Showing results (71-80 of 108) with videos related to
Sort By:
Pageof 11
Clinical Practice in Pediatric Psychology|March 21, 2022
Fertility Discussions: Perspectives of Adolescents and Young Adults With Differences of Sex DevelopmentJaclyn L Papadakis, Jonathan L Poquiz, Cindy L Buchanan, et al.Hormone Research in Paediatrics|April 15, 2010
Central precocious puberty due to hypothalamic hamartomas correlates with anatomic features but not with expression of GnRH, TGFalpha, or KISS1Yee-Ming Chan, Kristina A Fenoglio-Simeone, Sophia Paraschos, et al.Endocrinology|June 1, 2014
Implantation failure in female Kiss1-/- mice is independent of their hypogonadic state and can be partially rescued by leukemia inhibitory factorMichele Calder, Yee-Ming Chan, Renju Raj, et al.Biorxiv : the Preprint Server for Biology|October 17, 2024
Independent effects of testosterone, estradiol, and sex chromosomes on gene expression in immune cells of trans- and cisgender individualsRebecca M Harris, Troy Whitfield, Laura V Blanton, et al.Proceedings of the National Academy of Sciences of the United States of America|July 2, 2009
GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadismYee-Ming Chan, Adelaide de Guillebon, Mariarosaria Lang-Muritano, et al.The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine systemValerie F Sidhoum, Yee-Ming Chan, Margaret F Lippincott, et al.Nature Reviews. Disease Primers|June 1, 2019
Paediatric and adult-onset male hypogonadismAndrea Salonia, Giulia Rastrelli, Geoffrey Hackett, et al.Journal of Pediatric Psychology|June 10, 2024
Trajectories of illness uncertainty among parents of children with atypical genital appearance due to differences of sex developmentKatherine A Traino, Lucia M Ciciolla, Megan N Perez, et al.Behavior Genetics|February 21, 2018
The Biological Contributions to Gender Identity and Gender Diversity: Bringing Data to the TableTinca J C Polderman, Baudewijntje P C Kreukels, Michael S Irwig, et al.European Journal of Human Genetics : EJHG|February 2, 2021
Novel variants in the stem cell niche factor WNT2B define the disease phenotype as a congenital enteropathy with ocular dysgenesisYanjia Jason Zhang, Lissette Jimenez, Svetlana Azova, et al.Pageof 11