Building partnerships to target sickle cell anemia in Africa
A prospective newborn screening and treatment program for sickle cell anemia in Luanda, Angola
Darbepoetin-alfa and intravenous iron administration after autologous hematopoietic stem cell transplantation: A prospective multicenter randomized trial
The changing incidence of primary central nervous system lymphoma is driven primarily by the changing incidence in young and middle-aged men and differs from time trends in systemic diffuse large B-cell non-Hodgkin's lymphoma
Decreased survival in normal karyotype AML with single-nucleotide polymorphisms in genes encoding the AraC metabolizing enzymes cytidine deaminase and 5′-nucleotidase
Thrombin generation and procoagulant phospholipids in patients with essential thrombocythemia and reactive thrombocytosis
World Health Organization-defined classification of myeloproliferative neoplasms: Morphological reproducibility and clinical correlations—The Danish experience
Safety and efficacy of upfront plerixafor + G-CSF versus placebo + G-CSF for mobilization of CD34+ hematopoietic progenitor cells in patients ≥60 and <60 years of age with non-Hodgkin's lymphoma or multiple myeloma
Significance of deeper molecular responses in patients with chronic myeloid leukemia in early chronic phase treated with tyrosine kinase inhibitors
The Canadian “National Program for hemophilia mutation testing” database: A ten-year review
Hyperimmune globulins and same-day thrombotic adverse events as recorded in a large healthcare database during 2008–2011
Thrombopoietin levels in patients with disorders of platelet production: Diagnostic potential and utility in predicting response to TPO Receptor agonists
Transferrin-immune complex disease: A potentially overlooked gammopathy mediated by IgM and IgG
Associations between allergies and risk of hematologic malignancies: Results from the VITamins and lifestyle cohort study
TET2 mutations, myelodysplastic features, and a distinct immunoprofile characterize blastic plasmacytoid dendritic cell neoplasm in the bone marrow
The lymphocyte to monocyte ratio improves the IPI-risk definition of diffuse large B-cell lymphoma when rituximab is added to chemotherapy
Efficacy and safety of deferasirox compared with deferoxamine in sickle cell disease: Two-year results including pharmacokinetics and concomitant hydroxyurea
Outcomes of elderly de novo acute myeloid leukemia treated by a risk-adapted approach based on age, comorbidity, and performance status
Mantle cell lymphoma: 2013 Update on diagnosis, risk-stratification, and clinical management
Diagnosis of pyrimidine 5′-nucleotidase deficiency suspected from a blood film
Blue toes and a new pair of shoes—Challenges in diagnosis and treatment of acute myelogenous leukemia
Intracellular and extracellular immunoglobulin crystals assuming a multitude of geometric shapes in an IgG-λ plasma cell neoplasm
Fatal neurological side-effects with necrosis of spinal cord following nelarabine treatment in a child with relapsed T-cell acute lymphoblastic leukemia
VARIATION IN THE TREATMENT OF STROKE IN SICKLE CELL DISEASE: A SURVEY OF PROVIDERS
PITFALLS OF USING ADMINISTRATIVE DATA SETS TO DESCRIBE CLINICAL CARE IN SICKLE CELL DISEASE
REDUCING 30 DAY READMISSION RATES IN CHILDREN AND YOUNG ADULTS WITH SICKLE CELL DISEASE
NURSES' ATTITUDES TOWARDS PATIENTS WITH SICKLE CELL DISEASE
EVALUATION OF THE PEDIATRIC PROMIS HEALTH DOMAINS IN CHILDREN AND ADOLESCENTS WITH SICKLE CELL DISEASE (SCD)-COMPARISON TO PEDS QL SCALE SCORES
EVIDENCE OF ALTERED PAIN PROCESSING IN ADOLESCENTS AND YOUNG ADULTS WITH SICKLE CELL DISEASE
UTILIZATION AND OUTCOME OF BONE MARROW TRANSPLANTATION IN CHILDREN WITH SICKLE CELL DISEASE: A PEDIATRIC HEALTH INFORMATION SYSTEM DATABASE ANALYSIS
EDUCATING PATIENTS AND PHYSICIANS ON HEMATOPOIETIC CELL TRANSPLANTATION AS A VIABLE TREATMENT OPTION FOR SICKLE CELL DISEASE
DECISIONS ABOUT TRANSPLANT IN PEDIATRIC SICKLE CELL DISEASE: ARE FAMILIES AND PROVIDERS ON THE SAME PAGE?
