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

Year Number of Results
1972 1
1976 3
1978 1
1979 3
1980 1
1982 2
1983 2
1984 3
1985 2
1986 2
1987 1
1988 1
1989 1
1990 4
1991 5
1992 3
1993 2
1994 3
1995 4
1996 1
1997 6
1998 3
1999 1
2000 1
2001 4
2002 5
2003 1
2004 6
2005 1
2006 4
2007 9
2008 6
2009 7
2010 9
2011 5
2012 6
2013 7
2014 10
2015 8
2016 6
2017 11
2018 6
2019 14
2020 5
2021 8
2022 9
2023 6
2024 5

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196 results

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Page 1
Diagnosis of fetal non-chromosomal abnormalities on routine ultrasound examination at 11-13 weeks' gestation.
Syngelaki A, Hammami A, Bower S, Zidere V, Akolekar R, Nicolaides KH. Syngelaki A, et al. Ultrasound Obstet Gynecol. 2019 Oct;54(4):468-476. doi: 10.1002/uog.20844. Ultrasound Obstet Gynecol. 2019. PMID: 31408229 Free article.

Common abnormalities that were detected in < 10% of cases at 11-13 weeks included ventriculomegaly, agenesis of the corpus callosum, isolated cleft lip, congenital pulmonary airway malformation, ventricular septal defect, abdominal cysts, unilateral renal agen

…

Common abnormalities that were detected in < 10% of cases at 11-13 weeks included ventriculomegaly, agenesis of the corpus callosum, isol

…
Unilateral renal agenesis: a systematic review on associated anomalies and renal injury.
Westland R, Schreuder MF, Ket JC, van Wijk JA. Westland R, et al. Nephrol Dial Transplant. 2013 Jul;28(7):1844-55. doi: 10.1093/ndt/gft012. Epub 2013 Feb 28. Nephrol Dial Transplant. 2013. PMID: 23449343 Review.
BACKGROUND: Unilateral renal agenesis (URA) is associated with other congenital anomalies of the kidney and urinary tract (CAKUT) and extra-renal anomalies. ...
BACKGROUND: Unilateral renal agenesis (URA) is associated with other congenital anomalies of the kidney and urinary tra …
Unilateral renal agenesis.
Robson WL, Leung AK, Rogers RC. Robson WL, et al. Adv Pediatr. 1995;42:575-92. Adv Pediatr. 1995. PMID: 8540439 Review.
Unilateral renal agenesis is a relatively common congenital urinary malformation that is usually diagnosed during fetal ultrasonography. Some cases of URA may represent involution of a previous MCDK. Unilateral renal agenesis may be an is …
Unilateral renal agenesis is a relatively common congenital urinary malformation that is usually diagnosed during fetal …
Advances in Genetic Diagnosis of Kallmann Syndrome and Genetic Interruption.
Liu Y, Zhi X. Liu Y, et al. Reprod Sci. 2022 Jun;29(6):1697-1709. doi: 10.1007/s43032-021-00638-8. Epub 2021 Jul 6. Reprod Sci. 2022. PMID: 34231173 Free PMC article. Review.
Besides, mirror movements, dental agenesis, digital bone abnormalities, unilateral renal agenesis, midline facial defects, hearing loss, and eye movement abnormalities can also be observed in KS patients. ...
Besides, mirror movements, dental agenesis, digital bone abnormalities, unilateral renal agenesis, midline facial defec …
Retrospective evaluation of children with unilateral renal agenesis.
Güngör T, Yazılıtaş F, Çakıcı EK, Ekşioğlu AS, Çelikkaya E, Karakaya D, Bağlan E, Bülbül M. Güngör T, et al. Pediatr Nephrol. 2021 Sep;36(9):2847-2855. doi: 10.1007/s00467-021-05027-6. Epub 2021 Mar 16. Pediatr Nephrol. 2021. PMID: 33723672
BACKGROUND: Children born with unilateral renal agenesis (URA) are thought to have a risk of developing hypertension, proteinuria, and progressive chronic kidney disease (CKD). ...
BACKGROUND: Children born with unilateral renal agenesis (URA) are thought to have a risk of developing hypertension, p …
Mayer-Rokitansky-Küster-Hauser syndrome as an interdisciplinary problem.
Liszewska-Kapłon M, Strózik M, Kotarski Ł, Bagłaj M, Hirnle L. Liszewska-Kapłon M, et al. Adv Clin Exp Med. 2020 Apr;29(4):505-511. doi: 10.17219/acem/118850. Adv Clin Exp Med. 2020. PMID: 32348039 Free article. Review.
We can distinguish 2 types of the MRKH syndrome: type I, which is characterized by an isolated absence of 2/3 of the vagina and uterus; and type II or MURCS (Mullerian duct aplasia, unilateral renal agenesis and cervicothoracic somite anomalies), which is als …
We can distinguish 2 types of the MRKH syndrome: type I, which is characterized by an isolated absence of 2/3 of the vagina and uterus; and …
Fraser syndrome: review of the literature illustrated by a historical adult case.
Bouaoud J, Olivetto M, Testelin S, Dakpe S, Bettoni J, Devauchelle B. Bouaoud J, et al. Int J Oral Maxillofac Surg. 2020 Oct;49(10):1245-1253. doi: 10.1016/j.ijom.2020.01.007. Epub 2020 Jan 22. Int J Oral Maxillofac Surg. 2020. PMID: 31982235 Review.
Diagnosis is based on the major and minor criteria established by van Haelst et al. in 2007. Unilateral or bilateral cryptophthalmos, syndactyly, unilateral renal agenesis, and genital anomalies are the most frequent anomalies. ...
Diagnosis is based on the major and minor criteria established by van Haelst et al. in 2007. Unilateral or bilateral cryptophthalmos, syndac …
The genetic etiologies of bilateral renal agenesis.
Kirschen GW, Blakemore K, Al-Kouatly HB, Fridkis G, Baschat A, Gearhart J, Jelin AC. Kirschen GW, et al. Prenat Diagn. 2024 Feb;44(2):205-221. doi: 10.1002/pd.6516. Epub 2024 Jan 5. Prenat Diagn. 2024. PMID: 38180355 Review.
Five genes have been reported to associate with BRA without other renal anomalies; sixteen others associate with both BRA as well as unilateral renal agenesis. Six clinically recognized syndromes/associations were identified with an unknown underlying genetic …
Five genes have been reported to associate with BRA without other renal anomalies; sixteen others associate with both BRA as well as unil …
196 results