88 results on '"Debaun, Michael R."'
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2. Cerebral hemodynamic changes after haploidentical hematopoietic stem cell transplant in adults with sickle cell disease
3. Risk factors in underweight older children with sickle cell anemia: a comparison of low- to high-income countries
4. A feasibility randomized controlled trial of an mHealth app vs booklets for patient-facing guidelines in adults with SCD
5. Feasibility trial for the management of severe acute malnutrition in older children with sickle cell anemia in Nigeria
6. Creating an automated contemporaneous cohort in sickle cell anemia to predict survival after disease-modifying therapy
7. Most adults with severe HbSC disease are not treated with hydroxyurea
8. Underweight children older than 5 years with sickle cell anemia are at risk for early mortality in a low-resource setting
9. Hydroxyurea for secondary stroke prevention in children with sickle cell anemia in Nigeria: a randomized controlled trial
10. Incidence and predictors of priapism events in sickle cell anemia: a diary-based analysis
11. Economic evaluation of regular transfusions for cerebral infarct recurrence in the Silent Cerebral Infarct Transfusion Trial
12. Men with sickle cell disease experience greater sexual dysfunction when compared with men without sickle cell disease
13. End points for sickle cell disease clinical trials: patient-reported outcomes, pain, and the brain
14. 2019 sickle cell disease guidelines by the American Society of Hematology: methodology, challenges, and innovations
15. Bridging the childhood epilepsy treatment gap in northern Nigeria (BRIDGE): Rationale and design of pre-clinical trial studies
16. 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
17. Silent infarcts in sickle cell disease occur in the border zone region and are associated with low cerebral blood flow
18. Evaluation of hemoglobin S percent threshold to prevent severe pain events: a secondary analysis of the SIT trial
19. Exhaled nitric oxide: Not associated with asthma, symptoms, or spirometry in children with sickle cell anemia
20. Central nervous system complications and management in sickle cell disease
21. Low forced expiratory volume is associated with earlier death in sickle cell anemia
22. How I treat and manage strokes in sickle cell disease
23. The Use of FDA-Approved Medications for Preventing Vaso-Occlusive Events in Sickle Cell Disease
24. Silent Cerebral Infarction during Immune TTP Remission - Prevalence, Predictors and Impact on Cognition
25. 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)
26. 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)
27. Interim Analysis of a Phase 2 Trial to Assess the Efficacy and Safety of Crizanlizumab in Sickle Cell Disease Patients with Priapism (SPARTAN)
28. Progressive Silent Cerebral Infarcts Are Prevalent in Adults with Sickle Cell Anemia but Moderate-Severe Cognitive Abnormalities Are Independent of Preexisting Silent Cerebral Infarcts
29. Sexual violence as a precipitator of chronic pain in young adults with sickle cell disease
30. Sickle hemoglobin disturbs normal coupling among erythrocyte O2 content, glycolysis, and antioxidant capacity
31. Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease
32. Enuresis Associated with Sleep Disordered Breathing in Children with Sickle Cell Anemia
33. Sustainability of low maternal mortality in pregnant women with SCD in a low-resource setting
34. Annual decline in lung function in adults with sickle cell disease is similar to that observed in adults with cystic fibrosis
35. Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia
36. Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure
37. Airway Hyperresponsiveness in Children With Sickle Cell Anemia
38. Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease
39. Risk Factors for 30-Day Readmission in Adults with Sickle Cell Disease
40. Left ventricular hypertrophy and diastolic dysfunction in children with sickle cell disease are related to asleep and waking oxygen desaturation
41. Addition of H19 ‘Loss of Methylation Testing’ for Beckwith-Wiedemann Syndrome (BWS) Increases the Diagnostic Yield
42. Histopathology of experimentally induced asthma in a murine model of sickle cell disease
43. Enuresis Is a Common and Persistent Problem Among Children and Young Adults with Sickle Cell Anemia
44. Decreased median survival of adults with sickle cell disease after adjusting for left truncation bias: a pooled analysis
45. Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients
46. No Specific Factors Associated with Risk of Readmission for Rebound Pain in Children with Sickle Cell Disease and Asthma Treated with Systemic Corticosteroids
47. Reversible posterior leukoencephalopathy syndrome and silent cerebral infarcts are associated with severe acute chest syndrome in children with sickle cell disease
48. Longitudinal changes in brain magnetic resonance imaging findings in children with sickle cell disease
49. Feasibility of partial nephrectomy for Wilms' tumor in children with Beckwith-Wiedemann syndrome who have been screened with abdominal ultrasonography
50. Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia
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