168 results on '"DeBaun, Michael"'
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2. Digital cognitive behavioral therapy vs education for pain in adults with sickle cell disease
3. Incremental eligibility criteria for the BMT CTN 1507 haploidentical trial for children with sickle cell disease
4. An international learning collaborative phase 2 trial for haploidentical bone marrow transplant in sickle cell disease
5. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels
6. Cerebral hemodynamic changes after haploidentical hematopoietic stem cell transplant in adults with sickle cell disease
7. A multilevel mHealth intervention boosts adherence to hydroxyurea in individuals with sickle cell disease
8. Risk factors in underweight older children with sickle cell anemia: a comparison of low- to high-income countries
9. Feasibility trial for the management of severe acute malnutrition in older children with sickle cell anemia in Nigeria
10. A feasibility randomized controlled trial of an mHealth app vs booklets for patient-facing guidelines in adults with SCD
11. Creating an automated contemporaneous cohort in sickle cell anemia to predict survival after disease-modifying therapy
12. Most adults with severe HbSC disease are not treated with hydroxyurea
13. Underweight children older than 5 years with sickle cell anemia are at risk for early mortality in a low-resource setting
14. Hydroxyurea for secondary stroke prevention in children with sickle cell anemia in Nigeria: a randomized controlled trial
15. Incidence and predictors of priapism events in sickle cell anemia: a diary-based analysis
16. Economic evaluation of regular transfusions for cerebral infarct recurrence in the Silent Cerebral Infarct Transfusion Trial
17. Capacity Building for Primary Stroke Prevention Teams in Children Living With Sickle Cell Anemia in Africa
18. A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease
19. Intracranial and Extracranial Vascular Stenosis as Risk Factors for Stroke in Sickle Cell Disease
20. Men with sickle cell disease experience greater sexual dysfunction when compared with men without sickle cell disease
21. Is allogeneic transplantation for sickle cell disease still relevant in the era of gene therapy?
22. Phase 2 trial of montelukast for prevention of pain in sickle cell disease
23. End points for sickle cell disease clinical trials: patient-reported outcomes, pain, and the brain
24. 2019 sickle cell disease guidelines by the American Society of Hematology: methodology, challenges, and innovations
25. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma
26. Bridging the childhood epilepsy treatment gap in northern Nigeria (BRIDGE): Rationale and design of pre-clinical trial studies
27. Haploidentical Bone Marrow Transplantation with Post-Transplantation Cyclophosphamide Plus Thiotepa Improves Donor Engraftment in Patients with Sickle Cell Anemia: Results of an International Learning Collaborative
28. Stroke Recurrence in Nigerian Children With Sickle Cell Disease: Evidence for a Secondary Stroke Prevention Trial
29. Silent infarcts in sickle cell disease occur in the border zone region and are associated with low cerebral blood flow
30. Key Components of Pain Management for Children and Adults with Sickle Cell Disease
31. The Epidemiology and Management of Lung Diseases in Sickle Cell Disease: Lessons Learned from Acute and Chronic Lung Disease in Cystic Fibrosis
32. Defining Undernutrition Risk Factors in Young Children With Sickle Cell Disease in Northern Nigeria
33. Primum non nocere: the case against transplant for children with sickle cell anemia without progressive end-organ disease
34. Exhaled nitric oxide: Not associated with asthma, symptoms, or spirometry in children with sickle cell anemia
35. Improved Guideline Adherence With Integrated Sickle Cell Disease and Asthma Care
36. Central nervous system complications and management in sickle cell disease
37. Low forced expiratory volume is associated with earlier death in sickle cell anemia
38. How I treat and manage strokes in sickle cell disease
39. The use of FDA-approved medications for preventing vaso-occlusive events in sickle cell disease
40. Headache and Migraine in Children with Sickle Cell Disease Are Associated with Lower Hemoglobin and Higher Pain Event Rates But Not Silent Cerebral Infarction
41. Environmental Tobacco Smoke and Airway Obstruction in Children With Sickle Cell Anemia
42. Evaluation of hemoglobin S percent threshold to prevent severe pain events: a secondary analysis of the SIT trial
43. Sickle hemoglobin disturbs normal coupling among erythrocyte O2 content, glycolysis, and antioxidant capacity
44. Rationale and Design of a Randomized Controlled Double-Blind Internal Pilot Trial for Prevention of Recurrent Ischemic Priapism in Men with Sickle Cell Disease (PIN Trial)
45. Outcomes of Non-Myeloablative HLA-Haploidentical Bone Marrow Transplant with Thiotepa and Post-Transplant Cyclophosphamide in Children and Adults with Sickle Cell Disease, a Phase II Trial: Vanderbilt Global Haploidentical Transplant Learning Collaborative (VGC2)
46. Interim Analysis of a Phase 2 Trial to Assess the Efficacy and Safety of Crizanlizumab in Sickle Cell Disease Patients with Priapism (SPARTAN)
47. Progressive Silent Cerebral Infarcts Are Prevalent in Adults with Sickle Cell Anemia but Moderate-Severe Cognitive Abnormalities Are Independent of Preexisting Silent Cerebral Infarcts
48. Silent Cerebral Infarction during Immune TTP Remission - Prevalence, Predictors and Impact on Cognition
49. Sexual violence as a precipitator of chronic pain in young adults with sickle cell disease
50. Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease
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