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Proceedings of the National Academy of Sciences of the United States of America|November 21, 2007
Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetesHeidi de Wet, Mathew G Rees, Kenju Shimomura, et al.Infection Control and Hospital Epidemiology|July 1, 2010
Observer bias in hand hygiene compliance reportingSorabh Dhar, Ryan Tansek, Elizabeth A Toftey, et al.Pediatric Diabetes|June 6, 2009
Incidence of neonatal diabetes in Austria-calculation based on the Austrian Diabetes RegisterBarbara Wiedemann, Edith Schober, Thomas Waldhoer, et al.Pediatric Diabetes|February 29, 2012
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemiaCharles Shaw-Smith, Sarah E Flanagan, Ann-Marie Patch, et al.Frontiers in Endocrinology|March 5, 2025
Large copy number variants are an important cause of congenital hyperinsulinism that should be screened for during routine testingSarah E Flanagan, Isabella-Anna Lazaridi, Jonna M E Männistö, et al.Journal of Neuropathology and Experimental Neurology|April 16, 2026
Vascular burden attenuates the TDP-43-TMEM106B pathological relationship in neurodegenerative disease with and without Alzheimer disease neuropathological changeMatthew B Dopler, Cole Corbett, Angelique D Gonzalez, et al.Autism Research : Official Journal of the International Society for Autism Research|January 12, 2019
Comparing the 1-year impact of preschool autism intervention programs in two Canadian provincesIsabel M Smith, Helen E Flanagan, Wendy J Ungar, et al.Journal of Clinical Immunology|January 4, 2023
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX SyndromeRebecca C Wyatt, Sven Olek, Elisa De Franco, et al.Diabetic Medicine : a Journal of the British Diabetic Association|June 16, 2010
Entities and frequency of neonatal diabetes: data from the diabetes documentation and quality management system (DPV)J Grulich-Henn, V Wagner, A Thon, et al.Diabetes|April 21, 2007
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthoodSarah E Flanagan, Ann-Marie Patch, Deborah J G Mackay, et al.Pageof 51