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

Year Number of Results
1985 1
1993 1
2004 2
2005 1
2006 4
2007 4
2008 1
2009 2
2010 6
2011 3
2012 2
2013 1
2014 3
2015 3
2016 2
2017 1
2019 1
2020 2
2021 2
2022 1
2024 0

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9 results

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Filters applied: Meta-Analysis, Review, Systematic Review, in the last 10 years. Clear all
Page 1
Molecular and Genetic Aspects of Congenital Isolated Hypogonadotropic Hypogonadism.
Lima Amato LG, Latronico AC, Gontijo Silveira LF. Lima Amato LG, et al. Endocrinol Metab Clin North Am. 2017 Jun;46(2):283-303. doi: 10.1016/j.ecl.2017.01.010. Epub 2017 Feb 23. Endocrinol Metab Clin North Am. 2017. PMID: 28476224 Review.
Congenital isolated hypogonadotropic hypogonadism (IHH) is a clinically and genetically heterogenous disorder characterized by abnormal synthesis, secretion, or action of gonadotropin-releasing hormone, a key hypothalamic decapeptide that orchestrates the rep …
Congenital isolated hypogonadotropic hypogonadism (IHH) is a clinically and genetically heterogenous disorder character …
Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency.
Balasubramanian R, Crowley WF Jr. Balasubramanian R, et al. 2007 May 23 [updated 2022 May 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 May 23 [updated 2022 May 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301509 Free Books & Documents. Review.
Genetics of hypogonadotropic hypogonadism.
Millar AC, Faghfoury H, Bieniek JM. Millar AC, et al. Transl Androl Urol. 2021 Mar;10(3):1401-1409. doi: 10.21037/tau.2020.03.33. Transl Androl Urol. 2021. PMID: 33850776 Free PMC article. Review.
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. ...
A genetic basis of congenital isolated hypogonadotropic hypogonadism (CHH) can be defined in almost 50% of cases, albei …
Nutritional and Pubertal Disorders.
Muñoz-Calvo MT, Argente J. Muñoz-Calvo MT, et al. Endocr Dev. 2016;29:153-73. doi: 10.1159/000438884. Epub 2015 Dec 17. Endocr Dev. 2016. PMID: 26680577 Review.
Patients with anorexia nervosa (AN) exhibit multiple endocrine abnormalities, including isolated hypogonadotropic hypogonadism. The delay in pubertal development and reduction in growth seen in AN patients may be a direct result of malnutrition. ...
Patients with anorexia nervosa (AN) exhibit multiple endocrine abnormalities, including isolated hypogonadotropic hypogonad
Insights into the molecular regulatory network of pathomechanisms in osteochondroma.
Yang C, Zhang R, Lin H, Wang H. Yang C, et al. J Cell Biochem. 2019 Oct;120(10):16362-16369. doi: 10.1002/jcb.29155. Epub 2019 Jun 18. J Cell Biochem. 2019. PMID: 31211456 Review.
Accumulating evidence suggests that mutations in the EXT family induce changes in isolated hypogonadotropic hypogonadism-parathyroid hormone-related protein, bone morphogenetic protein, and fibroblast growth factor signaling pathways. ...
Accumulating evidence suggests that mutations in the EXT family induce changes in isolated hypogonadotropic hypogonadism
[Kisspeptin and leptin in the regulation of fertility].
Pankov YA. Pankov YA. Mol Biol (Mosk). 2015 Sep-Oct;49(5):707-15. doi: 10.7868/S0026898415050134. Mol Biol (Mosk). 2015. PMID: 26510589 Free article. Review. Russian.
The p.P74S, p.H90D, and p.P110T missense mutations of KISS1 are associated with central precocious puberty (CPP); and the p.G35S, p.C53R, and p.F117L mutations, with delayed puberty and isolated hypogonadotropic hypogonadism (IHH). The p.P196H and p.R386P mut …
The p.P74S, p.H90D, and p.P110T missense mutations of KISS1 are associated with central precocious puberty (CPP); and the p.G35S, p.C53R, an …
Normal Variation in Pubertal Timing: Genetic Determinants in Relation to Growth and Adiposity.
Willemsen RH, Dunger DB. Willemsen RH, et al. Endocr Dev. 2016;29:17-35. doi: 10.1159/000438957. Epub 2015 Dec 17. Endocr Dev. 2016. PMID: 26680570 Review.
Recently, a few rare genetic causes of precocious puberty have been reported as well as genetic mutations associated with isolated hypogonadotropic hypogonadism. Genome-wide association (GWA) studies have helped to explore the genetic determinants of the norm …
Recently, a few rare genetic causes of precocious puberty have been reported as well as genetic mutations associated with isolated
[Research progress of kisspeptin in female reproductive endocrine and assisted reproductive techniques].
Zhang Y, Sun NX. Zhang Y, et al. Sheng Li Xue Bao. 2020 Feb 25;72(1):125-132. Sheng Li Xue Bao. 2020. PMID: 32099990 Free article. Review. Chinese.
With the discovery that kisspeptin is involved in the pathological process of reproductive endocrine diseases such as isolated hypogonadotropic hypogonadism (IHH), polycystic ovary syndrome (PCOS), premature ovarian failure (POF) and pathological hyperprolact …
With the discovery that kisspeptin is involved in the pathological process of reproductive endocrine diseases such as isolated hyp