IMPROVED ANEMIA, ORGANOMEGALY AND SUSTAINED FETAL HEMOGLOBIN INDUCTION WITHIN AGING TR2/TR4 OVEREXPRESSING HUMANIZED SICKLE CELL MICE.
EVALUATION OF THE IMPACT OF A WEB-BASED EDUCATIONAL TOOL ON AWARENESS OF NEWBORN SCREENING AND CARRIER TESTING
A NEW PLAY ON AN OLD WAY: SICKLE CELL TRAIT EDUCATION THAT REALLY WORKS
A FOUR YEAR PERSPECTIVE ON THE ISSUES AND CONCERNS OF MANDATORY SICKLE CELL TRAIT TESTING IN COLLEGE ATHLETES
QUALITATIVE STUDY OF THE APPLICABILITY AND FEASIBILITY OF A WEB-BASED PAIN DIARY FOR ADOLESCENTS AND YOUNG ADULTS WITH SICKLE CELL DISEASE
ASSESSING HEALTH MAINTENANCE FOR PEDIATRIC PATIENTS WITH SICKLE CELL DISEASE CHART REVIEW OF PEDIATRIC SICKLE CELL PATIENTS AT UNIVERSITY OF ILLINOIS HOSPITAL
IMPROVING QUALITY OF CARE FOR SICKLE CELL PATIENTS IN THE PEDIATRIC EMERGENCY DEPARTMENT
DEVELOPMENT OF PRIMARY CARE PROVIDER MEDICAL HOMES FOR PATIENTS WITH SICKLE CELL DISEASE
MATERNAL AND PERINATAL OUTCOME IN PREGNANT WOMEN WITH SICKLE CELL DISEASE AND RISK ASSESSMENT OF NEAR MISS OR MATERNAL DEATH: PROSPECTIVE STUDY OF PROJECT ANINHA IN MINAS GERAIS, BRAZIL.
ISCHEMIC STROKE PREVENTION IN SICKLE CELL DISEASE: DATA FROM BELO HORIZONTE BLOOD CENTER, BRAZIL
A SIMPLE, RAPID, LOW-COST DIAGNOSTIC TEST FOR SICKLE CELL DISEASE
EVIDENCE OF ALTERED PAIN PROCESSING IN ADOLESCENTS AND YOUNG ADULTS WITH SICKLE CELL DISEASE
CHOOSING OPIOID MANAGEMENT FOR PAIN AND ANALYZING ACS RATES EQUALLY (COMPARE)
CLINICALLY MEANINGFUL MEASUREMENT OF PAIN IN CHILDREN WITH SICKLE CELL DISEASE
THE DEVELOPMENT AND VALIDATION OF THE CHILDREN'S ACUTE PAIN-FUNCTIONAL ABILITY QUESTIONNAIRE
INDIVIDUALIZED PAIN MANAGEMENT AND USE OF PATIENT CONTROLLED ANALGESIA CAN LEAD TO HIGH QUALITY CARE AND HIGH PATIENT SATISFACTION IN THE PEDIATRIC EMERGENCY DEPARTMENT
MEASURES OF CLINICAL OUTCOMES IN VASO-OCCLUSIVE CRISIS OF SICKLE CELL DISEASE- GRADING THE LITERATURE
PULMONARY FUNCTION TESTING IN INFANTS WITH SICKLE CELL DISEASE
ABNORMAL RENAL TUBULAR HANDLING OF PHOSPHORUS IN SICKLE CELL DISEASE
PREVALENCE OF CYP2D6, CYP2C9 AND CYP2C19 ALLELIC VARIANTS IN A PEDIATRIC SICKLE CELL DISEASE PATIENT COHORT
LONGITUDINAL NATURAL HISTORY STUDY OF TRICUSPID REGURGITANT JET VELOCITY IN UNTREATED CHILDREN WITH SICKLE CELL DISEASE
Red Blood Cell Alloimmunization is Associated with Transfusion for Acute Sickle Cell disease-Related Complications
