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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1975 2
1976 3
1977 3
1978 4
1979 4
1980 4
1981 3
1982 1
1983 3
1984 5
1985 11
1986 2
1987 13
1988 8
1989 5
1990 5
1991 8
1992 8
1993 5
1994 12
1995 12
1996 10
1997 6
1998 13
1999 11
2000 18
2001 10
2002 19
2003 13
2004 17
2005 24
2006 13
2007 22
2008 22
2009 27
2010 34
2011 36
2012 22
2013 27
2014 40
2015 53
2016 37
2017 37
2018 38
2019 53
2020 46
2021 55
2022 70
2023 51
2024 11

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845 results

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Page 1
Anabolic steroid-induced hypogonadism: diagnosis and treatment.
Rahnema CD, Lipshultz LI, Crosnoe LE, Kovac JR, Kim ED. Rahnema CD, et al. Fertil Steril. 2014 May;101(5):1271-9. doi: 10.1016/j.fertnstert.2014.02.002. Epub 2014 Mar 14. Fertil Steril. 2014. PMID: 24636400 Free article. Review.
Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism.
Stamou MI, Georgopoulos NA. Stamou MI, et al. Metabolism. 2018 Sep;86:124-134. doi: 10.1016/j.metabol.2017.10.012. Epub 2017 Nov 3. Metabolism. 2018. PMID: 29108899 Free PMC article. Review.
The clinical spectrum of IGD includes a variety of disorders including Kallmann Syndrome (KS), i.e. hypogonadotropic hypogonadism with anosmia, and its normosmic variation normosmic idiopathic hypogonadotropic hypogonadism (nIHH), which represent the m …
The clinical spectrum of IGD includes a variety of disorders including Kallmann Syndrome (KS), i.e. hypogonadotropic hypogonadism
Male and Female Hypogonadism.
Richard-Eaglin A. Richard-Eaglin A. Nurs Clin North Am. 2018 Sep;53(3):395-405. doi: 10.1016/j.cnur.2018.04.006. Nurs Clin North Am. 2018. PMID: 30100005 Review.
Clinical Management of Congenital Hypogonadotropic Hypogonadism.
Young J, Xu C, Papadakis GE, Acierno JS, Maione L, Hietamäki J, Raivio T, Pitteloud N. Young J, et al. Endocr Rev. 2019 Apr 1;40(2):669-710. doi: 10.1210/er.2018-00116. Endocr Rev. 2019. PMID: 30698671 Review.
The initiation and maintenance of reproductive capacity in humans is dependent on pulsatile secretion of the hypothalamic hormone GnRH. Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder that results from the failure of the normal episodic GnRH secret …
The initiation and maintenance of reproductive capacity in humans is dependent on pulsatile secretion of the hypothalamic hormone GnRH. Cong …
Genetics of Azoospermia.
Cioppi F, Rosta V, Krausz C. Cioppi F, et al. Int J Mol Sci. 2021 Mar 23;22(6):3264. doi: 10.3390/ijms22063264. Int J Mol Sci. 2021. PMID: 33806855 Free PMC article. Review.
Delayed puberty.
Butler G, Purushothaman P. Butler G, et al. Minerva Pediatr. 2020 Dec;72(6):484-490. doi: 10.23736/S0026-4946.20.05968-X. Epub 2020 Aug 4. Minerva Pediatr. 2020. PMID: 32748610 Review.
Investigations should be targeted at ruling out any medical causes and determining whether the delay is due to central gonadotropin deficiency (hypogonadotropic hypogonadism) or a gonadal disorder (hypergonadotropic hypogonadism). Physiological or constitutional del …
Investigations should be targeted at ruling out any medical causes and determining whether the delay is due to central gonadotropin deficien …
Hypogonadotropic hypogonadism revisited.
Fraietta R, Zylberstejn DS, Esteves SC. Fraietta R, et al. Clinics (Sao Paulo). 2013;68 Suppl 1(Suppl 1):81-8. doi: 10.6061/clinics/2013(sup01)09. Clinics (Sao Paulo). 2013. PMID: 23503957 Free PMC article. Review.
., hypogonadism, can result from a primary testicular disorder (hypergonadotropic) or occur secondary to hypothalamic-pituitary dysfunction (hypogonadotropic). Hypogonadotropic hypogonadism can be congenital or acquired. Congenital hypogonadotropic hypogon
., hypogonadism, can result from a primary testicular disorder (hypergonadotropic) or occur secondary to hypothalamic-pituitary dysfunction …
Constitutional delay of puberty versus congenital hypogonadotropic hypogonadism: Genetics, management and updates.
Raivio T, Miettinen PJ. Raivio T, et al. Best Pract Res Clin Endocrinol Metab. 2019 Jun;33(3):101316. doi: 10.1016/j.beem.2019.101316. Epub 2019 Sep 5. Best Pract Res Clin Endocrinol Metab. 2019. PMID: 31522908 Free article. Review.
However, some CDGP patients may benefit from medical intervention with low-dose sex steroids or peroral aromatase inhibitor letrozole (only for boys). Other causes of DP include permanent hypogonadotropic hypogonadism, functional hypogonadotropic hypogonad
However, some CDGP patients may benefit from medical intervention with low-dose sex steroids or peroral aromatase inhibitor letrozole (only …
Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.
Boehm U, Bouloux PM, Dattani MT, de Roux N, Dodé C, Dunkel L, Dwyer AA, Giacobini P, Hardelin JP, Juul A, Maghnie M, Pitteloud N, Prevot V, Raivio T, Tena-Sempere M, Quinton R, Young J. Boehm U, et al. Nat Rev Endocrinol. 2015 Sep;11(9):547-64. doi: 10.1038/nrendo.2015.112. Epub 2015 Jul 21. Nat Rev Endocrinol. 2015. PMID: 26194704 Review.
Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder caused by the deficient production, secretion or action of gonadotropin-releasing hormone (GnRH), which is the master hormone regulating the reproductive axis. ...
Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder caused by the deficient production, secretion or action of g …
Current clinical management of constitutional delay of growth and puberty.
Gaudino R, De Filippo G, Bozzola E, Gasparri M, Bozzola M, Villani A, Radetti G. Gaudino R, et al. Ital J Pediatr. 2022 Mar 24;48(1):45. doi: 10.1186/s13052-022-01242-5. Ital J Pediatr. 2022. PMID: 35331309 Free PMC article. Review.
In details, pediatricians often cannot differentiate CDGP from permanent hypogonadotropic hypogonadism (PHH), with definitive diagnosis of PHH awaiting lack of puberty by age 18 yr. ...Patients with transient delay in hypothalamic-pituitary-gonadal axis maturation d …
In details, pediatricians often cannot differentiate CDGP from permanent hypogonadotropic hypogonadism (PHH), with definitive …
845 results