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

Year Number of Results
1963 1
1964 8
1965 1
1966 1
1967 1
1968 7
1969 2
1970 10
1971 11
1972 7
1973 12
1974 11
1975 2
1976 13
1977 7
1978 6
1979 12
1980 4
1981 15
1982 9
1983 7
1984 11
1985 15
1986 11
1987 14
1988 24
1989 25
1990 23
1991 31
1992 33
1993 46
1994 36
1995 42
1996 36
1997 57
1998 48
1999 37
2000 35
2001 43
2002 30
2003 36
2004 27
2005 30
2006 36
2007 39
2008 54
2009 40
2010 47
2011 68
2012 55
2013 62
2014 85
2015 57
2016 54
2017 62
2018 59
2019 46
2020 64
2021 54
2022 55
2023 55
2024 24

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1,695 results

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Page 1
Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT).
Rodriguez MM. Rodriguez MM. Fetal Pediatr Pathol. 2014 Oct-Dec;33(5-6):293-320. doi: 10.3109/15513815.2014.959678. Epub 2014 Oct 14. Fetal Pediatr Pathol. 2014. PMID: 25313840 Free PMC article. Review.
This article reviews the majority of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) with emphasis in Pediatric Pathology describing and illustrating lesions as varied as ureteral duplications, ureteropelvic junction obstruction, horseshoe …
This article reviews the majority of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) with emphasis …
Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT).
Talati AN, Webster CM, Vora NL. Talati AN, et al. Prenat Diagn. 2019 Aug;39(9):679-692. doi: 10.1002/pd.5536. Epub 2019 Aug 5. Prenat Diagn. 2019. PMID: 31343747 Free PMC article. Review.
Congenital anomalies of the kidney and urinary tract (CAKUT) constitute 20% of all congenital malformations occurring in one in 500 live births. ...Pathogenic variants in genes causing CAKUT include monogenic diseases such as polycystic kidne
Congenital anomalies of the kidney and urinary tract (CAKUT) constitute 20% of all congenital malformatio
A Primer on Congenital Anomalies of the Kidneys and Urinary Tracts (CAKUT).
Murugapoopathy V, Gupta IR. Murugapoopathy V, et al. Clin J Am Soc Nephrol. 2020 May 7;15(5):723-731. doi: 10.2215/CJN.12581019. Epub 2020 Mar 18. Clin J Am Soc Nephrol. 2020. PMID: 32188635 Free PMC article. Review.
Congenital anomalies of the kidneys and urinary tracts (CAKUT) are disorders caused by defects in the development of the kidneys and their outflow tracts. ...In severe cases of CAKUT, when the kidneys do not form, the fetus will not survive. How
Congenital anomalies of the kidneys and urinary tracts (CAKUT) are disorders caused by defects in the development of th
Glomerular hyperfiltration.
Cortinovis M, Perico N, Ruggenenti P, Remuzzi A, Remuzzi G. Cortinovis M, et al. Nat Rev Nephrol. 2022 Jul;18(7):435-451. doi: 10.1038/s41581-022-00559-y. Epub 2022 Apr 1. Nat Rev Nephrol. 2022. PMID: 35365815 Review.
Thus, when the single-nephron GFR is increased in the context of a normal number of functioning nephrons, single glomerular hyperfiltration results in 'absolute' hyperfiltration in the kidney. 'Absolute' hyperfiltration can occur in healthy people after high protein intake …
Thus, when the single-nephron GFR is increased in the context of a normal number of functioning nephrons, single glomerular hyperfiltration …
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.
Congenital anomalies of the kidney and urinary tract (CAKUT) comprise a large variety of malformations that arise from defective kidney or urinary tract development and frequently lead to kidney failure. The clinical spectru
Congenital anomalies of the kidney and urinary tract (CAKUT) comprise a large variety of malformations that aris
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.
The upper urinary tract is the most common human system affected by congenital anomalies. ...Comprehension of congenital anomalies of the upper urinary tract is crucial for an accurate diagnosis and correct management. ...
The upper urinary tract is the most common human system affected by congenital anomalies. ...Comprehension of congen
The etiology of VACTERL association: Current knowledge and hypotheses.
Solomon BD. Solomon BD. Am J Med Genet C Semin Med Genet. 2018 Dec;178(4):440-446. doi: 10.1002/ajmg.c.31664. Am J Med Genet C Semin Med Genet. 2018. PMID: 30580478 Review.
VACTERL association is a condition involving the presence of multiple congenital anomalies. The condition was first described more than four decades ago, and is not extremely rare. ...
VACTERL association is a condition involving the presence of multiple congenital anomalies. The condition was first described more th …
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.
In recent years, several studies have been published on the prognosis of children with congenital solitary kidney (CSK), with controversial results, and a worldwide consensus on management and follow-up is lacking. ...We recommend that any antenatal suspicion/diagno …
In recent years, several studies have been published on the prognosis of children with congenital solitary kidney (CSK), with …
Renal-skin syndromes.
Has C, He Y. Has C, et al. Cell Tissue Res. 2017 Jul;369(1):63-73. doi: 10.1007/s00441-017-2623-y. Epub 2017 Apr 22. Cell Tissue Res. 2017. PMID: 28432467 Review.
We provide a non-exhaustive overview of the main molecular players at cell-matrix adhesions in mouse models and in human genetic disorders affecting kidney and skin. Renal and urinary tract involvement is described in all four major epidermolysis bullosa type …
We provide a non-exhaustive overview of the main molecular players at cell-matrix adhesions in mouse models and in human genetic disorders a …
The genetic basis of congenital anomalies of the kidney and urinary tract.
Kagan M, Pleniceanu O, Vivante A. Kagan M, et al. Pediatr Nephrol. 2022 Oct;37(10):2231-2243. doi: 10.1007/s00467-021-05420-1. Epub 2022 Feb 4. Pediatr Nephrol. 2022. PMID: 35122119 Review.
During the past decades, remarkable progress has been made in our understanding of the molecular basis of kidney diseases, as well as in the ability to pinpoint disease-causing genetic changes. Congenital anomalies of the kidney and urinary tract
During the past decades, remarkable progress has been made in our understanding of the molecular basis of kidney diseases, as well as …
1,695 results