EVALUATION OF PURIFIED POLOXAMER 188 IN CHILDREN (EPIC) - KEY DESIGN CONSIDERATIONS
UNHEALTHY ALCOHOL USE AMONG PERSONS WITH SICKLE CELL DISEASE: PREVALENCE AND ASSOCIATION WITH CLINICAL OUTCOMES
PERCEIVED STIGMA AND EMERGENCY DEPARTMENT VISITS FOR SICKLE CELL DISEASE PAIN
AN INNOVATIVE APPROACH TO ENHANCING THE TRANSITION TO ADULT CARE IN SICKLE CELL DISEASE
Among Emergency Physicians, Use of the Term Sickler is Associated with Negative Attitudes Towards People with Sickle Cell Disease
PATIENTS WITH SICKLE CELL DISEASE REPORT POORER COMMUNICATION THAN NATIONAL ESTIMATES OF AFRICAN-AMERICANS' EXPERIENCES
POPULATION-BASED SURVEILLANCE FOR SICKLE CELL DISEASE: PAST, PRESENT, FUTURE
IN VITRO HUMAN AND PRECLINICAL ANIMAL STUDIES OF ADENOSINE-BASED THERAPIES IN SICKLE CELL DISEASE
Prasugrel in Children with Sickle Cell Disease: Pharmacokinetic and Pharmacodynamic Characteristics from an Open-Label, Adaptive-Design, Dose-Ranging Study
DISEASE-SPECIFIC KNOWLEDGE VS. FUNCTIONAL HEALTH LITERACY AMONG CAREGIVERS OF CHILDREN WITH SICKLE CELL: IS THERE A DIFFERENCE?
EMERGENCY PROVIDER ATTITUDES TOWARDS SICKLE CELL PATIENTS
URINE SCREENING FOR BIOMARKERS OF ACUTE AND CHRONIC KIDNEY INJURY IN CHILDREN AND ADULTS WITH SICKLE CELL ANEMIA WITH AND WITHOUT ALBUMINURIA
HYDROXYUREA DECISION-MAKING DETERMINANTS IN CHILDREN AND ADOLESCENTS WITH SICKLE CELL DISEASE
DISTANCE LEARNING-TEACHING PROCESS AMONG PRIMARY HEALTH CARE PROFESSIONALS IN THE STATE OF MINAS GERAIS, BRAZIL
PERCEPTIONS OF ADOLESCENTS AND YOUNG ADULTS REGARDING SCHOOL AND ENVIRONMENTAL ISSUES RELATED TO SICKLE CELL DISEASE
Patient Perceptions of Treatment Options for Sickle Cell Disease: Transplant, Hydroxyurea & Gene Therapy
UTILIZATION OF SOCIAL MEDIAS AND ITS IMPACT ON PATIENT AND PROVIDER SICKLE CELL EDUCATION
Primary Care Providers Comfort Levels in Caring for Patients with Sickle Cell Disease
TRAINING PATIENT NAVIGATORS FOR RECRUITING PATIENTS TO SICKLE CELL DISEASE SPECIALTY CARE: THE SHIP HU STUDY
Hemoglobin in Sickle Cell Anemia Is Positively Correlated with 25-hydroxyvitamin D, the Clinical Indicator of Vitamin D Status
ALPHA THALASSEMIA AND TNF-A G308A POLYMORPHISM INFLUENCES THE RISK OF STROKE IN CHILDREN WITH SICKLE CELL ANEMIA
