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Prague Medical Report|September 18, 2025
Glucocorticoid Remediable Aldosteronism in a Family with a Strong History of Cerebral Aneurysms and HypertensionJan Zeman, Crystal Kamilaris
Endocrinology, Diabetes & Metabolism Case Reports|August 7, 2020
Curative resection of an aldosteronoma causing primary aldosteronism in the second trimester of pregnancySkand Shekhar, Rasha Haykal, Crystal Kamilaris, et al.
The Lancet. Child & Adolescent Health|December 14, 2023
Paediatric Cushing syndrome: a prospective, multisite, observational cohort studyChristina Tatsi, Crystal Kamilaris, Meg Keil, et al.
Endocrinology, Diabetes & Metabolism Case Reports|June 2, 2020
Inhibin A as a tumor marker for primary bilateral macronodular adrenal hyperplasiaRachel Wurth, Crystal Kamilaris, Naris Nilubol, et al.
American Journal of Hypertension|October 23, 2019
Mosaicism for KCNJ5 Causing Early-Onset Primary Aldosteronism due to Bilateral Adrenocortical HyperplasiaAndrea G Maria, Mari Suzuki, Annabel Berthon, et al.
Endocrinology, Diabetes & Metabolism Case Reports|April 11, 2021
A case of Carney triad complicated by renal cell carcinoma and a germline SDHA pathogenic variantRachel Wurth, Abhishek Jha, Crystal Kamilaris, et al.
The Journal of Investigative Dermatology|May 14, 2022
Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex SyndromeIsabelle Sahut-Barnola, Anne-Marie Lefrançois-Martinez, Damien Dufour, et al.
The Journal of Clinical Investigation|December 1, 2021
Protein kinase A drives paracrine crisis and WNT4-dependent testis tumor in Carney complexCyril Djari, Isabelle Sahut-Barnola, Amandine Septier, et al.
European Journal of Endocrinology|February 8, 2025
KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlationLucas Bouys, Patricia Vaduva, Anne Jouinot, et al.
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