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

Year Number of Results
1974 1
1984 1
1986 2
1987 1
1988 1
1989 2
1990 1
1991 6
1992 4
1993 4
1994 3
1995 8
1996 5
1997 10
1998 6
1999 7
2000 5
2001 4
2002 8
2003 3
2004 4
2005 4
2006 8
2007 6
2008 4
2009 10
2010 8
2011 4
2012 6
2013 8
2014 16
2015 3
2016 5
2017 9
2018 9
2019 6
2020 7
2021 10
2022 7
2023 5

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201 results

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Page 1
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.
IGD is also characterized by a wide variety of non-reproductive features, including midline facial defects such as cleft lip and/or palate, renal agenesis, short metacarpals and other bone abnormalities, hearing loss, synkinesia, eye movement abnormalities, poor bal …
IGD is also characterized by a wide variety of non-reproductive features, including midline facial defects such as cleft lip and/or palate, …
Congenital Anomalies of the Upper Urinary Tract: A Comprehensive Review.
Houat AP, Guimarães CTS, Takahashi MS, Rodi GP, Gasparetto TPD, Blasbalg R, Velloni FG. Houat AP, et al. Radiographics. 2021 Mar-Apr;41(2):462-486. doi: 10.1148/rg.2021200078. Epub 2021 Jan 29. Radiographics. 2021. PMID: 33513074 Review.
Congenital anomalies of the kidneys and ureters comprise a wide spectrum of disorders ranging from simple variants with no clinical significance to complex anomalies that may lead to severe complications and end-stage renal disease. They may be classified as anomalies of …
Congenital anomalies of the kidneys and ureters comprise a wide spectrum of disorders ranging from simple variants with no clinical signific …
Life with one kidney.
Schreuder MF. Schreuder MF. Pediatr Nephrol. 2018 Apr;33(4):595-604. doi: 10.1007/s00467-017-3686-4. Epub 2017 May 29. Pediatr Nephrol. 2018. PMID: 28555299 Free PMC article. Review.
In contrast, our research group has demonstrated that being born with or acquiring a SFK in childhood results in renal injury before adulthood in over 50% of those affected. Most congenital cases will be detected during antenatal ultrasound screening, but up to 38% of case …
In contrast, our research group has demonstrated that being born with or acquiring a SFK in childhood results in renal injury before …
Renal development in the fetus and premature infant.
Rosenblum S, Pal A, Reidy K. Rosenblum S, et al. Semin Fetal Neonatal Med. 2017 Apr;22(2):58-66. doi: 10.1016/j.siny.2017.01.001. Epub 2017 Feb 1. Semin Fetal Neonatal Med. 2017. PMID: 28161315 Free PMC article. Review.
CAKUT represent a broad spectrum of abnormalities, from transient hydronephrosis to severe bilateral renal agenesis. CAKUT are a major contributor to chronic and end stage kidney disease (CKD/ESKD) in children. ...Monogenic gene mutations identified in human CAKUT h …
CAKUT represent a broad spectrum of abnormalities, from transient hydronephrosis to severe bilateral renal agenesis. CAKUT are …
Ultrasound diagnosis of fetal renal abnormalities.
Dias T, Sairam S, Kumarasiri S. Dias T, et al. Best Pract Res Clin Obstet Gynaecol. 2014 Apr;28(3):403-15. doi: 10.1016/j.bpobgyn.2014.01.009. Epub 2014 Jan 29. Best Pract Res Clin Obstet Gynaecol. 2014. PMID: 24524801 Review.
A mid-trimester anomaly scan enables detection of most renal anomalies with higher sensitivity. Bilateral renal agenesis can be confirmed ultrasonically, with empty renal fossae and absent bladder filling, along with severe oligohydramnios or anhydramn …
A mid-trimester anomaly scan enables detection of most renal anomalies with higher sensitivity. Bilateral renal agenesis …
Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology.
La Scola C, Ammenti A, Bertulli C, Bodria M, Brugnara M, Camilla R, Capone V, Casadio L, Chimenz R, Conte ML, Conversano E, Corrado C, Guarino S, Luongo I, Marsciani M, Marzuillo P, Meneghesso D, Pennesi M, Pugliese F, Pusceddu S, Ravaioli E, Taroni F, Vergine G, Peruzzi L, Montini G. La Scola C, et al. Pediatr Nephrol. 2022 Sep;37(9):2185-2207. doi: 10.1007/s00467-022-05528-y. Epub 2022 Jun 17. Pediatr Nephrol. 2022. PMID: 35713730 Free PMC article. Review.
The presentation and management of complex female genital malformations.
Acién P, Acién M. Acién P, et al. Hum Reprod Update. 2016 Jan-Feb;22(1):48-69. doi: 10.1093/humupd/dmv048. Epub 2015 Nov 3. Hum Reprod Update. 2016. PMID: 26537987 Review.
Here, we report the clinical presentation and management of: agenesis or hypoplasia of one urogenital ridge; unilateral renal agenesis and ipsilateral blind or obstructed hemivagina or unilateral cervicovaginal agenesis; cavitated and non-communicating …
Here, we report the clinical presentation and management of: agenesis or hypoplasia of one urogenital ridge; unilateral renal …
Herlyn-Werner-Wunderlich syndromne: case review and report of the literature.
Gutiérrez-Montufar OO, Zambrano-Moncayo CP, Otálora-Gallego MC, Meneses-Parra AL, Díaz-Yamal I. Gutiérrez-Montufar OO, et al. Rev Colomb Obstet Ginecol. 2021 Dec 30;72(4):407-422. doi: 10.18597/rcog.3699. Rev Colomb Obstet Ginecol. 2021. PMID: 35134287 Free PMC article. Review. English, Spanish.
CONCLUSION: HWWS is an infrequent disease condition. It must be part of the work-up for renal agenesis in pediatric patients and of the differential diagnosis in primary dysmenorrhea in adolescence. ...CONCLUSION: HWWS is an infrequent disease condition. It must be …
CONCLUSION: HWWS is an infrequent disease condition. It must be part of the work-up for renal agenesis in pediatric patients a …
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. However, the reported prevalences of these anomalies are highly variable. We estimated the prevalence …
BACKGROUND: Unilateral renal agenesis (URA) is associated with other congenital anomalies of the kidney and urinary tract (CAK …
Fetal Therapy for Renal Anhydramnios.
Miller JL, Baschat AA, Atkinson MA. Miller JL, et al. Clin Perinatol. 2022 Dec;49(4):849-862. doi: 10.1016/j.clp.2022.08.001. Epub 2022 Oct 9. Clin Perinatol. 2022. PMID: 36328603 Review.
The most severe forms of congenital anomalies of the kidney and urinary tract present in fetal life with early pregnancy renal anhydramnios and are considered lethal due to pulmonary hypoplasia without fetal therapy. ...Restoring amniotic fluid around the fetus is the prin …
The most severe forms of congenital anomalies of the kidney and urinary tract present in fetal life with early pregnancy renal anhydr …
201 results