7TESIA BRAIN MRI PILOT/FEASIBILITY STUDY OF COGNITIVE IMPAIRMENT IN ADULT PATIENTS WITH HBSS DISEASE
NOVEL APPROACH TO DESCRIBING PAIN IMPACT ON FUNCTION OF SICKLE CELL YOUTH HOSPITALIZED FOR VASOOCCLUSIVE PAIN
POPULATION-BASED ANALYSIS OF HIGH HOSPITAL UTILIZATION (HHU) AMONG CHILDREN AND ADOLESCENTS WITH SICKLE CELL DISEASE (SCD)
HEMATOPOIETIC STEM CELL TRANSPLANTATION FOR SICKLE CELL DISEASE IN AN EIGHT-YEAR-OLD GIRL WITH SIGNIFICANT PSYCHOSOCIAL RISK FACTORS: AN ETHICAL CASE STUDY
PREVALENCE OF THE BETA-S GENE AMONG SCHEDULED CASTES, SCHEDULED TRIBES AND OTHER BACKWARD CLASSES IN CENTRAL INDIA
TRAINING PROVIDERS ON ISSUES OF RACE AND RACISM TO IMPROVE HEALTH CARE EQUITY
VIRTUAL MENTOR PROGRAM FOR YOUNG ADULTS WITH SICKLE CELL DISEASE TRANSITIONING FROM PEDIATRIC TO ADULT CARE
FURTHER EVIDENCE FOR VALIDATION OF THE ADOLESCENT PEDIATRIC PAIN TOOL IN YOUTH WITH SICKLE CELL HOSPITALIZED FOR VASOOCCLUSIVE PAIN
THE PSYCHOSOCIAL FUNCTIONING AND ACADEMIC ACHIEVEMENT IN SIBLINGS WITH AND WITHOUT SICKLE CELL DISEASE
DEVELOPMENT AND PRELIMINARY EVALUATION OF THE ASSESSMENT OF OPIOID TAKING BEHAVIORS AND ADHERENCE SCALE (AOTBA) IN PATIENTS WITH SICKLE CELL DISEASE
CLINICAL PRESENTATION OF SICKLE CELL DISEASE FROM A SINGLE CENTER IN CENTRAL INDIA: A PROSPECTIVE ANALYSIS
Depressive Symptoms and Disease Management Self Efficacy, Not Catastrophizing, Predict Pain Interference Independent of Pain Severity in Sickle Cell Disease: Results from the baseline IMPORT study.
IMPROVING EMERGENCY DEPARTMENT CARE FOR CHILDREN WITH SICKLE CELL DISEASE
SOCIAL BEHAVIORAL NEEDS OF PATIENTS WITH SICKLE CELL DISEASE
A REVIEW OF VITAMIN D DEFICIENCY, TREATMENT AND PATIENT KNOWLEDGE AMONG SICKLE DISEASE PATIENTS AND PARENTS
SICKLE CELL CONNECTS WITH THE CHRONIC PAIN SERVICE: A COLLABORATIVE CLINIC A QUALITY IMPROVEMENT PROJECT
NUTRITIONAL IMPACT OF SICKLE CELL ANEMIA: OBESITY CAN ALSO BE A PROBLEM IN SICKLE CELL ANEMIA
APPLICATION OF CLINICAL MICROSYSTEMS TO IMPROVE THE OUTPATIENT CARE OF PATIENTS WITH SICKLE CELL DISEASE (SCD)
PERCEIVED RACISM AND STIGMA AMONG ADOLESCENTS WITH SICKLE CELL DISEASE
VITAMIN D DEFICIENCY IN AN ADULT POPULATION WITH SICKLE CELL DISEASE
Jonathan Douglas Santoro, MS,
SPINAL INFARCTION IN SICKLE CELL DISEASE, A RARE AND UNEXPLAINED COMPLICATION
READINESS CHECKLIST: PREPARING FOR TRANSFER OF MEDICAL CARE
