These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
159 related items for PubMed ID: 1756212
1. Normal sequence of the gonadotropin-releasing hormone gene in patients with idiopathic hypogonadotropic hypogonadism. Weiss J, Adams E, Whitcomb RW, Crowley WF, Jameson JL. Biol Reprod; 1991 Nov; 45(5):743-7. PubMed ID: 1756212 [Abstract] [Full Text] [Related]
8. Exaggerated free alpha-subunit levels during pulsatile gonadotropin-releasing hormone replacement in women with idiopathic hypogonadotropic hypogonadism. Lavoie HB, Martin KA, Taylor E, Crowley WF, Hall JE. J Clin Endocrinol Metab; 1998 Jan; 83(1):241-7. PubMed ID: 9435449 [Abstract] [Full Text] [Related]
9. Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation. Bouligand J, Ghervan C, Tello JA, Brailly-Tabard S, Salenave S, Chanson P, Lombès M, Millar RP, Guiochon-Mantel A, Young J. N Engl J Med; 2009 Jun 25; 360(26):2742-8. PubMed ID: 19535795 [Abstract] [Full Text] [Related]
11. Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice. Falardeau J, Chung WC, Beenken A, Raivio T, Plummer L, Sidis Y, Jacobson-Dickman EE, Eliseenkova AV, Ma J, Dwyer A, Quinton R, Na S, Hall JE, Huot C, Alois N, Pearce SH, Cole LW, Hughes V, Mohammadi M, Tsai P, Pitteloud N. J Clin Invest; 2008 Aug 25; 118(8):2822-31. PubMed ID: 18596921 [Abstract] [Full Text] [Related]
12. The same molecular defects of the gonadotropin-releasing hormone receptor determine a variable degree of hypogonadism in affected kindred. de Roux N, Young J, Brailly-Tabard S, Misrahi M, Milgrom E, Schaison G. J Clin Endocrinol Metab; 1999 Feb 25; 84(2):567-72. PubMed ID: 10022417 [Abstract] [Full Text] [Related]
13. 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, Seminara SB. J Clin Endocrinol Metab; 2001 Apr 25; 86(4):1580-8. PubMed ID: 11297587 [Abstract] [Full Text] [Related]
14. The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. Waldstreicher J, Seminara SB, Jameson JL, Geyer A, Nachtigall LB, Boepple PA, Holmes LB, Crowley WF. J Clin Endocrinol Metab; 1996 Dec 25; 81(12):4388-95. PubMed ID: 8954047 [Abstract] [Full Text] [Related]
15. [GnRH deficiency: new insights from genetics]. Kottler ML, Hamel A, Malville E, Richard N. J Soc Biol; 2004 Dec 25; 198(1):80-7. PubMed ID: 15146960 [Abstract] [Full Text] [Related]
16. GNRHR mutations in a woman with idiopathic hypogonadotropic hypogonadism highlight the differential sensitivity of luteinizing hormone and follicle-stimulating hormone to gonadotropin-releasing hormone. Meysing AU, Kanasaki H, Bedecarrats GY, Acierno JS, Conn PM, Martin KA, Seminara SB, Hall JE, Crowley WF, Kaiser UB. J Clin Endocrinol Metab; 2004 Jul 25; 89(7):3189-98. PubMed ID: 15240592 [Abstract] [Full Text] [Related]
17. Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: evidence that DAX-1 mutations lead to combined hypothalmic and pituitary defects in gonadotropin production. Habiby RL, Boepple P, Nachtigall L, Sluss PM, Crowley WF, Jameson JL. J Clin Invest; 1996 Aug 15; 98(4):1055-62. PubMed ID: 8770879 [Abstract] [Full Text] [Related]
18. Responsiveness to a physiological regimen of GnRH therapy and relation to genotype in women with isolated hypogonadotropic hypogonadism. Abel BS, Shaw ND, Brown JM, Adams JM, Alati T, Martin KA, Pitteloud N, Seminara SB, Plummer L, Pignatelli D, Crowley WF, Welt CK, Hall JE. J Clin Endocrinol Metab; 2013 Feb 15; 98(2):E206-16. PubMed ID: 23341491 [Abstract] [Full Text] [Related]
19. Clinical manifestations of impaired GnRH neuron development and function. Kim HG, Bhagavath B, Layman LC. Neurosignals; 2008 Feb 15; 16(2-3):165-82. PubMed ID: 18253056 [Abstract] [Full Text] [Related]
20. Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH). Miura K, Acierno JS, Seminara SB. J Hum Genet; 2004 Feb 15; 49(5):265-8. PubMed ID: 15362570 [Abstract] [Full Text] [Related] Page: [Next] [New Search]