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European Journal of Pediatrics|June 13, 2008
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2--initial and long-term response to sulfonylurea therapyVerena M Wagner, Britta Kremke, Olaf Hiort, et al.The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association|May 20, 2024
Early Play Behaviors of Infants at Elevated Likelihood for Autism Spectrum DisorderJoanne E Flanagan, Barbara B Demchick, Rebecca Landa, et al.Journal of Cutaneous Pathology|May 13, 2021
Sweet syndrome with perifollicular involvement because of koebnerization from facial hair pluckingKelly E Flanagan, Steven Krueger, Shinya Amano, et al.American Journal of Infection Control|July 22, 2011
Reducing health care-associated infections (HAIs): lessons learned from a national collaborative of regional HAI programsCatherine Amber Welsh, Mindy E Flanagan, Shawn C Hoke, et al.The Journal of Clinical Endocrinology and Metabolism|May 7, 2009
3-Hydroxyacyl-coenzyme A dehydrogenase deficiency and hyperinsulinemic hypoglycemia: characterization of a novel mutation and severe dietary protein sensitivityRitika R Kapoor, Chela James, Sarah E Flanagan, et al.AMIA ... Annual Symposium Proceedings. AMIA Symposium|February 20, 2014
Multihospital infection prevention collaborative: informatics challenges and strategies to prevent MRSABradley N Doebbeling, Mindy E Flanagan, Glenna Nall, et al.Journal of the American Medical Informatics Association : JAMIA|April 20, 2013
The next-generation electronic health record: perspectives of key leaders from the US Department of Veterans AffairsJason J Saleem, Mindy E Flanagan, Nancy R Wilck, et al.Ophthalmic Plastic and Reconstructive Surgery|March 21, 2009
High versus low concentration botulinum toxin A for benign essential blepharospasm: does dilution make a difference?Michael H Boyle, Gerald McGwin, Courtney E Flanagan, et al.Diabetes Research and Clinical Practice|October 14, 2014
Permanent neonatal diabetes misdiagnosed as type 1 diabetes in a 28-year-old female: a life-changing diagnosisYotsapon Thewjitcharoen, Ekgaluck Wanothayaroj, Thep Himathongkam, et al.Human Molecular Genetics|December 22, 2009
Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptomsRoope Männikkö, Craig Jefferies, Sarah E Flanagan, et al.Pageof 51