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Response to challenge with gonadotropin-releasing hormone agonist in a mother and her two sons with a constitutively activating mutation of the luteinizing hormone receptor--a clinical research center study.
Rosenthal IM, Refetoff S, Rich B, Barnes RB, Sunthornthepvarakul T, Parma J, Rosenfield RL. Rosenthal IM, et al. Among authors: rich b. J Clin Endocrinol Metab. 1996 Oct;81(10):3802-6. doi: 10.1210/jcem.81.10.8855841. J Clin Endocrinol Metab. 1996. PMID: 8855841
A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia.
Pang S, Wang W, Rich B, David R, Chang YT, Carbunaru G, Myers SE, Howie AF, Smillie KJ, Mason JI. Pang S, et al. Among authors: rich b. J Clin Endocrinol Metab. 2002 Jun;87(6):2556-63. doi: 10.1210/jcem.87.6.8559. J Clin Endocrinol Metab. 2002. PMID: 12050213
Adrenarche: changing adrenal response to adrenocorticotropin.
Rich BH, Rosenfield RL, Lucky AW, Helke JC, Otto P. Rich BH, et al. J Clin Endocrinol Metab. 1981 Jun;52(6):1129-36. doi: 10.1210/jcem-52-6-1129. J Clin Endocrinol Metab. 1981. PMID: 6262366 No abstract available.
Adrenarche as a cause of benign pseudopuberty in boys.
Rosenfield RL, Rich BH, Lucky AW. Rosenfield RL, et al. Among authors: rich bh. J Pediatr. 1982 Dec;101(6):1005-9. doi: 10.1016/s0022-3476(82)80033-4. J Pediatr. 1982. PMID: 6216332
386 results