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Plos Medicine|February 25, 2021
Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization studyDespoina Manousaki, Adil Harroud, Ruth E Mitchell, et al.Plos Medicine|April 29, 2021
Correction: Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization studyDespoina Manousaki, Adil Harroud, Ruth E Mitchell, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|January 10, 2018
Improved medical-alert ID ownership and utilization in youth with congenital adrenal hyperplasia following a parent educational interventionAlaina P Vidmar, Jonathan F Weber, Roshanak Monzavi, et al.The Journal of Clinical Endocrinology and Metabolism|February 4, 2021
Monogenic Causes in the Type 1 Diabetes Genetics Consortium Cohort: Low Genetic Risk for Autoimmunity in Case SelectionLuc Marchand, Meihang Li, Coralie Leblicq, et al.The Journal of Clinical Endocrinology and Metabolism|June 11, 2014
Presence of brown adipose tissue in an adolescent with severe primary hypothyroidismMimi S Kim, Houchun H Hu, Patricia C Aggabao, et al.European Journal of Endocrinology|November 18, 2021
Prevalence and phenotypic features of diabetes due to recessive, non-syndromic WFS1 mutationsMingqiang Zhu, Yangxi Li, Guanping Dong, et al.Hormone Research in Paediatrics|November 25, 2016
Guidelines for Growth Hormone and Insulin-Like Growth Factor-I Treatment in Children and Adolescents: Growth Hormone Deficiency, Idiopathic Short Stature, and Primary Insulin-Like Growth Factor-I DeficiencyAdda Grimberg, Sara A DiVall, Constantin Polychronakos, et al.American Journal of Physiology. Endocrinology and Metabolism|April 30, 2009
Leucine restriction inhibits chondrocyte proliferation and differentiation through mechanisms both dependent and independent of mTOR signalingMimi S Kim, Ke Ying Wu, Valerie Auyeung, et al.Journal of Medical Genetics|October 15, 2013
Somatic point mutations occurring early in development: a monozygotic twin studyRui Li, Alexandre Montpetit, Marylène Rousseau, et al.Journal of Investigative Medicine High Impact Case Reports|September 26, 2022
A Unique Case of Aggressive Central Giant Cell Granuloma in a 10-Year-Old Boy With 16p13.11 Microdeletion SyndromeBetty J Shum, Mimi S Kim, Katelyn Kondra, et al.Pageof 16