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

Year Number of Results
1965 1
1967 2
1968 4
1969 8
1970 3
1971 4
1972 8
1973 4
1974 9
1975 3
1976 8
1977 6
1978 5
1979 6
1980 12
1981 2
1982 6
1983 4
1984 3
1985 1
1986 3
1987 9
1988 6
1989 4
1990 4
1991 8
1992 18
1993 30
1994 10
1995 18
1996 10
1997 11
1998 16
1999 21
2000 14
2001 20
2002 25
2003 17
2004 26
2005 25
2006 29
2007 13
2008 22
2009 14
2010 37
2011 29
2012 31
2013 21
2014 26
2015 18
2016 24
2017 25
2018 19
2019 19
2020 20
2021 22
2022 25
2023 12
2024 0

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752 results

Results by year

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Page 1
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.
Genetics of cryptorchidism and testicular regression.
Elamo HP, Virtanen HE, Toppari J. Elamo HP, et al. Best Pract Res Clin Endocrinol Metab. 2022 Jan;36(1):101619. doi: 10.1016/j.beem.2022.101619. Epub 2022 Feb 4. Best Pract Res Clin Endocrinol Metab. 2022. PMID: 35193821 Free article. Review.
., undescended testis, is one of the most common genital malformations in newborn male babies. The birth rate of cryptorchidism varies from 1.6 to 9.0 %. ...Testicular regression can also cause an empty scrotum. Normal male genital phenotype indicates that the boy h …
., undescended testis, is one of the most common genital malformations in newborn male babies. The birth rate of cryptorchidism varie …
Androgen insensitivity syndrome: a review.
Batista RL, Costa EMF, Rodrigues AS, Gomes NL, Faria JA Jr, Nishi MY, Arnhold IJP, Domenice S, Mendonca BB. Batista RL, et al. Arch Endocrinol Metab. 2018 Mar-Apr;62(2):227-235. doi: 10.20945/2359-3997000000031. Arch Endocrinol Metab. 2018. PMID: 29768628 Free PMC article. Review.
Androgenic insensitivity syndrome is the most common cause of disorders of sexual differentiation in 46,XY individuals. It results from alterations in the androgen receptor gene, leading to a frame of hormonal resistance, which may present clinically under 3 phenoty …
Androgenic insensitivity syndrome is the most common cause of disorders of sexual differentiation in 46,XY individuals. It res …
Genetics of 46,XY gonadal dysgenesis.
Elzaiat M, McElreavey K, Bashamboo A. Elzaiat M, et al. Best Pract Res Clin Endocrinol Metab. 2022 Jan;36(1):101633. doi: 10.1016/j.beem.2022.101633. Epub 2022 Feb 25. Best Pract Res Clin Endocrinol Metab. 2022. PMID: 35249806 Review.
In 46,XY men, testis is determined by a genetic network(s) that both promotes testis formation and represses ovarian development. Disruption of this process results in a lack of testis-determination and affected individuals present with 46,XY go …
In 46,XY men, testis is determined by a genetic network(s) that both promotes testis formation and represses ovarian develo
Androgen insensitivity syndrome.
Gulía C, Baldassarra S, Zangari A, Briganti V, Gigli S, Gaffi M, Signore F, Vallone C, Nucciotti R, Costantini FM, Pizzuti A, Bernardo S, Porrello A, Piergentili R. Gulía C, et al. Eur Rev Med Pharmacol Sci. 2018 Jun;22(12):3873-3887. doi: 10.26355/eurrev_201806_15272. Eur Rev Med Pharmacol Sci. 2018. PMID: 29949163 Free article. Review.
MATERIALS AND METHODS: We searched PubMed with a larger emphasis on the physiology, genetics and current management of AIS. RESULTS: AIS is an X-linked recessive Disorder of Sex Development (DSD). It is caused by mutations of the Androgen Receptor, and their …
MATERIALS AND METHODS: We searched PubMed with a larger emphasis on the physiology, genetics and current management of AIS. RESULTS: AIS is …
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.
Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency (IGD) IGD is a genetically and clinically heterogeneous disorder. Mutations in many different genes are able to explain ~40% of the causes of IGD, with the rest of cases remaining genetically uncharacterized. ...The …
Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency (IGD) IGD is a genetically and clinically heterogeneous disorder. Mutations …
Androgen insensitivity syndrome.
Hughes IA, Davies JD, Bunch TI, Pasterski V, Mastroyannopoulou K, MacDougall J. Hughes IA, et al. Lancet. 2012 Oct 20;380(9851):1419-28. doi: 10.1016/S0140-6736(12)60071-3. Epub 2012 Jun 13. Lancet. 2012. PMID: 22698698 Free article. Review.
Androgen insensitivity syndrome in its complete form is a disorder of hormone resistance characterised by a female phenotype in an individual with an XY karyotype and testes producing age-appropriate normal concentrations of androgens. ...Management of androgen insensitivi …
Androgen insensitivity syndrome in its complete form is a disorder of hormone resistance characterised by a female phenotype in an in …
The role of steroid hormones in the sexual differentiation of the human brain.
Bakker J. Bakker J. J Neuroendocrinol. 2022 Feb;34(2):e13050. doi: 10.1111/jne.13050. Epub 2021 Oct 27. J Neuroendocrinol. 2022. PMID: 34708466 Free article. Review.
Widespread sex differences in human brain structure and function have been reported. ...It was shown that typical male neural and behavioral characteristics develop under the influence of testosterone, mostly acting during perinatal development. ...
Widespread sex differences in human brain structure and function have been reported. ...It was shown that typical male neural …
Gender identity disorder (GID) in adolescents and adults with differences of sex development (DSD): A systematic review and meta-analysis.
Babu R, Shah U. Babu R, et al. J Pediatr Urol. 2021 Feb;17(1):39-47. doi: 10.1016/j.jpurol.2020.11.017. Epub 2020 Nov 12. J Pediatr Urol. 2021. PMID: 33246831 Review.
The secondary outcome of this review is to help physicians in appropriate sex assignment of DSD children so that development of GID in later life can be reduced. ...CONCLUSIONS: GID is low in women with CAH, CAIS and CGD favoring female sex of rearing in thes …
The secondary outcome of this review is to help physicians in appropriate sex assignment of DSD children so that development o …
Androgen insensitivity syndrome: a review.
Delli Paoli E, Di Chiano S, Paoli D, Lenzi A, Lombardo F, Pallotti F. Delli Paoli E, et al. J Endocrinol Invest. 2023 Nov;46(11):2237-2245. doi: 10.1007/s40618-023-02127-y. Epub 2023 Jun 10. J Endocrinol Invest. 2023. PMID: 37300628 Review.
PURPOSE: Androgen insensitivity syndrome (AIS) is a disorder characterized by peripheral androgen resistance due to androgen receptor mutations in subjects with 46 XY karyotype. ...RESULTS: AIS is determined by a large variety of X-linked mutations that accou …
PURPOSE: Androgen insensitivity syndrome (AIS) is a disorder characterized by peripheral androgen resistance due to androgen receptor …
752 results