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The New England Journal of Medicine|May 10, 2013
Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitinationDavid H Margolin, Maria Kousi, Yee-Ming Chan, et al.Journal of Pediatric Urology|July 7, 2020
Post-operative complications following feminizing genitoplasty in moderate to severe genital atypia: Results from a multicenter, observational prospective cohort studyAvi Baskin, Amy B Wisniewski, Christopher E Aston, et al.Journal of Pediatric and Adolescent Gynecology|August 10, 2022
Exploring Factors Associated with Decisions about Feminizing Genitoplasty in Differences of Sex DevelopmentJessica Kremen, Rebecca M Harris, Christopher E Aston, et al.Hormone Research in Paediatrics|February 4, 2024
Multi-Stakeholder Opinion Statement on the Care of Individuals Born with Differences of Sex Development: Common Ground and Opportunities for ImprovementMartine Cools, Earl Y Cheng, Joanne Hall, et al.Human Molecular Genetics|July 5, 2020
TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal lociErica E Davis, Ravikumar Balasubramanian, Zachary A Kupchinsky, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|March 30, 2022
Stigma, Intrusiveness, and Distress in Parents of Children with a Disorder/Difference of Sex DevelopmentKatherine A Traino, Caroline M Roberts, Rachel S Fisher, et al.The Journal of Urology|July 4, 2019
Predictors of Psychosocial Distress in Parents of Young Children with Disorders of Sex DevelopmentMegan N Perez, Alexandria M Delozier, Christopher E Aston, et al.Journal of Pediatric Psychology|February 17, 2021
Distress Trajectories for Parents of Children With DSD: A Growth Mixture ModelMegan N Perez, Ashley H Clawson, Marissa N Baudino, et al.Journal of the Endocrine Society|January 10, 2019
Baseline Characteristics of Infants With Atypical Genital Development: Phenotypes, Diagnoses, and Sex of RearingCourtney Finlayson, Ilina Rosoklija, Christopher E Aston, et al.The Journal of Clinical Endocrinology and Metabolism|September 2, 2011
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1Yee-Ming Chan, Sarabeth Broder-Fingert, Sophia Paraschos, et al.Pageof 11