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Diabetes Research and Clinical Practice|June 23, 2016
Clinical and genetic features of Argentinian children with diabetes-onset before 12months of age: Successful transfer from insulin to oral sulfonylureaPatricia Taberner, Sarah E Flanagan, Deborah J Mackay, et al.
Journal of Burn Care & Research : Official Publication of the American Burn Association|December 6, 2011
When a hero becomes a patient: firefighter burn injuries in the National Burn RepositorySarah E Matt, Jeffery W Shupp, Elizabeth A Carter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 29, 2013
Activating AKT2 mutation: hypoinsulinemic hypoketotic hypoglycemiaVed Bhushan Arya, Sarah E Flanagan, Edith Schober, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2019
A rare case of congenital hyperinsulinism (CHI) due to dual genetic aetiology involving HNF4A and ABCC8Louise Apperley, Dinesh Giri, Jayne A L Houghton, et al.
Human Mutation|April 14, 2025
REVEL Is Better at Predicting Pathogenicity of Loss-of-Function than Gain-of-Function VariantsJasmin J Hopkins, Matthew N Wakeling, Matthew B Johnson, et al.
BMJ Quality & Safety|July 30, 2015
"Mr Smith's been our problem child today…": anticipatory management communication (AMC) in VA end-of-shift medicine and nursing handoffsAlicia A Bergman, Mindy E Flanagan, Patricia R Ebright, et al.
Skin Appendage Disorders|October 4, 2021
Hair Growth in a Patient with Alopecia Areata on TocilizumabChloe J Walker, Kelly E Flanagan, James T Pathoulas, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 12, 2014
Three cases of Wolfram syndrome with different clinical aspectsEmine Çamtosun, Zeynep Şıklar, Pınar Kocaay, et al.
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