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

Year Number of Results
1969 1
1971 1
1975 1
1976 4
1979 3
1980 2
1982 1
1983 2
1984 1
1985 3
1986 5
1987 5
1988 5
1989 5
1990 5
1991 8
1992 6
1993 3
1994 2
1995 9
1996 12
1997 6
1998 8
1999 6
2000 6
2001 4
2002 10
2003 13
2004 11
2005 11
2006 18
2007 11
2008 15
2009 17
2010 29
2011 19
2012 21
2013 22
2014 18
2015 33
2016 26
2017 24
2018 27
2019 23
2020 29
2021 42
2022 46
2023 24
2024 6

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542 results

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Page 1
Evaluation of Female Fertility-AMH and Ovarian Reserve Testing.
Cedars MI. Cedars MI. J Clin Endocrinol Metab. 2022 May 17;107(6):1510-1519. doi: 10.1210/clinem/dgac039. J Clin Endocrinol Metab. 2022. PMID: 35100616 Review.
RESULTS: Serum AMH estimates ovarian reserve, helps determine dosing in ovarian stimulation, and predicts stimulation response. As such, AMH is a good marker of oocyte quantity but does not reflect oocyte health or chances for pregnancy. ...AMH levels must be interpreted i …
RESULTS: Serum AMH estimates ovarian reserve, helps determine dosing in ovarian stimulation, and predicts stimulation response. As su …
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 …
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. ...In most cases, fertility can be induc …
Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder caused by the deficient production, secretion or action of g …
Organ Abnormalities Caused by Turner Syndrome.
Yoon SH, Kim GY, Choi GT, Do JT. Yoon SH, et al. Cells. 2023 May 11;12(10):1365. doi: 10.3390/cells12101365. Cells. 2023. PMID: 37408200 Free PMC article. Review.
Turner syndrome (TS), a genetic disorder due to incomplete dosage compensation of X-linked genes, affects multiple organ systems, leading to hypogonadotropic hypogonadism, short stature, cardiovascular and vascular abnormalities, liver disease, renal abnormalities, …
Turner syndrome (TS), a genetic disorder due to incomplete dosage compensation of X-linked genes, affects multiple organ systems, leading to …
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.
Miraoui H, Dwyer AA, Sykiotis GP, Plummer L, Chung W, Feng B, Beenken A, Clarke J, Pers TH, Dworzynski P, Keefe K, Niedziela M, Raivio T, Crowley WF Jr, Seminara SB, Quinton R, Hughes VA, Kumanov P, Young J, Yialamas MA, Hall JE, Van Vliet G, Chanoine JP, Rubenstein J, Mohammadi M, Tsai PS, Sidis Y, Lage K, Pitteloud N. Miraoui H, et al. Am J Hum Genet. 2013 May 2;92(5):725-43. doi: 10.1016/j.ajhg.2013.04.008. Am J Hum Genet. 2013. PMID: 23643382 Free PMC article.
Congenital hypogonadotropic hypogonadism (CHH) and its anosmia-associated form (Kallmann syndrome [KS]) are genetically heterogeneous. ...Except for FGF18 and SPRY2, all other genes were found to be mutated in CHH individuals: FGF17 (n = 3 individuals), IL17RD (n = …
Congenital hypogonadotropic hypogonadism (CHH) and its anosmia-associated form (Kallmann syndrome [KS]) are genetically hetero …
Management of hypogonadism from birth to adolescence.
Howard SR, Dunkel L. Howard SR, et al. Best Pract Res Clin Endocrinol Metab. 2018 Aug;32(4):355-372. doi: 10.1016/j.beem.2018.05.011. Epub 2018 Jun 6. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30086863 Review.
The main differential diagnoses of delayed puberty include self-limited delayed puberty (DP), idiopathic hypogonadotropic hypogonadism (IHH) and hypergonadotropic hypogonadism. Treatment of self-limited DP involves expectant observation or short courses of lo …
The main differential diagnoses of delayed puberty include self-limited delayed puberty (DP), idiopathic hypogonadotropic hypogona …
Obesity-Related Hypogonadism in Women.
Eng PC, Phylactou M, Qayum A, Woods C, Lee H, Aziz S, Moore B, Miras AD, Comninos AN, Tan T, Franks S, Dhillo WS, Abbara A. Eng PC, et al. Endocr Rev. 2024 Mar 4;45(2):171-189. doi: 10.1210/endrev/bnad027. Endocr Rev. 2024. PMID: 37559411 Free PMC article. Review.
Obesity-related hypogonadotropic hypogonadism is a well-characterized condition in men (termed male obesity-related secondary hypogonadism; MOSH); however, an equivalent condition has not been as clearly described in women. The prevalence of polycystic ovary syndrom …
Obesity-related hypogonadotropic hypogonadism is a well-characterized condition in men (termed male obesity-related secondary …
Hypogonadotropic Hypogonadism in Men With Diabesity.
Dhindsa S, Ghanim H, Batra M, Dandona P. Dhindsa S, et al. Diabetes Care. 2018 Jul;41(7):1516-1525. doi: 10.2337/dc17-2510. Diabetes Care. 2018. PMID: 29934480 Free PMC article. Review.
One-third of men with obesity or type 2 diabetes have subnormal free testosterone concentrations. The lower free testosterone concentrations are observed in obese men at all ages, including adolescents at completion of puberty. The gonadotropin concentrations in these male …
One-third of men with obesity or type 2 diabetes have subnormal free testosterone concentrations. The lower free testosterone concentrations …
Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease.
Cangiano B, Swee DS, Quinton R, Bonomi M. Cangiano B, et al. Hum Genet. 2021 Jan;140(1):77-111. doi: 10.1007/s00439-020-02147-1. Epub 2020 Mar 21. Hum Genet. 2021. PMID: 32200437 Review.
A genetic basis of congenital isolated hypogonadotropic hypogonadism (CHH) can be defined in almost 50% of cases, albeit not necessarily the complete genetic basis. ...Robust genotype-phenotype relationships can generally only be established for individuals who are …
A genetic basis of congenital isolated hypogonadotropic hypogonadism (CHH) can be defined in almost 50% of cases, albeit not n …
Clinical, hormonal, and genetic characteristics of 25 Chinese patients with idiopathic hypogonadotropic hypogonadism.
Liu Q, Yin X, Li P. Liu Q, et al. BMC Endocr Disord. 2022 Jan 28;22(1):30. doi: 10.1186/s12902-022-00940-9. BMC Endocr Disord. 2022. PMID: 35090434 Free PMC article.
BACKGROUND: Idiopathic hypogonadotropic hypogonadism (IHH) is a type of congenital disease caused by a variety of gene variants leading to dysfunction in the secretion of hypothalamic gonadotropin-releasing hormones (GnRHs). Clinically, IHH can be divided into Kallm …
BACKGROUND: Idiopathic hypogonadotropic hypogonadism (IHH) is a type of congenital disease caused by a variety of gene variant …
542 results