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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 6
2024 2

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204 results

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Page 1
The genetics and pathogenesis of CAKUT.
Kolvenbach CM, Shril S, Hildebrandt F. Kolvenbach CM, et al. Nat Rev Nephrol. 2023 Nov;19(11):709-720. doi: 10.1038/s41581-023-00742-9. Epub 2023 Jul 31. Nat Rev Nephrol. 2023. PMID: 37524861 Review.
The clinical spectrum ranges from severe malformations, such as renal agenesis, to potentially milder manifestations, such as vesicoureteral reflux. ...
The clinical spectrum ranges from severe malformations, such as renal agenesis, to potentially milder manifestations, such as …
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, …
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 …
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.
They may be classified as anomalies of renal form, which are subclassified as structural anomalies (eg, persistent fetal lobulation, hypertrophied column of Bertin, and dromedary hump) and fusion anomalies (eg, horseshoe kidney and pancake kidney); anomalies of renal position (eg …
They may be classified as anomalies of renal form, which are subclassified as structural anomalies (eg, persistent fetal lobulation, hypertr …
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.
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 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.
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.
Most congenital cases will be detected during antenatal ultrasound screening, but up to 38% of cases of unilateral renal agenesis are missed. In about 25-50% of cases of antenatally detected SFK there will be signs of hypertrophy, which could indicate additional nep …
Most congenital cases will be detected during antenatal ultrasound screening, but up to 38% of cases of unilateral renal agenesis …
Radial longitudinal deficiency.
Maschke SD, Seitz W, Lawton J. Maschke SD, et al. J Am Acad Orthop Surg. 2007 Jan;15(1):41-52. doi: 10.5435/00124635-200701000-00005. J Am Acad Orthop Surg. 2007. PMID: 17213381 Review.
All children presenting with radial longitudinal deficiency, regardless of severity, require a renal ultrasound, echocardiogram, and complete blood count to evaluate the potential for associated systemic conditions; these include Fanconi's anemia, the Holt-Oram syndrome, and the …
All children presenting with radial longitudinal deficiency, regardless of severity, require a renal ultrasound, echocardiogram, and complet …
Fetal renal impairment.
Vanderheyden T, Kumar S, Fisk NM. Vanderheyden T, et al. Semin Neonatol. 2003 Aug;8(4):279-89. doi: 10.1016/S1084-2756(03)00022-8. Semin Neonatol. 2003. PMID: 15001131 Review.
Causes of prerenal FRI include intrauterine growth restriction, unbalanced intertwin transfusion in monochorionic twins and maternal drug ingestion. Bilateral renal agenesis, multicystic dysplasia and both the autosomal dominant and recessive forms of polycystic kid …
Causes of prerenal FRI include intrauterine growth restriction, unbalanced intertwin transfusion in monochorionic twins and maternal drug in …
204 results