Iron overload and stem cell transplant—and the beat goes on
Erythrocyte pyruvate kinase deficiency in an old-order Amish cohort: Longitudinal risk and disease management
Inflammation, TNFα and endothelial dysfunction link lenalidomide to venous thrombosis in chronic lymphocytic leukemia
Utility of positron emission tomography scans in mantle cell lymphoma
Stroke recurrence in children with sickle cell disease treated with hydroxyurea following first clinical stroke
Annual clinical updates in hematological malignancies: A continuing medical education series. Hodgkin lymphoma: 2011 update on diagnosis, risk-stratification, and management
Thrombotic microangiopathy complicating pegylated interferon treatment of hepatitis C infection
Safety and efficacy of rapidly administered (one hour) one gram of low molecular weight iron dextran (INFeD) for the treatment of iron deficient anemia
When children with sickle-cell disease become adults: Lack of outpatient care leads to increased use of the emergency department
Possible new LNK mutations in myeloproliferative neoplasms
Concomitant lupus anticoagulant and monoclonal IgMκ antibody in a patient with bleeding tendency: A case report and literature review
Treatment of vitamin D deficiency in transfusion-dependent thalassemia
Cyclophosphamide and prednisone induction followed by cyclophosphamide mobilization effectively decreases the incidence of engraftment syndrome in patients with POEMS syndrome who undergo stem cell transplantation
Circulating cytokine levels, Epstein-Barr viremia, and risk of acquired immunodeficiency syndrome-related non-Hodgkin lymphoma
Peritransplant palifermin use and lymphocyte recovery after T-cell replete, matched related allogeneic hematopoietic cell transplantation
Lenalidomide-associated pneumonitis in patients with plasma cell dyscrasias
Managing cardiac amyloidosis: Auto or allotransplant?
Successful treatment with recombinant soluble thrombomodulin of two cases of sinusoidal obstructive syndrome/hepatic veno-occlusive disease after bone marrow transplantation
Hydroxyurea use in patients with sickle cell disease in a Medicaid population
Basophils and plasmacytoid dendritic cells are potential sources for error in flow cytometric monitoring of patients receiving anti-CD22 therapies. AKA not all anti-CD22 antibodies are created equal
Rapid response of plasmacytomas to lenalidomide plus low-dose dexamethasone therapy in a patient with relapsed multiple myeloma
Scleromyxedema and dermato–neuro syndrome in a patient with multiple myeloma effectively treated with dexamethasone and bortezomib
Iron overload and iron chelation therapy in patients with myelodysplastic syndrome treated by allogeneic stem-cell transplantation: Report from the working conference on iron chelation of the Gruppo Italiano Trapianto di Midollo Osseo
Erratum: Costs and length of stay for patients with and without sickle cell disease after hysterectomy, appendectomy, or knee replacement
Erratum: Outcomes of inpatients with and without sickle cell disease after high-volume surgical procedures
Diagnostic Challenge Presented by “Hb F only” Pattern in Newborn Screening for Hemoglobinopathies: Approach to Accurate Diagnosis
Detrimental Effects of A2B Adenosine Receptor-Mediated 2,3-Diphosphoglycerate Induction in Erythrocyte Sickling and Novel Mechanism-Based Therapies
Genetic Signatures of Sickle Cell Disease Severity
TR2/4 Overexpression Significantly Induces Fetal Hemoglobin Production within Humanized Sickle Cell Disease Mice
Non-myeloablative Hematopoietic Stem Cell Transplant Fails to Correct Renal Dysfunction in Aged Sickle Cell Mice
Fetal Hemoglobin in Sickle Cell Anemia: The ‘High’ HbF Phenotype
Oral Glutamine Supplementation Improves Global Arginine Bioavailability in Patients With Sickle Cell Disease and Doppler-Defined Pulmonary Hypertension: Preliminary Pharmacokinetics Results
Vitamin D Deficiency in Pediatric Patients With Sickle Cell Disease Correlates with Age and With Baseline Hemoglobin but Not With Disease Severity
Enhancing Enrollment of Sickle Cell Patients in Clinical Research Studies
Chronically Transfused Pediatric Sickle Cell Patients Are Protected From Cardiac Iron Overload
Pain Intensity during the Initial Experience with the IMPROVE Trial-a Phase III Analgesic Trial for Hospitalized Sickle Cell Painful Episodes
Ten-year Experience With a Dual-lumen Port For Chronic Erythrocytapheresis (cRBCX) for Individuals With Sickle Cell Disease: a Single Center Experience
Retinopathy in Patients With Sickle Cell Disease.
