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

Year Number of Results
1974 1
1977 1
1979 1
1981 1
1982 1
1983 2
1984 4
1985 2
1986 2
1987 3
1988 5
1989 5
1990 3
1991 2
1992 3
1993 4
1994 1
1997 3
1998 2
1999 4
2000 1
2001 1
2002 1
2003 4
2004 4
2005 4
2006 10
2007 9
2008 5
2009 3
2010 13
2011 8
2012 8
2013 11
2014 13
2015 10
2016 8
2017 9
2018 4
2019 8
2020 15
2021 15
2022 8
2023 8
2024 1

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210 results

Results by year

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Page 1
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.
Congenital hypogonadotropic hypogonadism is divided into anosmic hypogonadotropic hypogonadism (Kallmann syndrome) and congenital normosmic isolated hypogonadotropic hypogonadism (idiopathic hypogonadotropic hypogonadism). ...
Congenital hypogonadotropic hypogonadism is divided into anosmic hypogonadotropic hypogonadism (Kallmann syndrome) and congenital normosmic …
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.
Isolated hypogonadotropic hypogonadism in adolescence: Do we need to measure the pituitary, stalk or other imaging markers? A retrospective magnetic resonance imaging study.
Ayaz E, Yıldırım R, Çelebi C, Özalkak Ş. Ayaz E, et al. Turk J Pediatr. 2023;65(3):445-455. doi: 10.24953/turkjped.2022.1095. Turk J Pediatr. 2023. PMID: 37395964 Free article.
Our aim was to compare the size of the pituitary gland, stalk and other previously described imaging tools in patients with isolated hypogonadotropic hypogonadism (HH) versus adolescents with a normal pituitary gland. ...
Our aim was to compare the size of the pituitary gland, stalk and other previously described imaging tools in patients with isolated
[Isolated hypogonadotropic hypogonadism].
Shozu M. Shozu M. Nihon Rinsho. 2006 Apr;64 Suppl 4:202-6. Nihon Rinsho. 2006. PMID: 16689309 Review. Japanese. No abstract available.
Molecular genetics of isolated hypogonadotropic hypogonadism and Kallmann syndrome.
Karges B, Roux N. Karges B, et al. Endocr Dev. 2005;8:67-80. doi: 10.1159/000084094. Endocr Dev. 2005. PMID: 15722618 Review.
Isolated hypogonadotropic hypogonadism (IHH) is characterized by complete or partial failure of pubertal development due to impaired secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH). ...
Isolated hypogonadotropic hypogonadism (IHH) is characterized by complete or partial failure of pubertal development du
New insights in the genetics of isolated hypogonadotropic hypogonadism.
Iovane A, Aumas C, de Roux N. Iovane A, et al. Eur J Endocrinol. 2004 Nov;151 Suppl 3:U83-8. doi: 10.1530/eje.0.151u083. Eur J Endocrinol. 2004. PMID: 15554891 Review.
Isolated gonadotropic deficiency or isolated hypogonadotropic hypogonadism is defined as a low sexual hormone secretion by the gonads associated with low LH and FSH plasma levels. ...
Isolated gonadotropic deficiency or isolated hypogonadotropic hypogonadism is defined as a low sexual hormone secretion …
A female with isolated hypogonadotropic hypogonadism: A case report and review article.
Sugiarto AM, Soelistijo SA. Sugiarto AM, et al. Ann Med Surg (Lond). 2022 Jan 26;74:103289. doi: 10.1016/j.amsu.2022.103289. eCollection 2022 Feb. Ann Med Surg (Lond). 2022. PMID: 35145667 Free PMC article.
BACKGROUND: Isolated Hypogonadotropic Hypogonadism (IHH) is a clinical syndrome that results from gonadal failure due to abnormal pituitary gonadotropin levels, in the presence of normal baseline and reserve testing of the remaining pituitary hormones. ...
BACKGROUND: Isolated Hypogonadotropic Hypogonadism (IHH) is a clinical syndrome that results from gonadal failure due t …
210 results