PROGRAM FOR CONTINUING LEARNING ON SICKLE CELL DISEASE FOR PRIMARY HEALTH CARE PROFESSIONALS IN THE STATE OF MINAS GERAIS, BRAZIL
PATIENT CENTERED APPROACH TO DESIGNING SICKLE CELL TRANSITION EDUCATION
AT THE CROSSROADS OF INFLAMMATION AND COAGULATION: HSP90 INHIBITION IN SICKLE CELL DISEASE
NATIONAL ESTIMATES OF SICKLE CELL DISEASE WITH PEDIATRIC STROKE AMONG AFRICAN-AMERICANS—UNITED STATES, 1997-2009
AN ASSESSMENT OF DISEASE KNOWLEDGE DIFFERENCESBETWEEN ADOLESCENTS WITH SICKLE CELL DISEASE AND THEIR CAREGIVERS AND ITS CORRELATION TO QUALITY OF LIFE
DEVELOPMENT AND PRELIMINARY VALIDATION OF A MULTI-DIMENSIONAL ELECTRONIC PAIN DIARY FOR CHILDREN WITH SICKLE CELL DISEASE
ASPEN SYNDROME REVISITED (ASSOCIATION OF SICKLE CELL DISEASE, PRIAPISM, EXCHANGE TRANSFUSION AND NEUROLOGICAL EVENTS)
SPONTANEOUS EPIDURAL HEMATOMA COMPLICATING SICKLE CELL ANEMIA
Beta-S gene prevalence among socio-economically disadvantaged ethnic groups in Central India
A NOVEL IMAGING MODALITY FOR MANAGEMENT OF SICKLE CELL DISEASE PATIENTS WITH MOYAMOYA SYNDROME
MANAGEMENT AND MEASUREMENT OF PRURITUS IN SICKLE CELL DISEASE PATIENTS (SCD)
UTILIZING REFLECTIVE WRITING TO IMPROVE MEDICAL EDUCATION AND CULTURAL COMPETENCE REGARDING THE CARE OF SICKLE CELL DISEASE
PROCESS OF DISSEMINATING KNOWLEDGE ON SICKLE CELL DISEASE TO PRIMARY HEALTH CARE PROFESSIONALS IN THE STATE OF MINAS GERAIS, BRAZIL
PILOT PROGRAM FOR ESCAPE: ELECTRONIC SICKLE CELL APPLICATION FOR PAIN EVALUATION FOR PATIENTS ENROLLED IN NKT 120-SCD1
PEER MENTORING FOR ADOLESCENTS AND YOUNG ADULTS WITH SICKLE CELL DISEASE
ERYTHROPOIETIN LEVEL IN SICKLE CELL DISEASE PATIENTS NOT IN CRISIS
EFFECTS OF DENTAL CARE ON ACUTE CARE UTILIZATION FOR INDIVIDUALS WITH SICKLE CELL DISEASE
LONGITUDINAL ANALYSIS OF EMOTIONAL AND BEHAVIORAL PROBLEMS IN YOUTH WITH SICKLE CELL DISEASE USING THE PROBLEM SYMPTOM CHECKLIST-17
DEVELOPMENT OF A MULTI-DISCIPLINARY INPATIENT PROGRAM FOR CHILDREN WITH SICKLE CELL DISEASE ADMITTED FOR VASO-OCCULUSIVE CRISIS
RAPIDLY FATAL PNEUMOCOCCAL SEPSIS IN A YOUNG ADULT WITH SICKLE CELL DISEASE
EFFECT OF VITAMIN D AND CALCIUM SUPPLEMENTATION ON BONE MINERAL DENSITY IT PEDIATRIC SICKLE CELL DISEASE PATIENTS
MOBILE DIRECTLY OBSERVED THERAPY: MONITORING AND IMPROVING HYDROXYUREA ADHERENCE IN PEDIATRIC SICKLE CELL PATIENTS
