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

Year Number of Results
1965 1
1966 2
1967 4
1969 7
1970 4
1971 14
1972 10
1973 8
1974 15
1975 29
1976 37
1977 32
1978 26
1979 29
1980 28
1981 46
1982 39
1983 47
1984 58
1985 58
1986 46
1987 64
1988 63
1989 67
1990 73
1991 88
1992 90
1993 99
1994 131
1995 125
1996 141
1997 142
1998 140
1999 124
2000 162
2001 157
2002 170
2003 183
2004 186
2005 178
2006 194
2007 229
2008 213
2009 228
2010 234
2011 299
2012 323
2013 268
2014 275
2015 290
2016 285
2017 270
2018 270
2019 338
2020 324
2021 287
2022 219
2023 179
2024 98

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6,925 results

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Quoted phrase not found in phrase index: "Abnormality of reproductive system physiology"
Page 1
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 …
Uterine septum: a guideline.
Practice Committee of the American Society for Reproductive Medicine. Electronic address: ASRM@asrm.org; Practice Committee of the American Society for Reproductive Medicine. Practice Committee of the American Society for Reproductive Medicine. Electronic address: ASRM@asrm.org, et al. Fertil Steril. 2016 Sep 1;106(3):530-40. doi: 10.1016/j.fertnstert.2016.05.014. Epub 2016 May 25. Fertil Steril. 2016. PMID: 27235766 Free article. Review.
Disorders of sex development.
Witchel SF. Witchel SF. Best Pract Res Clin Obstet Gynaecol. 2018 Apr;48:90-102. doi: 10.1016/j.bpobgyn.2017.11.005. Epub 2017 Nov 22. Best Pract Res Clin Obstet Gynaecol. 2018. PMID: 29503125 Free PMC article. Review.
Disorders of sex development comprise a heterogeneous group of congenital conditions associated with atypical development of internal and external genitalia. ...Disorders of sex development can be classified into several categories including chromosomal, gonadal, an …
Disorders of sex development comprise a heterogeneous group of congenital conditions associated with atypical development of internal …
Organ Abnormalities Caused by Turner Syndrome.
Yoon SH, Kim GY, Choi GT, Do JT. Yoon SH, et al. Cells. 2023 May 11;12(10):1365. doi: 10.3390/cells12101365. Cells. 2023. PMID: 37408200 Free PMC article. Review.
Turner syndrome (TS), a genetic disorder due to incomplete dosage compensation of X-linked genes, affects multiple organ systems, leading to hypogonadotropic hypogonadism, short stature, cardiovascular and vascular abnormalities, liver disease, renal abnormalities, …
Turner syndrome (TS), a genetic disorder due to incomplete dosage compensation of X-linked genes, affects multiple organ systems, leading to …
Mechanisms of oocyte aneuploidy associated with advanced maternal age.
Mikwar M, MacFarlane AJ, Marchetti F. Mikwar M, et al. Mutat Res Rev Mutat Res. 2020 Jul-Sep;785:108320. doi: 10.1016/j.mrrev.2020.108320. Epub 2020 Jul 4. Mutat Res Rev Mutat Res. 2020. PMID: 32800274 Review.
As females advance in age, they are at higher risk of infertility, miscarriage, or having a pregnancy affected by congenital birth defects such as Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Turner syndrome (monosomy X). ...A better understanding of the …
As females advance in age, they are at higher risk of infertility, miscarriage, or having a pregnancy affected by congenital birth de …
Environmental and individual exposure and the risk of congenital anomalies: a review of recent epidemiological evidence.
Baldacci S, Gorini F, Santoro M, Pierini A, Minichilli F, Bianchi F. Baldacci S, et al. Epidemiol Prev. 2018 May-Aug;42(3-4 Suppl 1):1-34. doi: 10.19191/EP18.3-4.S1.P001.057. Epidemiol Prev. 2018. PMID: 30066535 Free article. Review. English.
INTRODUCTION: Congenital anomalies (CAs) represent one of the main cause of foetal death, infant mortality and morbidity, and long-term disability. ...In Europe, CAs are the leading cause of perinatal mortality: the European Surveillance of Congenital Anomalies (EUR …
INTRODUCTION: Congenital anomalies (CAs) represent one of the main cause of foetal death, infant mortality and morbidity, and long-te …
Congenital Uterine Malformation by Experts (CUME): better criteria for distinguishing between normal/arcuate and septate uterus?
Ludwin A, Martins WP, Nastri CO, Ludwin I, Coelho Neto MA, Leitão VM, Acién M, Alcazar JL, Benacerraf B, Condous G, De Wilde RL, Emanuel MH, Gibbons W, Guerriero S, Hurd WW, Levine D, Lindheim S, Pellicer A, Petraglia F, Saridogan E. Ludwin A, et al. Ultrasound Obstet Gynecol. 2018 Jan;51(1):101-109. doi: 10.1002/uog.18923. Ultrasound Obstet Gynecol. 2018. PMID: 29024135 Free article.
Another aim was to determine the interobserver reliability and diagnostic test accuracy of three measurements suggested by recent guidelines, using as reference standard the decision made most often by experts (Congenital Uterine Malformation by Experts (CUME)). METHODS: I …
Another aim was to determine the interobserver reliability and diagnostic test accuracy of three measurements suggested by recent guidelines …
Acro-cardio-facial syndrome.
Digilio MC, Dallapiccola B. Digilio MC, et al. Orphanet J Rare Dis. 2010 Sep 29;5:25. doi: 10.1186/1750-1172-5-25. Orphanet J Rare Dis. 2010. PMID: 20920258 Free PMC article. Review.
Acro-cardio-facial syndrome (ACFS) is a rare genetic disorder characterized by split-hand/split-foot malformation (SHFM), facial anomalies, cleft lip/palate, congenital heart defect (CHD), genital anomalies, and mental retardation. ...
Acro-cardio-facial syndrome (ACFS) is a rare genetic disorder characterized by split-hand/split-foot malformation (SHFM), facial anomalies, …
Etiologies of uterine malformations.
Jacquinet A, Millar D, Lehman A. Jacquinet A, et al. Am J Med Genet A. 2016 Aug;170(8):2141-72. doi: 10.1002/ajmg.a.37775. Epub 2016 Jun 8. Am J Med Genet A. 2016. PMID: 27273803 Review.
Sequencing of candidate genes in series of individuals with isolated uterine abnormalities has been able to suggest an association for several genes, but confirmation of a strong causative effect is still lacking for the majority of them. ...
Sequencing of candidate genes in series of individuals with isolated uterine abnormalities has been able to suggest an association fo …
Maldescendus testis.
Toppari J, Kaleva M. Toppari J, et al. Horm Res. 1999 Dec;51(6):261-9. doi: 10.1159/000023412. Horm Res. 1999. PMID: 10640886 Review.
Maldescendus testis is a common congenital abnormality occurring in 2-5% of full-term boys at birth in the Western countries. ...The etiology of the disorder is not known, but normal hypothalamo-pituitary-gonadal axis is usually a prerequisite for normal descent of …
Maldescendus testis is a common congenital abnormality occurring in 2-5% of full-term boys at birth in the Western countries. …
6,925 results