1,849 results on '"DeBaun, Michael"'
Search Results
152. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease
153. Leukemia after gene therapy for sickle cell disease: insertional mutagenesis, busulfan, both, or neither
154. Increased circulating fibrocytes are associated with higher reticulocyte percent in children with sickle cell anemia
155. Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years
156. A cross-sectional study of bleeding phenotype in haemophilia A carriers
157. Increased risk of severe vaso-occlusive episodes after initial acute chest syndrome in children with sickle cell anemia less than 4 years old: Sleep and asthma cohort
158. 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
159. Cerebral Blood Flow, Brain Volume, and Age Predicts Executive Function in Sickle Cell Anemia
160. Histopathology of experimentally induced asthma in a murine model of sickle cell disease
161. Enuresis Is a Common and Persistent Problem Among Children and Young Adults with Sickle Cell Anemia
162. Primary stroke prevention in Nigerian children with sickle cell disease (SPIN): Challenges of conducting a feasibility trial
163. Health-related quality of life in children with sickle cell anemia: Impact of blood transfusion therapy
164. Coronary Artery Dilation and Left Ventricular Hypertrophy Do Not Predict Morbidity in Children With Sickle Cell Disease
165. Factors associated with growth and blood pressure patterns in children with sickle cell anemia: Silent Cerebral Infarct Multi-Center Clinical Trial cohort
166. Incidental findings on brain magnetic resonance imaging of children with sickle cell disease
167. Hydroxyurea therapy contributes to infertility in adult men with sickle cell disease: a review
168. Thinking beyond survival
169. Transfusions for Silent Cerebral Infarcts in Sickle Cell Anemia
170. Factors predicting future ACS episodes in children with sickle cell anemia
171. Silent cerebral infarction, income, and grade retention among students with sickle cell anemia
172. The Challenge of Creating an Evidence-Based Guideline for Sickle Cell Disease
173. Imbalanced coagulation profile as a biomarker of migraine in children with sickle cell: Is this a link with cerebral ischemia?
174. Controlled Trial of Transfusions for Silent Cerebral Infarcts in Sickle Cell Anemia
175. Females with FVIII and FIX deficiency have reduced joint range of motion
176. Initiating adjunct low-dose hydroxyurea therapy for stroke prevention in children with SCA during the COVID-19 pandemic
177. Nocturnal enuresis in sickle cell disease
178. Silent Cerebral Infarct Transfusion (SIT) Trial Imaging Core: Application of Novel Imaging Information Technology for Rapid and Central Review of MRI of the Brain
179. Academic Medicine’s Journey Toward Racial Equity Must Be Grounded in History: Recommendations for Becoming an Antiracist Academic Medical Center
180. Correction: The american pediatric society and society for pediatric research joint statement against racism and social injustice
181. Identifying Elevated Risk for Future Pain Crises in Sickle-Cell Disease Using Photoplethysmogram Patterns Measured During Sleep: A Machine Learning Approach
182. Author Response: Distribution of Silent Cerebral Infarcts in Adults With Sickle Cell Disease
183. Cerebral Hemodynamic Responses to Disease-Modifying and Curative Sickle Cell Disease Therapies
184. Reduction in TCD velocity after regular blood transfusion therapy is associated with a change in hemoglobin S fraction in sickle cell anemia
185. Primary Analysis of Spartan: A Phase 2 Trial to Assess the Efficacy and Safety of Crizanlizumab in Patients with Sickle Cell Disease Related Priapism
186. 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
187. 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
188. 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
189. Localization of Silent Cerebral Infarcts in Children with Sickle Cell Disease Impacts Structural Disconnection
190. A Working Definition of Acute Chest Syndrome without the Requirement of Chest X-Rays
191. 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
192. Characterization of Sickle Cell Disease Mortality in a National Electronic Health Record (EHR) System
193. Assessing Pain Severity in Sickle Cell Disease Using Animations and a Graphical Body Image
194. A Genotype Validated Bimodal Method for the Large-Scale Identification and Phenotyping of Persons with Sickle Cell Disease Using Electronic Health Record Data
195. A Randomized Clinical Trial Testing the Effect of Digital Behavioral Interventions on Pain and Mental Health Among Adults with Sickle Cell Disease
196. Risk for postterm delivery after previous postterm delivery
197. Racial disparity in the frequency of recurrence of preterm birth
198. Primary hemorrhagic stroke in children with sickle cell disease is associated with recent transfusion and use of corticosteroids
199. A multidisciplinary health care team's efforts to improve educational attainment in children with sickle-cell anemia and cerebral infarcts
200. Academic pipeline initiatives in pediatrics
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