IMPROVING HEALTH LITERACY AMONG THE SOCIO-ECONOMICALLY DISADVANTAGED SCHEDULED TRIBES FOR SICKLE CELL AND OTHER DISEASES IN SOUTHERN INDIA
ETHICAL AND CLINICAL CONSIDERATIONS IN AN ADOLESCENT JEHOVAH'S WITNESS WITH SICKLE CELL ANEMIA
PERCEPTIONS OF HOSPITAL READMISSION IN PATIENTS DIAGNOSED WITH SICKLE CELL DISEASE
EFFECT OF WEATHER ON FREQUENCY OF VASO-OCCLUSIVE CRISIS IN CHILDREN WITH SICKLE-CELL DISEASE IN OUR POPULATION
EFFECTIVENESS OF EDUCATIONAL INTERVENTION IN IMPROVING KNOWLEDGE AND PERCEPTION AMONG HEALTHCARE PROVIDERS AT A COMMUNITY-BASED HOSPITAL
SAFETY AND LONG-TERM EFFECTS OF SPLENECTOMY AT THE AGE OF TWO FOR ACUTE SPLENIC SEQUESTRATION IN SICKLE CELL DISEASE: A RETROSPECTIVE REVIEW
HYDROXYUREA THERAPY IN SICKLE CELL DISEASE: AN ALTERNATIVE APPROACH TO PREOPERATIVE RED CELL TRANSFUSION?
EPIDEMIOLOGY AND VARIABLES DEFINING SEVERITY OF SICKLE CELL DISEASE: A SINGLE INSTITUTION EXPERIENCE
ASYMMETRICAL IMPACT OF SICKLE CELL ANEMIA ON CARDIAC CAVITIES
(A) THE LUNGS AND BRAIN IN SICKLE CELL DISEASE: ORGANS AT RISK OF INJURY DUE TO PERTURBATIONS IN THE HEME DEGRADATION PATHWAY
(A) NEWBORN SCREENING FOR SICKLE CELL DISEASE AND OTHER HEMOGLOBINOPATHIES IN IBADAN, NIGERIA
IN VITRO HUMAN AND PRECLINICAL ANIMAL STUDIES OF ADENOSINE-BASED THERAPIES IN SICKLE CELL DISEASE
FINAL RESULTS OF A RANDOMIZED, OPEN-LABEL, MULTICENTER, 26-WEEK DOSE ESCALATION STUDY OF HQK-1001 (2,2-DIMETHYLBUTYRATE, SODIUM SALT) IN SICKLE CELL DISEASE (SCD)
STUDIES OF CLINICAL STAGE HBF INDUCERS IN SUB-GENOTYPED SICKLE ERYTHROID PROGENITORS AND PRIMATES
DISCOVERY AND HIGH-THROUGHPUT SCREENING AT THE UNIVERSITY OF KANSAS
ASE 1, FIRST-IN-MAN, DOSE-RESPONSE STUDY OF AES-103 (5-HMF), AN ANTI-SICKLING, ALLOSTERIC MODIFIER OF HEMOGLOBIN OXYGEN AFFINITY IN HEALTHY NORMAL VOLUNTEERS
lot Study of Eptifibatide for Treatment of Acute Pain Episodes in Sickle Cell Disease
LOST IN TRANSLATION: COMPLEX INTERACTIONS IN SICKLE CELL DISEASEMAY INTERFERE WITH TARGETED THERAPEUTICS
EVALUATION OF PURIFIED POLOXAMER 188 IN CHILDREN (EPIC) - KEY DESIGN CONSIDERATIONS
A PHASE I SINGLE ASCENDING DOSE STUDY OF NKTT120 IN STABLE ADULT SCD PATIENTS
IS THERE A ROLE FOR A RHEOLOGIC AGENT IN TRANSFUSION?
A PHASE 3, DOUBLE-BLIND, RANDOMIZED, EFFICACY AND SAFETY COMPARISON OF PRASUGREL AND PLACEBO IN PEDIATRIC PATIENTS WITH SICKLE CELL DISEASE