Lower Absolute Neutrophil Counts (ANC) Are Associated With Fewer Painful Crises in Individuals With Sickle Cell Disease (SCD) on Hydroxyurea (HU): Results From Walk-PHaSST Screening Database.
Niacin Therapy and Endothelial Function in Sickle Cell Disease
Clinical Trial Implementation and Planning: Lessons Learned from the Early Termination of a Randomized Trial for Pain Management in Sickle Cell Disease
Longitudinal Study of Echocardiographically-Derived Tricuspid Regurgitant Jet Velocity in Sickle Cell Disease
Systemic Blood Pressure is Associated with Anemia and Placenta Growth Factor in Sickle Cell Anemia
Relationship of Liver Iron Concentration With Hepatic and Cardiac R2* in Adults With Sickle Cell Anemia.
Process and Outcomes of Vaso-occlusive Crisis Treatment in an SCD Infusion Center: Implications for Quality Improvement Efforts
Initial Evaluation of the Pediatric PROMIS Health Domains in Children and Adolescents with Sickle Cell Disease (SCD)
Markers of Severe Vaso-occlusive Painful Episodes in Children and Adolescents With Sickle Cell Anemia
Pain in Infants and Young Children with Sickle Cell Disease - A Prospective Longitudinal Analysis
Opioid PCA Usage during the Initial Experience with the IMPROVE Trial-a Phase III Analgesic Trial for Hospitalized Sickle Cell Painful Episodes
Refining the Predictive Value of Secretory Phospholipase A2 for Acute Chest Syndrome in Adults and Children with Sickle Cell Disease Hospitalized for Pain
Severe Cardiac Iron Accumulation Occurs and May Be Common in Older, Hypertransfused Sickle Cell Patients
Oocyte Cryopreservation as a Means for Fertility Preservation Prior to Hematopoietic Stem Cell Transplantation: First Report in a Patient with Sickle Cell Disease
Randomized Double Blind Study Evaluating Response to High Dose Vitamin D Therapy in Pediatric Sickle Cell Disease
Sickle Cell Day Hospital at Memorial Regional Hospital - A Solution That Works
Pulmonary Hypertension and Proteinuria in Children with Sickle Cell Disease
Wounding Stimulates Long-Term Alterations in Vasculature, Nerve Fibers and Neuropeptides in the Skin of Mice Expressing Sickle Hemoglobin
Assessing the Nutrition Status of women with sickle cell disease enrolled in the WIC program at the Juanita Mann Community Clinic in Liberty City, Florida Using a Dietary Intake Questionnaire: A Needs Assessment
Project I.N.F.A.N.T CareCard Program: A Tool to Improve Access to Quality Care For Children and Adults living with Sickle Cell Disease
A Community Based Educational Support Program for Children with Sickle Cell Disease Improves School Attendance and Educational Performance
Adolescent and Young Adult Transition Support Program: A Bridge to Effective Transition to Adult Care.
Does Tonsillectomy Incidentally Decrease the Frequency of Nocturnal Enuresis in Children and Adolescents with Sickle Cell Disease?
Preferences For Genetic Counseling and Educational Materials for African Immigrant Families With A Child Diagnosed With Sickle Cell Disease
Visual-Motor Integration Difficulties in Sickle Cell Disease
Sickle Cell Trait Counseling for Student-Athletes
Design and Creation of a Web-based Educational Intervention for Sickle Cell Disease Adolescent Transition
Survey Review of a Family Education Symposium: Transplantation to Cure Sickle Cell Disease
Genetic Counseling for Everyone: Increasing Availability in a Sickle Cell Network
The Baby Sickle Training and Education Program (BabySTEP®: Utilization and Impact on Parental Knowledge
A New Approach to Sickle Cell Family Education on Bone Marrow Transplantation - Panel Discussion Conference
Pediatric Comprehensive Sickle Cell Program Certification as a Medical Home: The Pittsburgh Experience
Perceived Barriers and Benefits to Participation in Medical and Psychosocial Clinical Trials for Youth with Sickle Cell Disease and Youth with Asthma and their Caregivers
Improving Access to Pulmonary Care for Children with Sickle Cell Disease
Illness Representations Among Adolescents with Different Chronic Illnesses
Incidental Finding: Adult Sickle Cell Readmissions are Reduced with the Implementation of the PAST (Proactive and Aggressive Sickle Cell Disease Treatment) Model
