721 results on '"Manwani, Deepa"'
Search Results
2. Expert consensus on the management of infusion-related reactions (IRRs) in patients with sickle cell disease (SCD) receiving crizanlizumab: a RAND/UCLA modified Delphi panel
3. Pediatric brain aneurysms: a review of 1458 brain MR angiograms
4. COVID-19 mRNA vaccination responses in individuals with sickle cell disease: an ASH RC Sickle Cell Research Network Study
5. Biopsychosocial Factors Associated With Pain and Pain-Related Outcomes in Adults and Children With Sickle Cell Disease: A Multivariable Analysis of the GRNDaD Multicenter Registry
6. Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects
7. Macrophage metabolic rewiring improves heme-suppressed efferocytosis and tissue damage in sickle cell disease
8. Venous thromboembolism prophylaxis practices for patients with sickle cell disease prior to and during the COVID-19 pandemic
9. Elucidating parasite and host-cell factors enabling Babesia infection in sickle red cells under hypoxic/hyperoxic conditions
10. A microfluidic device for assessment of E-selectin-mediated neutrophil recruitment to inflamed endothelium and prediction of therapeutic response in sickle cell disease
11. Pharmacokinetics, pharmacodynamics, safety, and efficacy of crizanlizumab in patients with sickle cell disease
12. Using the “Coach Approach”: A Novel Peer Mentorship Program for Pediatric Faculty
13. Transition Navigator Intervention Improves Transition Readiness to Adult Care for Youth With Sickle Cell Disease
14. Hemolysis dictates monocyte differentiation via two distinct pathways in sickle cell disease vaso-occlusion
15. Global geographic differences in healthcare utilization for sickle cell disease pain crises in the CASiRe cohort
16. Age of first pain crisis and associated complications in the CASiRe international sickle cell disease cohort
17. Prevent Acute Chest Syndrome checklist (PACScheck): A quality improvement initiative to reduce acute chest syndrome.
18. Hemolysis inhibits humoral B-cell responses and modulates alloimmunization risk in patients with sickle cell disease
19. Clinical predictors of poor outcomes in patients with sickle cell disease and COVID-19 infection
20. Atypical hemolytic uremic syndrome during induction chemotherapy in neuroblastoma, a rare phenomenon or common congenital predisposition?
21. Assessing multilevel barriers to hydroxyurea adherence in youth with sickle cell disease using pharmacy‐based refill records.
22. Draining Vein Thrombosis of Developmental Venous Anomaly in Sickle Cell Trait Patients: A Case Report and a Literature Review.
23. Randomized phase 2 trial of Intravenous Gamma Globulin (IVIG) for the treatment of acute vaso-occlusive crisis in patients with sickle cell disease: Lessons learned from the midpoint analysis
24. 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
25. An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research
26. A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysis
27. Pathobiology of Sickle Cell Disease Vaso-occlusion and Targeted Therapies
28. Patrolling monocytes scavenge endothelial-adherent sickle RBCs: a novel mechanism of inhibition of vaso-occlusion in SCD
29. Evaluating thromboprophylaxis in the sickle cell disease population: Navigating the evidence gap.
30. Pain Frequency and Health Care Utilization Patterns in Women with Sickle Cell Disease Experiencing Menstruation-Associated Pain Crises
31. The Newborn with Hematologic Abnormalities
32. HABIT, a Randomized Feasibility Trial to Increase Hydroxyurea Adherence, Suggests Improved Health-Related Quality of Life in Youths with Sickle Cell Disease
33. HO-1hi patrolling monocytes protect against vaso-occlusion in sickle cell disease
34. Association of silent infarcts in sickle cell anemia with decreased annexin A5 resistance
35. Liver Stiffness Measurement by Vibration Controlled Transient Elastography Does Not Correlate to Hepatic Iron Overload in Children With Sickle Cell Disease
36. Biopsychosocial Factors Associated With Pain and Pain-Related Outcomes in Adults and Children With Sickle Cell Disease: A Multivariable Analysis of the GRNDaD Multicenter Registry
37. PB2516: ACTIGRAPHY IMPROVEMENT WITH VOXELOTOR (ACTIVE) STUDY: IMPACT OF VOXELOTOR ON PHYSICAL ACTIVITY, FATIGUE, AND SLEEP QUALITY
38. Long‐term clinical outcomes and healthcare utilization of sickle cell disease patients with COVID‐19: A 2.5‐year follow‐up study
39. An age dependent response to hydroxyurea in pediatric sickle cell anemia patients with alpha thalassemia trait
40. A Randomized Trial of Yoga for Children Hospitalized With Sickle Cell Vaso-Occlusive Crisis
41. List of Contributors
42. Coagulopathy in Sickle Cell Disease
43. Acute (Childhood) Immune Thrombocytopenia
44. Approach to the Pediatric Patient With a Bleeding Disorder
45. Neutrophils, platelets, and inflammatory pathways at the nexus of sickle cell disease pathophysiology
46. HABIT efficacy and sustainability trial, a multi-center randomized controlled trial to improve hydroxyurea adherence in youth with sickle cell disease: a study protocol
47. Associating a standardized reporting tool for chest radiographs with clinical complications in pediatric acute chest syndrome.
48. Dietary iron restriction protects against vaso-occlusion and organ damage in murine sickle cell disease
49. Serial assessment of laser Doppler flow during acute pain crises in sickle cell disease
50. Impact of magnetic resonance angiography parameters on stroke prevention therapy in pediatric patients with sickle cell anemia
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