37 results on '"Appiah‐Kubi, Abena"'
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2. Cardiac complications of sickle cell disease in pediatric patients: A case report and contemporary literature review
3. Assessing multilevel barriers to hydroxyurea adherence in youth with sickle cell disease using pharmacy‐based refill records.
4. Longitudinal analysis of cardiac abnormalities in pediatric patients with sickle cell anemia and effect of hydroxyurea therapy
5. Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment (HABIT) efficacy trial: Community health worker support may increase hydroxyurea adherence of youth with sickle cell disease
6. Documented Viral Illness at the Time of Splenic Sequestration Does Not Affect the Odds of Recurrence in Children With Sickle Cell Disease
7. Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia
8. Pomalidomide reverses γ-globin silencing through the transcriptional reprogramming of adult hematopoietic progenitors
9. Individualized, PK-Guided Dosing of Hydroxyurea Is Not Associated with Increased Hematologic Toxicity Compared to Weight-Based Initial Dosing: Interim Results from the Hops Trial
10. Assessing Multi-Level Barriers to Medication Adherence in Youth with Sickle Cell Disease Using Pharmacy-Based Prescription Refill Data
11. Mental health assessment of youth with sickle cell disease and their primary caregivers during the COVID‐19 pandemic
12. Mental Health Assessment of Youth with Sickle Cell Disease and Their Primary Caregivers During the COVID-19 Pandemic
13. Multisystem inflammatory syndrome in children (MIS‐C) and the prothrombotic state: Coagulation profiles and rotational thromboelastometry in a MIS‐C cohort
14. Effect of COVID‐19 on anakinra‐induced remission in homozygous STX11 hemophagocytosis lymphohistiocytosis
15. Safety and benefits of automated red cell depletion‐exchange compared to standard exchange in patients with sickle cell disease undergoing chronic transfusion
16. NT‐proBNP levels and cardiopulmonary function in children with sickle cell disease
17. Mental Health Assessment of Youth with Sickle Cell Disease and Their Primary Caretakers: Baseline Depression and COVID-19 Pandemic-Associated Psychosocial Stress in a Multi-Site Study
18. Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia
19. Are children with SARS‐CoV‐2 infection at high risk for thrombosis? Viscoelastic testing and coagulation profiles in a case series of pediatric patients
20. The long road to the cure of sickle cell anemia: Reflections on race and medicine in America
21. Varying presentations and favourable outcomes of COVID‐19 infection in children and young adults with sickle cell disease: an additional case series with comparisons to published cases
22. A pilot study to screen for poor academic performance in children with sickle cell disease in the outpatient setting
23. Benefit and Safety of Isovolemic Hemodilution Prior to Red Cell Exchange in Chronically Transfused Sickle Cell Patients
24. Management of vaso‐occlusive episodes in the day hospital decreases admissions in children with sickle cell disease
25. LONGITUDINAL ANALYSIS OF ECHOCARDIOGRAPHIC ABNORMALITIES IN CHILDREN WITH SICKLE CELL DISEASE RECEIVING HYDROXYUREA
26. NT‐proBNP levels and cardiopulmonary function in children with sickle cell disease.
27. Safety and benefits of automated red cell depletion‐exchange compared to standard exchange in patients with sickle cell disease undergoing chronic transfusion.
28. Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation
29. Transfusion-transmitted babesiosis leading to severe hemolysis in two patients with sickle cell anemia
30. Habit Efficacy Trial: A Multi-Site Randomized Controlled Trial of Community Health Worker Support to Increase Hydroxyurea Adherence of Youth with Sickle Cell Disease
31. Pomalidomide Transcriptionally Reprograms Adult Erythroid Progenitors Independently of Ikaros Proteasomal Degradation
32. Comparison of Impulse Oscillometry with Spirometry to Assess Lung Function in Children with Sickle Cell Disease (SCD)
33. Pomalidomide Modulates Transcription Networks Regulating Human Erythropoiesis and Globin Switching: Implications for Treatment of Hemoglobinopathies
34. Pomalidomide Augments Fetal Hemoglobin Production In Primary Erythroid Cells By a Novel Mechanism Modulating BCL11A But Not KLF-1
35. Transfusion-transmitted babesiosis leading to severe hemolysis in two patients with sickle cell anemia.
36. The long road to the cure of sickle cell anemia: Reflections on race and medicine in America
37. What's Your Diagnosis?®.
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