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1963
2025

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

Year Number of Results
1963 3
1964 2
1965 1
1966 3
1967 2
1968 11
1969 15
1970 5
1971 10
1972 16
1973 14
1974 23
1975 20
1976 10
1977 10
1978 14
1979 21
1980 12
1981 18
1982 22
1983 21
1984 22
1985 18
1986 11
1987 26
1988 37
1989 30
1990 41
1991 44
1992 49
1993 59
1994 63
1995 63
1996 54
1997 71
1998 71
1999 69
2000 77
2001 77
2002 76
2003 88
2004 104
2005 80
2006 102
2007 95
2008 118
2009 84
2010 108
2011 111
2012 109
2013 113
2014 120
2015 101
2016 110
2017 116
2018 102
2019 104
2020 118
2021 139
2022 115
2023 133
2024 99
2025 10

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3,290 results

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Page 1
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 …
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. J Pediatr Urol 8(6):611-615, 2012). Urogenital development is a highly …
Given the pivotal importance of correct reproductive function, it is confounding that disorders of sex development (DSDs) are among the most …
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
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 k …
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.
Fraser syndrome.
Chattopadhyay A, Kher AS, Udwadia AD, Sharma SV, Bharucha BA, Nicholson AD. Chattopadhyay A, et al. J Postgrad Med. 1993 Oct-Dec;39(4):228-30. J Postgrad Med. 1993. PMID: 7996504 Free article. Review.
Multiple associated anomalies were present including those of eyelids, eyebrow, face, fingers and genitalia. Chromosome analysis revealed a normal female karyotype. Pituitary gonadotropins were within normal range....
Multiple associated anomalies were present including those of eyelids, eyebrow, face, fingers and genitalia. Chromosome analysis reve …
Feminizing genitoplasty.
Hensle TW, Bingham J. Hensle TW, et al. Adv Exp Med Biol. 2002;511:251-65; discussion 265-6. doi: 10.1007/978-1-4615-0621-8_15. Adv Exp Med Biol. 2002. PMID: 12575766 Review. No abstract available.
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 …
Abnormal sex differentiation.
Saenger P. Saenger P. J Pediatr. 1984 Jan;104(1):1-17. doi: 10.1016/s0022-3476(84)80581-8. J Pediatr. 1984. PMID: 6361226 Review. No abstract available.
3,290 results