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

Year Number of Results
1934 1
1937 1
1941 1
1945 3
1946 12
1947 21
1948 11
1949 23
1950 34
1951 40
1952 41
1953 51
1954 39
1955 51
1956 50
1957 61
1958 67
1959 61
1960 68
1961 70
1962 94
1963 171
1964 217
1965 152
1966 157
1967 175
1968 193
1969 218
1970 212
1971 212
1972 209
1973 211
1974 234
1975 228
1976 199
1977 182
1978 197
1979 203
1980 168
1981 165
1982 190
1983 193
1984 199
1985 208
1986 205
1987 215
1988 212
1989 206
1990 221
1991 204
1992 199
1993 261
1994 203
1995 230
1996 212
1997 237
1998 260
1999 255
2000 302
2001 281
2002 302
2003 357
2004 401
2005 435
2006 481
2007 492
2008 531
2009 538
2010 603
2011 623
2012 630
2013 687
2014 737
2015 744
2016 759
2017 681
2018 736
2019 754
2020 891
2021 845
2022 865
2023 732
2024 749
2025 796
2026 648

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23,009 results

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Page 1
Hypogonadotropic Hypogonadism.
Bangalore Krishna K, Fuqua JS, Witchel SF. Bangalore Krishna K, et al. Endocrinol Metab Clin North Am. 2024 Jun;53(2):279-292. doi: 10.1016/j.ecl.2024.01.008. Epub 2024 Feb 19. Endocrinol Metab Clin North Am. 2024. PMID: 38677870 Review.
One cause of delayed/absent puberty is hypogonadotropic hypogonadism (HH), which refers to inadequate hypothalamic/pituitary function leading to deficient production of sex steroids in males and females. Individuals with HH typically have normal gonads, and thus HH …
One cause of delayed/absent puberty is hypogonadotropic hypogonadism (HH), which refers to inadequate hypothalamic/pituitary f …
Gonadotropin-Releasing Hormone Receptor (GnRHR) and Hypogonadotropic Hypogonadism.
Fanis P, Neocleous V, Papapetrou I, Phylactou LA, Skordis N. Fanis P, et al. Int J Mol Sci. 2023 Nov 4;24(21):15965. doi: 10.3390/ijms242115965. Int J Mol Sci. 2023. PMID: 37958948 Free PMC article. Review.
Dysregulation of the axis leads to conditions such as congenital hypogonadotropic hypogonadism (CHH) and delayed puberty. The pathophysiology of GnRHR makes it a potential target for treatments in several reproductive diseases and in congenital adrenal hyperplasia. …
Dysregulation of the axis leads to conditions such as congenital hypogonadotropic hypogonadism (CHH) and delayed puberty. The …
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 hypogonadotropic hypogonadism].
Köhn FM. Köhn FM. MMW Fortschr Med. 2023 Feb;165(Suppl 1):30-31. doi: 10.1007/s15006-023-2353-x. MMW Fortschr Med. 2023. PMID: 36849770 Review. German. No abstract available.
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
Hypogonadotropic hypogonadism as a cause of NOA and its treatment.
Salvio G, Balercia G, Kadioglu A. Salvio G, et al. Asian J Androl. 2025 May 1;27(3):322-329. doi: 10.4103/aja202483. Epub 2024 Oct 22. Asian J Androl. 2025. PMID: 39513636 Free PMC article. Review.
Hypogonadotropic hypogonadism (HH) represents a relatively rare cause of nonobstructive azoospermia (NOA), but its knowledge is crucial for the clinical andrologists, as it represents a condition that can be corrected with medical therapy in 3 quarters of cases. ...
Hypogonadotropic hypogonadism (HH) represents a relatively rare cause of nonobstructive azoospermia (NOA), but its knowledge i
Hypogonadotropic hypogonadism.
Hayes FJ, Seminara SB, Crowley WF Jr. Hayes FJ, et al. Endocrinol Metab Clin North Am. 1998 Dec;27(4):739-63, vii. doi: 10.1016/s0889-8529(05)70039-6. Endocrinol Metab Clin North Am. 1998. PMID: 9922906 Review.
This article outlines the changing pattern of gonadotropin-releasing hormone (GnRH)-induced gonadotropin secretion across sexual development, a knowledge of which is critical to understanding GnRH secretion in pathologic states such as hypogonadotropic hypogonadism. …
This article outlines the changing pattern of gonadotropin-releasing hormone (GnRH)-induced gonadotropin secretion across sexual development …
Hypogonadotropic hypogonadism.
Silveira LF, MacColl GS, Bouloux PM. Silveira LF, et al. Semin Reprod Med. 2002 Nov;20(4):327-38. doi: 10.1055/s-2002-36707. Semin Reprod Med. 2002. PMID: 12536356 Review.
Hypogonadotropic hypogonadism is characterized by failure of gonadal function secondary to deficient gonadotropin secretion, resulting from either a pituitary or hypothalamic defect, and is commonly seen in association with structural lesions or functional defects a
Hypogonadotropic hypogonadism is characterized by failure of gonadal function secondary to deficient gonadotropin secretion, r
Management of congenital hypogonadotropic hypogonadism in females.
Naseem H, Lokman M, Fitzgerald C. Naseem H, et al. Hum Fertil (Camb). 2023 Jul;26(3):622-631. doi: 10.1080/14647273.2021.1998929. Epub 2021 Nov 9. Hum Fertil (Camb). 2023. PMID: 34753367 Free article. Review.
This review explores the challenges in the diagnosis of hypogonadotropic hypogonadism, the transition of care from paediatric to adult care and the considerable health implications of this condition. ...The holistic management of women with hypogonadotropic
This review explores the challenges in the diagnosis of hypogonadotropic hypogonadism, the transition of care from paediatric …
Hypogonadotropic hypogonadism.
Layman LC. Layman LC. Endocrinol Metab Clin North Am. 2007 Jun;36(2):283-96. doi: 10.1016/j.ecl.2007.03.010. Endocrinol Metab Clin North Am. 2007. PMID: 17543719 Review.
Gonadotropin-releasing hormone (GnRH) and olfactory neurons migrate together from the olfactory placode, and GnRH neurons eventually reside in the hypothalamus. Hypogonadism in male infants may be diagnosed in the first 6 months of life but cannot be diagnosed during child …
Gonadotropin-releasing hormone (GnRH) and olfactory neurons migrate together from the olfactory placode, and GnRH neurons eventually reside …
23,009 results
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