382 results on '"DeBaun, Michael"'
Search Results
2. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels
3. Hydroxyurea for secondary stroke prevention in children with sickle cell anemia in Nigeria: a randomized controlled trial
4. Silent infarcts in sickle cell disease occur in the border zone region and are associated with low cerebral blood flow
5. Reduced Intensity Haploidentical Bone Marrow Transplantation in Adults with Severe Sickle Cell Disease: BMT CTN 1507
6. Central nervous system complications and management in sickle cell disease
7. Low forced expiratory volume is associated with earlier death in sickle cell anemia
8. How I treat and manage strokes in sickle cell disease
9. Interim Analysis of a Phase 2 Trial to Assess the Efficacy and Safety of Crizanlizumab in Sickle Cell Disease Patients with Priapism (SPARTAN)
10. Progressive Silent Cerebral Infarcts Are Prevalent in Adults with Sickle Cell Anemia but Moderate-Severe Cognitive Abnormalities Are Independent of Preexisting Silent Cerebral Infarcts
11. 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)
12. No Specific Factors Associated with Risk of Readmission for Rebound Pain in Children with Sickle Cell Disease and Asthma Treated with Systemic Corticosteroids
13. Silent Cerebral Infarction during Immune TTP Remission - Prevalence, Predictors and Impact on Cognition
14. 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)
15. Sickle hemoglobin disturbs normal coupling among erythrocyte O2 content, glycolysis, and antioxidant capacity
16. Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease
17. Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia
18. Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure
19. Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease
20. Left ventricular hypertrophy and diastolic dysfunction in children with sickle cell disease are related to asleep and waking oxygen desaturation
21. Leukemia after gene therapy for sickle cell disease: insertional mutagenesis, busulfan, both, or neither
22. In Africa, a High Proportion of Adults with HbSC Meet American Society of Hematology's Eligibility Criteria for Severe Sickle Cell Disease and Starting Hydroxyurea Therapy in a Clinical Trial Setting
23. Cerebral Blood Flow, Brain Volume, and Age Predicts Executive Function in Sickle Cell Anemia
24. Histopathology of experimentally induced asthma in a murine model of sickle cell disease
25. Initiating adjunct low-dose hydroxyurea therapy for stroke prevention in children with SCA during the COVID-19 pandemic
26. Primary Analysis of Spartan: A Phase 2 Trial to Assess the Efficacy and Safety of Crizanlizumab in Patients with Sickle Cell Disease Related Priapism
27. Randomized Controlled Double Blind Feasibility Trial of Tadalafil with Hydroxyurea Versus Hydroxyurea with Placebo for Secondary Prevention of Recurrent Priapism in Men with Sickle Cell Anemia: Pin Trial Final Results
28. The Optimal Threshold for Hemoglobin S Percent Level While Performing Regular Blood Transfusion Therapy to Prevent Severe Vaso-Occlusive Pain Events in Children with Sickle Cell Anemia: A Secondary Data Analysis of Participants in the SIT Trial
29. The Importance of Screening for Food Insecurity in Children with Sickle Cell Anemia: An Ancillary Study to the Severe Acute Malnutrition Feasibility Trial in Nigeria
30. Localization of Silent Cerebral Infarcts in Children with Sickle Cell Disease Impacts Structural Disconnection
31. A Working Definition of Acute Chest Syndrome without the Requirement of Chest X-Rays
32. In Phase 2 and Phase 3 Trials, Broadening the Definition of Acute Vaso-Occlusive Pain to Include at Least One Episode of Pain Requiring Nsaids, Opioids, or Both Treatments at Home within 30 Days of a Physician Visit
33. Characterization of Sickle Cell Disease Mortality in a National Electronic Health Record (EHR) System
34. Assessing Pain Severity in Sickle Cell Disease Using Animations and a Graphical Body Image
35. A Genotype Validated Bimodal Method for the Large-Scale Identification and Phenotyping of Persons with Sickle Cell Disease Using Electronic Health Record Data
36. A Randomized Clinical Trial Testing the Effect of Digital Behavioral Interventions on Pain and Mental Health Among Adults with Sickle Cell Disease
37. Asthma is associated with acute chest syndrome and pain in children with sickle cell anemia
38. Randomized Controlled Trial of Fixed Low-Vs Moderate-Dose Hydroxyurea for Primary Stroke Prevention in Sub-Saharan Africa: Final Results of the Spring Trial
39. Low- Versus Moderate-Dose Hydroxyurea for Secondary Stroke Prevention in Children with Sickle Cell Disease in Sub-Saharan Africa: Final Results of a Randomized Controlled Trial, Sprint Trial
40. Outcomes of Non-Myeloablative HLA-Haploidentical Bone Marrow Transplant with Thiotepa and Post-Transplant Cyclophosphamide in Children and Adults with Severe Sickle Cell Disease, a Phase II Trial: Vanderbilt Global Haploidentical Transplant Learning Collaborative (VGC2)
41. Decreased median survival of adults with sickle cell disease after adjusting for left truncation bias: a pooled analysis
42. Reversible posterior leukoencephalopathy syndrome and silent cerebral infarcts are associated with severe acute chest syndrome in children with sickle cell disease
43. Decline in Forced Expiratory Volume in 1 Second in Older Adults with Sickle Cell Disease Is Similar to Adults with Cystic Fibrosis
44. High Levels of Peripheral Vasoconstriction Detected By Polysomnography Predict More Acute Severe Pain Episodes in Children with Sickle Cell Anemia
45. Cross Sectional Survey of Priapism and Sexual Dysfunction in 353 Men with Sickle Cell Disease
46. Reduced Intensity Conditioning for Haploidentical Bone Marrow Transplantation in Patients with Symptomatic Sickle Cell Disease: BMT CTN Protocol 1507
47. Sickle Cell Disease Post-Transplant Care Challenges in Nigeria: Systematic Institutional Neglect of Medical Tourism
48. Primary Prevention of Strokes in Nigerian Children with Sickle Cell Disease (SPIN Trial): Final Results
49. Longitudinal changes in brain magnetic resonance imaging findings in children with sickle cell disease
50. Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia
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