Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1963 8
1964 17
1965 4
1966 5
1967 15
1968 14
1969 23
1970 21
1971 13
1972 20
1973 18
1974 15
1975 19
1976 19
1977 11
1978 9
1979 20
1980 12
1981 14
1982 14
1983 17
1984 20
1985 26
1986 11
1987 22
1988 29
1989 22
1990 35
1991 30
1992 31
1993 57
1994 31
1995 49
1996 31
1997 51
1998 47
1999 49
2000 70
2001 76
2002 79
2003 109
2004 119
2005 133
2006 145
2007 131
2008 141
2009 133
2010 158
2011 142
2012 138
2013 150
2014 174
2015 147
2016 170
2017 138
2018 146
2019 137
2020 179
2021 162
2022 191
2023 122
2024 24

Text availability

Article attribute

Article type

Publication date

Search Results

3,842 results

Results by year

Filters applied: . Clear all
Page 1
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
Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism.
Bonomi M, Rochira V, Pasquali D, Balercia G, Jannini EA, Ferlin A; Klinefelter ItaliaN Group (KING). Bonomi M, et al. J Endocrinol Invest. 2017 Feb;40(2):123-134. doi: 10.1007/s40618-016-0541-6. Epub 2016 Sep 19. J Endocrinol Invest. 2017. PMID: 27644703 Free PMC article. Review.
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.
SETTING: Not applicable. PATIENT(S): Men seeking treatment for symptomatic hypogonadism who have used nonprescribed AAS. INTERVENTION(S): History and physical examination followed by medical intervention if necessary. MAIN OUTCOME MEASURES(S): Serum testosterone and gonado …
SETTING: Not applicable. PATIENT(S): Men seeking treatment for symptomatic hypogonadism who have used nonprescribed AAS. INTERVENTION …
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 …
Approach to the Patient With Prolactinoma.
Auriemma RS, Pirchio R, Pivonello C, Garifalos F, Colao A, Pivonello R. Auriemma RS, et al. J Clin Endocrinol Metab. 2023 Aug 18;108(9):2400-2423. doi: 10.1210/clinem/dgad174. J Clin Endocrinol Metab. 2023. PMID: 36974474 Free PMC article. Review.
Prolactinomas are the most common pituitary tumor histotype, with microprolactinomas being prevalent in women and macroprolactinomas in men. Hyperprolactinemia is among the most common causes of hypogonadotropic hypogonadism in both sexes, prompting medical advice f …
Prolactinomas are the most common pituitary tumor histotype, with microprolactinomas being prevalent in women and macroprolactinomas in men. …
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.
Primary hypogonadism is caused by gonadal (testicular or ovarian) failure. Secondary hypogonadism is the result of a dysfunction within the hypothalamus and/or pituitary. ...Hormone replacement is the hallmark of hypogonadism treatment. Restoring and/or maint …
Primary hypogonadism is caused by gonadal (testicular or ovarian) failure. Secondary hypogonadism is the result of a dysfuncti …
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 constitutio …
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.
Hypogonadotropic hypogonadism can be congenital or acquired. Congenital hypogonadotropic hypogonadism is divided into anosmic hypogonadotropic hypogonadism (Kallmann syndrome) and congenital normosmic isolated hypogonadotropic h
Hypogonadotropic hypogonadism can be congenital or acquired. Congenital hypogonadotropic hypogonadism is divided
Male Hypogonadism and Disorders of Sex Development.
Grinspon RP, Bergadá I, Rey RA. Grinspon RP, et al. Front Endocrinol (Lausanne). 2020 Apr 15;11:211. doi: 10.3389/fendo.2020.00211. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32351452 Free PMC article. Review.
In XY individuals, the process of fetal sex differentiation can be disrupted at the stage of gonadal differentiation, resulting in gonadal dysgenesis, a form of early fetal-onset primary hypogonadism characterized by insufficient androgen and anti-Mullerian hormone (AMH) p …
In XY individuals, the process of fetal sex differentiation can be disrupted at the stage of gonadal differentiation, resulting in gonadal d …
Adipose Tissue Dysfunction and Obesity-Related Male Hypogonadism.
Genchi VA, Rossi E, Lauriola C, D'Oria R, Palma G, Borrelli A, Caccioppoli C, Giorgino F, Cignarelli A. Genchi VA, et al. Int J Mol Sci. 2022 Jul 25;23(15):8194. doi: 10.3390/ijms23158194. Int J Mol Sci. 2022. PMID: 35897769 Free PMC article. Review.
In addition, androgen deficiency could further accelerate adipose tissue expansion and therefore exacerbate obesity, which in turn enhances hypogonadism, thus inducing a vicious cycle. Based on these considerations, we propose an overview on the relationship of adipose tis …
In addition, androgen deficiency could further accelerate adipose tissue expansion and therefore exacerbate obesity, which in turn enhances …
3,842 results