Barriers to Clinical Trial Participation of African American and Black Youth with Sickle Cell Disease and Their Parents
The Development of the PedsQL™ Sickle Cell Disease Module Items: Qualitative Methods
Educational and Vocational Needs of Adolescents with Sickle Cell Disease During the Transition to Adult Care
The Incidence and Treatment of Obstructive Sleep Apnea among Children and Adolescents with Sickle Cell Disease
Use of Life Course Model to Prepare Children with Sickle Cell Disease for Adult Life
A Retrospective Review of Medication Administration Records Comparing Ondansetron with Diphenhydramine in the Treatment of Pruritus in Hospitalized Sickle Cell Patients: Outcomes Data
Development of a Measure to Assess Barriers to Care in Sickle Cell Disease
Patient Navigation: Effectiveness of a Model for Sickle Cell Disease
Family Sharing of Disease Management in Pediatric Sickle Cell Disease
Cocaine Use in Patients with Sickle Cell Disease and Chronic Opioid Treatment
Evaluation of a Multidisciplinary Transition Program
A Provider-Based Self-Management Intervention to Improve Exjade® Adherence in Pediatric SCD
Sleep Problems in Pediatric Sickle Cell Disease and the Impact on Cognition
Sickle Cell Disease: Discussing Disparity
Application of Clinical Microsystems to Improve the Initial Pain Relief in Sickle Cell Disease (SCD) Patients Admitted with Acute Vaso-Occlusive Crisis
Cue Recognition and Response to Sickle Cell Pain
Preliminary Measurement of Stigma in a Sample of Young Adults with Sickle Cell Disease
Speed of Mental Processing in Pediatric Sickle Cell Disease
Crossing the Great Divide: A Conversation Between Ghana Young Adults With SCD and United States Practitioners
Nurse Initiated Evidence Based Acute Sickle Cell Pain Management in the Emergency Department
After the Transition: Adjustment of Pediatric Patients with Sickle Cell Disease to Adult Centered Care
Building a Community-Based Chronic Transfusion Program for Patients with Sickle Cell Disease: An ANSCAPE Program
Community Based Comprehensive Care for Sickle Cell Disease for a Remote Tribal Population in Nilgiri Hills, Southern India
Health-Related Quality of Life Measures used in Children and Adolescents with Sickle Cell Disease: An Integrative Literature Review
Newborn screening for Sickle Cell Disease in a Tribal Area of South Gujarat, India
Community Based Comprehensive Program to Enhance Follow-up of Newborn Screening for Sickle cell Disease in the Western Pennsylvania Sickle Cell Network
How is Patient Socioeconomic Status Related to Health Care Utilization?
Gujarat State Sickle Cell Program: a Public-Private Partnership in Comprehensive Community Based Care Delivery
Acceptance of Prenatal Diagnosis of Sickle Cell Disease in a Tribal Population of Gujarat, India: A Preliminary Study at Valsad Raktdan Kendra
“Floor the Pain” A Novel Approach for Direct Hospital Admission and Multidisciplinary Team Management of Vasoocclusive Pain Crisis Management in patients with Sickle Cell Disease
Maternal Roles, Mental Health Problems and Sickle Cell Disease
Clinical Vignette - 18y Male With Sickle Cell Disease and Chronic Penile Erection
Clinical Vignette - Hepatosplenic γδ T-Cell Lymphoma In A Patient With Sickle Cell Disease
Clinical Vignette - Intimate Partner Violence in Sickle Cell Disease: Nurses Be Aware
Clinical Vignette - Is It OK To Send Children With Sickle Cell Disease Who Reside in Colorado to Camp at 6300 Feet?
Clinical Vignette - Liver Disease
Clinical Vignette - The Reluctant Response
Clinical Vignette - Liver Complication in a Young Patient with Hemoglobin SS Disease
Clinical Vignette - Ketamine for Severe Sickle Cell Painful Episodes in an Opioid Tolerant Patient
Clinical Vignette - When Is A Stroke Not A Stroke?
Clinical Vignette - Avascular Necrosis of the Femoral Head in a 7 year old with Sickle Cell Disease
Clinical Vignette - Management of an Adult Patient With Sickle Cell Disease, Chronic Pain and Depression
Support & Stress BOTH Affect Behavior Adjustment in Children with SCD.
Topical Application of Morphine Facilitates Wound Closure in S+S Antilles Mice which also Exhibit Age-related Sensitization to Cold.
Outcome of Iron Chelation Therapy
Sickle-Hereditary Persistence of Fetal Hemoglobin - An Enigma?