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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 3
1969 8
1970 3
1971 4
1972 8
1973 4
1974 8
1975 3
1976 8
1977 5
1978 5
1979 6
1980 9
1981 2
1982 6
1983 3
1984 3
1985 1
1986 2
1987 6
1988 5
1989 1
1990 2
1991 5
1992 11
1993 19
1994 6
1995 12
1996 7
1997 8
1998 12
1999 17
2000 11
2001 19
2002 19
2003 15
2004 20
2005 20
2006 25
2007 12
2008 19
2009 13
2010 34
2011 28
2012 31
2013 21
2014 25
2015 17
2016 24
2017 24
2018 19
2019 18
2020 20
2021 21
2022 25
2023 11
2024 0

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649 results

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Page 1
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
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.
Gender assignment in infants born with a difference in sexual development (DSD) remains one of the many difficult decisions faced by the multi-disciplinary treatment team as some of these children develop gender identity disorder (GID) when they become adults. ...Th …
Gender assignment in infants born with a difference in sexual development (DSD) remains one of the many difficult decisions faced by …
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.
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 …
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.
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 …
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.
Normal male genital phenotype indicates that the boy has had functioning testis during development. Torsion of the testis can cause testicular regression but in many cases the reason for vanishing testis remains elusive. ...
Normal male genital phenotype indicates that the boy has had functioning testis during development. Torsion of the testis can cause t …
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 …
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 …
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. ...In contrast to rodents, there appears to be no obvious role for estrogens in masculinizing the human brain. Furthermore, data from CAIS also suggest a contribution of sex chromos …
Widespread sex differences in human brain structure and function have been reported. ...In contrast to rodents, there appears to be n …
649 results