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Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline.
Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, Merke DP, Meyer-Bahlburg HF, Miller WL, Montori VM, Oberfield SE, Ritzen M, White PC; Endocrine Society. Speiser PW, et al. Among authors: ritzen m. J Clin Endocrinol Metab. 2010 Sep;95(9):4133-60. doi: 10.1210/jc.2009-2631. J Clin Endocrinol Metab. 2010. PMID: 20823466 Free PMC article.
A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency.
Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, Merke DP, Meyer-Bahlburg HF, Miller WL, Montori VM, Oberfield SE, Ritzen M, White PC. Speiser PW, et al. Among authors: ritzen m. Int J Pediatr Endocrinol. 2010;2010:494173. doi: 10.1155/2010/494173. Epub 2010 Jun 30. Int J Pediatr Endocrinol. 2010. PMID: 20981249 Free PMC article.
Recommendations for the diagnosis and management of Prader-Willi syndrome.
Goldstone AP, Holland AJ, Hauffa BP, Hokken-Koelega AC, Tauber M; speakers contributors at the Second Expert Meeting of the Comprehensive Care of Patients with PWS. Goldstone AP, et al. J Clin Endocrinol Metab. 2008 Nov;93(11):4183-97. doi: 10.1210/jc.2008-0649. Epub 2008 Aug 12. J Clin Endocrinol Metab. 2008. PMID: 18697869
Serum androgen levels in elite female athletes.
Bermon S, Garnier PY, Hirschberg AL, Robinson N, Giraud S, Nicoli R, Baume N, Saugy M, Fénichel P, Bruce SJ, Henry H, Dollé G, Ritzen M. Bermon S, et al. Among authors: ritzen m. J Clin Endocrinol Metab. 2014 Nov;99(11):4328-35. doi: 10.1210/jc.2014-1391. Epub 2014 Aug 19. J Clin Endocrinol Metab. 2014. PMID: 25137421
98 results