polymorphisms affect sickle red cell adhesion.
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microRNA miR-144 modulates oxidative stress tolerance and associates with anemia severity in sickle cell disease.
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Keywords of People
-
Kayle, Mariam,
Assistant Professor in the School of Nursing,
School of Nursing
-
Myers, John,
Instructor in the School of Nursing,
School of Nursing
-
Oyedeji, Charity,
Assistant Professor of Medicine,
Medicine, Hematology
-
Palmer, Gregory M.,
Associate Professor of Radiation Oncology,
Radiation Oncology
-
Reed, Shelby Derene,
Professor in Population Health Sciences,
Duke Science & Society
-
Wax, Adam P.,
Professor of Biomedical Engineering,
Biomedical Engineering
-
Zennadi, Rahima,
Associate Professor in Medicine,
Pathology