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1965
2025

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

Year Number of Results
1965 1
1966 4
1967 3
1968 11
1969 18
1970 6
1971 9
1972 20
1973 16
1974 23
1975 20
1976 13
1977 16
1978 24
1979 17
1980 12
1981 23
1982 23
1983 27
1984 21
1985 23
1986 19
1987 44
1988 68
1989 50
1990 68
1991 62
1992 67
1993 90
1994 93
1995 87
1996 90
1997 99
1998 108
1999 89
2000 101
2001 108
2002 97
2003 111
2004 134
2005 137
2006 143
2007 135
2008 153
2009 120
2010 135
2011 135
2012 159
2013 137
2014 155
2015 148
2016 144
2017 131
2018 106
2019 109
2020 128
2021 106
2022 81
2023 89
2024 100
2025 5

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4,145 results

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Page 1
The Reproductive System.
Pask A. Pask A. Adv Exp Med Biol. 2016;886:1-12. doi: 10.1007/978-94-017-7417-8_1. Adv Exp Med Biol. 2016. PMID: 26659484 Review.
Given the pivotal importance of correct reproductive function, it is confounding that disorders of sex development (DSDs) are among the most common congenital abnormalities in humans (Lee et al. ...This chapter provides an overview of our understanding of uro …
Given the pivotal importance of correct reproductive function, it is confounding that disorders of sex development (DSDs) are among t …
Diagnosis and treatment of müllerian malformations.
Passos IMPE, Britto RL. Passos IMPE, et al. Taiwan J Obstet Gynecol. 2020 Mar;59(2):183-188. doi: 10.1016/j.tjog.2020.01.003. Taiwan J Obstet Gynecol. 2020. PMID: 32127135 Free article. Review.
Anomalies in the mullerian ducts are congenital alterations with more prevalence than it is imagined, varying from 0.5 to 6.7% in the general population and up to 16.7% in women with recurrent miscarriage. ...
Anomalies in the mullerian ducts are congenital alterations with more prevalence than it is imagined, varying from 0.5 to 6.7% in the …
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update.
Herlin MK, Petersen MB, Brännström M. Herlin MK, et al. Orphanet J Rare Dis. 2020 Aug 20;15(1):214. doi: 10.1186/s13023-020-01491-9. Orphanet J Rare Dis. 2020. PMID: 32819397 Free PMC article. Review.
BACKGROUND: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, also referred to as Mullerian aplasia, is a congenital disorder characterized by aplasia of the uterus and upper part of the vagina in females with normal secondary sex characteristics and a normal female karyotyp …
BACKGROUND: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, also referred to as Mullerian aplasia, is a congenital disorder character …
Update on Mayer-Rokitansky-Küster-Hauser syndrome.
Chen N, Song S, Bao X, Zhu L. Chen N, et al. Front Med. 2022 Dec;16(6):859-872. doi: 10.1007/s11684-022-0969-3. Epub 2022 Dec 23. Front Med. 2022. PMID: 36562950 Review.
This review presents an update of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome on its etiologic, clinical, diagnostic, psychological, therapeutic, and reproductive aspects. The etiology of MRKH syndrome remains unclear due to its intrinsic heterogeneity. ...
This review presents an update of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome on its etiologic, clinical, diagnostic, psychological, ther …
Hypospadias, all there is to know.
van der Horst HJ, de Wall LL. van der Horst HJ, et al. Eur J Pediatr. 2017 Apr;176(4):435-441. doi: 10.1007/s00431-017-2864-5. Epub 2017 Feb 11. Eur J Pediatr. 2017. PMID: 28190103 Free PMC article. Review.
Hypospadias is one of the most common congenital anomalies in men. The condition is typically characterized by proximal displacement of the urethral opening, penile curvature, and a ventrally deficient hooded foreskin. ...
Hypospadias is one of the most common congenital anomalies in men. The condition is typically characterized by proximal displacement …
Uterine factors in recurrent pregnancy losses.
Carbonnel M, Pirtea P, de Ziegler D, Ayoubi JM. Carbonnel M, et al. Fertil Steril. 2021 Mar;115(3):538-545. doi: 10.1016/j.fertnstert.2020.12.003. Fertil Steril. 2021. PMID: 33712099 Free article. Review.
Congenital and acquired uterine anomalies are associated with recurrent pregnancy loss (RPL). Relevant congenital Mullerian tract anomalies include unicornuate, bicornuate septate, and arcuate uterus. ...
Congenital and acquired uterine anomalies are associated with recurrent pregnancy loss (RPL). Relevant congenital Mullerian tr
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implications.
Herlin MK. Herlin MK. Front Endocrinol (Lausanne). 2024 Apr 18;15:1368990. doi: 10.3389/fendo.2024.1368990. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 38699388 Free PMC article. Review.
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital anomaly characterized by agenesis/aplasia of the uterus and upper part of the vagina in females with normal external genitalia and a normal female karyotype (46,XX). ...
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital anomaly characterized by agenesis/aplasia of the uterus and upper part …
Müllerian anomalies.
Gell JS. Gell JS. Semin Reprod Med. 2003 Nov;21(4):375-88. doi: 10.1055/s-2004-815593. Semin Reprod Med. 2003. PMID: 14724770 Review.
The reproductive organs in both males and females consist of gonads, internal ductal structures, and external genitalia. ...This chapter serves to review the embryology and development of the reproductive system and to describe common genital tract ano …
The reproductive organs in both males and females consist of gonads, internal ductal structures, and external genitalia. ...Th …
Non-obstructive müllerian anomalies.
Dietrich JE, Millar DM, Quint EH. Dietrich JE, et al. J Pediatr Adolesc Gynecol. 2014 Dec;27(6):386-95. doi: 10.1016/j.jpag.2014.07.001. Epub 2014 Jul 17. J Pediatr Adolesc Gynecol. 2014. PMID: 25438707 Review.
BACKGROUND: The nonobstructive group of anatomic variants involving the reproductive tract includes vaginal agenesis as well as the congenital anomalies of the vagina and uterus, occurring without pain during the pubertal years. OBJECTIVE: The objective is to discus …
BACKGROUND: The nonobstructive group of anatomic variants involving the reproductive tract includes vaginal agenesis as well as the …
Uterine Arteriovenous Malformations.
Giurazza F, Corvino F, Silvestre M, Cavaglià E, Amodio F, Cangiano G, De Magistris G, Niola R. Giurazza F, et al. Semin Ultrasound CT MR. 2021 Feb;42(1):37-45. doi: 10.1053/j.sult.2020.08.002. Epub 2020 Aug 21. Semin Ultrasound CT MR. 2021. PMID: 33541588 Review.
The typical patient affected is a multiparous woman during her thirties. The origin can be congenital or acquired, with the latter being more common after uterine surgery and presenting mainly as arteriovenous fistulous connections into the myometrium supplied by uterine a …
The typical patient affected is a multiparous woman during her thirties. The origin can be congenital or acquired, with the latter be …
4,145 results