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151. Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

154. Contributors

156. List of Contributors

159. Contributors

161. Contributors

172. 6. A MULTICENTER CLUSTER RANDOMIZED CONTROLLED TRIAL OF A NOVEL MINDFULNESS CURRICULUM DURING PEDIATRIC INTERNSHIP

175. Persistent Disease Activity in Patients With Long-Standing Glomerular Disease

178. Diagnosis, Treatment, and Outcomes in Children With Congenital Nephrogenic Diabetes Insipidus: A Pediatric Nephrology Research Consortium Study

180. Predicting and Defining Steroid Resistance in Pediatric Nephrotic Syndrome Using Plasma Proteomics

181. Predicting and Defining Steroid Resistance in Pediatric Nephrotic Syndrome Using Plasma Metabolomics

182. Agreement of Program Directors With Clinical Competency Committees for Fellow Entrustment

183. Health-related quality of life in glomerular disease

188. Health Care Transition From Pediatric- to Adult-Focused Care in X-linked Hypophosphatemia: Expert Consensus.

189. An Initiative to Increase Residency Program Diversity.

194. The van der Waals epitaxial growth of GaSe on Si(111)

198. Epitaxial ternary RexMo1-xSi2 thin films on Si(100)

200. Surface electron-diffraction patterns of beta-FeSi2 films epitaxially grown on silicon

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