Showing results (41-50 of 60) with videos related to
Sort By:
Pageof 6
Journal of Pediatric Surgery|December 6, 2014
Surgical treatment of children with hyperparathyroidism: single centre experienceS Alagaratnam, C Brain, H Spoudeas, et al.Heart (British Cardiac Society)|August 11, 2007
Hypocalcaemia and vitamin D deficiency: an important, but preventable, cause of life-threatening infant heart failureS Maiya, I Sullivan, J Allgrove, et al.Cancer Chemotherapy and Pharmacology|November 16, 2006
Variations in schedules of ifosfamide administration: a better understanding of its implications on pharmacokinetics through a randomized cross-over studyE G C Brain, K Rezai, S Weill, et al.Journal of the American Medical Informatics Association : JAMIA|March 27, 2023
Evaluating the costs and consequences of computerized clinical decision support systems in hospitals: a scoping review and recommendations for future practiceNicole M White, Hannah E Carter, Sanjeewa Kularatna, et al.JAMA|May 19, 2005
Life-threatening sepsis associated with adjuvant doxorubicin plus docetaxel for intermediate-risk breast cancerEtienne G C Brain, Thomas Bachelot, Daniel Serin, et al.Clinical Nutrition (Edinburgh, Scotland)|October 14, 2018
Elemental formula associated hypophosphataemic ricketsS Uday, S Sakka, J H Davies, et al.Journal of Cancer Research and Clinical Oncology|January 1, 1997
6-Day continuous infusion of high-dose ifosfamide with bone marrow growth factors in advanced refractory malignanciesE C Brain, A Mita, P Soulié, et al.Human Molecular Genetics|August 1, 1995
A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasiaL Laue, S M Wu, M Kudo, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 20, 2010
Anthracycline cardiotoxicity in the elderly cancer patient: a SIOG expert position paperM Aapro, C Bernard-Marty, E G C Brain, et al.Molecular Endocrinology (Baltimore, Md.)|November 17, 1998
Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasiaS M Wu, K M Hallermeier, L Laue, et al.Pageof 6