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The Journal of Pediatrics|April 16, 2008
Insulin resistance, hyperinsulinemia, and energy intake in overweight childrenJoan C Han, Margaret S Rutledge, Merel Kozlosky, et al.The Journal of Clinical Endocrinology and Metabolism|March 3, 2005
Children experience cognitive decline despite reversal of brain atrophy one year after resolution of Cushing syndromeDeborah P Merke, Jay N Giedd, Margaret F Keil, et al.The Journal of Clinical Endocrinology and Metabolism|December 13, 2024
Adult Height Following Prepubertal Treatment With Antiandrogen, Aromatase Inhibitor, and Reduced Hydrocortisone in CAHDeborah P Merke, Ashwini Mallappa, Megan Parker, et al.The Journal of Clinical Endocrinology and Metabolism|April 2, 2020
Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 PhenotypeFanny Chasseloup, Nathan Pankratz, John Lane, et al.Brain Research Bulletin|April 14, 2018
Mice deficient in AKAP13 (BRX) develop compulsive-like behavior and increased body weightK Maravet Baig, Szu-Chi Su, Sunni L Mumford, et al.The Journal of Clinical Endocrinology and Metabolism|June 5, 2019
Germline USP8 Mutation Associated With Pediatric Cushing Disease and Other Clinical Features: A New SyndromeMichal Cohen, Rebecca Persky, Rachel Stegemann, et al.The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
The stability of metabolic syndrome in children and adolescentsJennifer K Gustafson, Lisa B Yanoff, Benjamin D Easter, et al.The Journal of Clinical Endocrinology and Metabolism|October 31, 2013
Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testingParaskevi Salpea, Anelia Horvath, Edra London, et al.Frontiers in Endocrinology|July 28, 2020
Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?Idoia Martínez de LaPiscina, Laura C Hernández-Ramírez, Nancy Portillo, et al.The New England Journal of Medicine|December 4, 2014
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutationGiampaolo Trivellin, Adrian F Daly, Fabio R Faucz, et al.Pageof 5