Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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 10
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 21
2002 25
2003 17
2004 26
2005 25
2006 30
2007 13
2008 23
2009 15
2010 39
2011 30
2012 32
2013 22
2014 28
2015 19
2016 26
2017 25
2018 19
2019 19
2020 20
2021 23
2022 26
2023 15
2024 3

Text availability

Article attribute

Article type

Publication date

Search Results

774 results

Results by year

Filters applied: . Clear all
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 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
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.
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 …
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 …
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 …
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 …
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 …
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 …
Genetic control of typical and atypical sex development.
Reyes AP, León NY, Frost ER, Harley VR. Reyes AP, et al. Nat Rev Urol. 2023 Jul;20(7):434-451. doi: 10.1038/s41585-023-00754-x. Epub 2023 Apr 5. Nat Rev Urol. 2023. PMID: 37020056 Review.
Differences in sex development (DSD) arise from congenital alterations during any of these processes, and are classified depending on sex chromosomal constitution as sex chromosome DSD, 46,XY DSD or 46,XX DSD. Understanding the genetics a …
Differences in sex development (DSD) arise from congenital alterations during any of these processes, and are classified depen …
774 results