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Page 1
Topical triamcinolone induced Cushing syndrome: A case report.
Taylor O, Mejia-Otero JD, Tannin GM, Gordon K. Taylor O, et al. Among authors: tannin gm. Pediatr Dermatol. 2020 May;37(3):582-584. doi: 10.1111/pde.14140. Epub 2020 Mar 24. Pediatr Dermatol. 2020. PMID: 32212183
Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene.
Kayes-Wandover KM, Tannin GM, Shulman D, Peled D, Jones KL, Karaviti L, White PC. Kayes-Wandover KM, et al. Among authors: tannin gm. J Clin Endocrinol Metab. 2001 Nov;86(11):5379-82. doi: 10.1210/jcem.86.11.8005. J Clin Endocrinol Metab. 2001. PMID: 11701710 Clinical Trial.
Genetic analysis of 11 beta-hydroxysteroid dehydrogenase.
White PC, Obeid J, Agarwal AK, Tannin GM, Nikkila H. White PC, et al. Among authors: tannin gm. Steroids. 1994 Feb;59(2):111-5. doi: 10.1016/0039-128x(94)90086-8. Steroids. 1994. PMID: 8191538 Review.
Defects in the HSD11 gene encoding 11 beta-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency.
Nikkilä H, Tannin GM, New MI, Taylor NF, Kalaitzoglou G, Monder C, White PC. Nikkilä H, et al. Among authors: tannin gm. J Clin Endocrinol Metab. 1993 Sep;77(3):687-91. doi: 10.1210/jcem.77.3.8370690. J Clin Endocrinol Metab. 1993. PMID: 8370690