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Page 1
A genetic basis for functional hypothalamic amenorrhea.
Caronia LM, Martin C, Welt CK, Sykiotis GP, Quinton R, Thambundit A, Avbelj M, Dhruvakumar S, Plummer L, Hughes VA, Seminara SB, Boepple PA, Sidis Y, Crowley WF Jr, Martin KA, Hall JE, Pitteloud N. Caronia LM, et al. Among authors: pitteloud n. N Engl J Med. 2011 Jan 20;364(3):215-25. doi: 10.1056/NEJMoa0911064. N Engl J Med. 2011. PMID: 21247312 Free PMC article.
Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism.
Beranova M, Oliveira LM, Bédécarrats GY, Schipani E, Vallejo M, Ammini AC, Quintos JB, Hall JE, Martin KA, Hayes FJ, Pitteloud N, Kaiser UB, Crowley WF Jr, Seminara SB. Beranova M, et al. Among authors: pitteloud n. J Clin Endocrinol Metab. 2001 Apr;86(4):1580-8. doi: 10.1210/jcem.86.4.7395. J Clin Endocrinol Metab. 2001. PMID: 11297587 Free article.
Kallmann syndrome in a 47,XXX patient.
Corssmit EP, Seminara SB, Pitteloud N, Fliers E. Corssmit EP, et al. Among authors: pitteloud n. Am J Med Genet A. 2005 Nov 15;139(1):52-3. doi: 10.1002/ajmg.a.30996. Am J Med Genet A. 2005. PMID: 16222664 No abstract available.
155 results