Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2006 1
2007 2
2008 2
2009 3
2010 4
2011 2
2012 4
2013 3
2014 8
2015 6
2016 11
2017 4
2018 6
2019 11
2020 12
2021 16
2022 17
2023 17
2024 5

Text availability

Article attribute

Article type

Publication date

Search Results

102 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Congenital anomalies of kidney and urinary tract 2"
Page 1
Congenital anomalies of the urinary tract.
Pohl HG, Belman AB. Pohl HG, et al. Curr Pediatr Rev. 2014;10(2):123-32. doi: 10.2174/157339631002140513102152. Curr Pediatr Rev. 2014. PMID: 25088266 Review.
Instead, further radiographic imaging is required to delineate anatomy and function. Now, moreover, non-surgical management of CAKUT should be considered whenever possible. Despite the widespread use of prenatal screening sonography that usually identifies the majority of …
Instead, further radiographic imaging is required to delineate anatomy and function. Now, moreover, non-surgical management of CAKUT
Dysplastic kidneys.
Winyard P, Chitty LS. Winyard P, et al. Semin Fetal Neonatal Med. 2008 Jun;13(3):142-51. doi: 10.1016/j.siny.2007.10.009. Epub 2007 Dec 11. Semin Fetal Neonatal Med. 2008. PMID: 18065301 Review.
They are part of the spectrum of Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) and an increasing number of children are being diagnosed on antenatal ultrasound. ...Postnatal investigations aim to define the anatomy, which helps to estimate risks of infec …
They are part of the spectrum of Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) and an increasing number of childre …
The term CAKUT has outlived its usefulness: the case for the prosecution.
Woolf AS. Woolf AS. Pediatr Nephrol. 2022 Nov;37(11):2785-2791. doi: 10.1007/s00467-022-05576-4. Epub 2022 May 16. Pediatr Nephrol. 2022. PMID: 35575937 Free PMC article. Review.
Moreover, the angiotensin II receptor type 2 was seen as a paradigmatic molecule in the pathobiology of CAKUT. ...To reach these conclusions, I focus on the complex of research observations that led to the theory behind CAKUT, and then question whether …
Moreover, the angiotensin II receptor type 2 was seen as a paradigmatic molecule in the pathobiology of CAKUT. ...To reach the …
Congenital Solitary Functioning Kidney: A Review.
Wakabayashi EA, Pantaleão AN, Avendanha RA, Brunheroto FB, Simões E Silva AC. Wakabayashi EA, et al. Curr Med Chem. 2023;30(2):203-219. doi: 10.2174/0929867329666220629142556. Curr Med Chem. 2023. PMID: 35770397 Review.
BACKGROUND: Solitary functioning kidney (SFK) is a subgroup of the Congenital Anomalies of the Kidneys and Urinary Tract (CAKUT). Although the prognosis of these patients was considered good in the past, numerous studies have shown different levels of kidney damage associa …
BACKGROUND: Solitary functioning kidney (SFK) is a subgroup of the Congenital Anomalies of the Kidneys and Urinary Tract (CAKUT). Alt …
Predicting outcomes in children with congenital anomalies of the kidney and urinary tract.
Matsell DG, Catapang M, Becknell B. Matsell DG, et al. Pediatr Nephrol. 2023 Oct;38(10):3407-3415. doi: 10.1007/s00467-023-05992-0. Epub 2023 May 3. Pediatr Nephrol. 2023. PMID: 37133803 Free PMC article.
Using a large CAKUT cohort, we sought to identify the predictors of CKD and to develop a prediction model that informs a risk-stratified clinical pathway. ...PUV (OR 4.7, 95% CI 1.5-15.3), first eGFR <90 (OR 4.4, 95% CI 2-9.7), and kidney length to …
Using a large CAKUT cohort, we sought to identify the predictors of CKD and to develop a prediction model that informs …
Evaluation and fetal intervention in severe fetal hydronephrosis.
Safdar A, Singh K, Sun RC, Nassr AA. Safdar A, et al. Curr Opin Pediatr. 2021 Apr 1;33(2):220-226. doi: 10.1097/MOP.0000000000001001. Curr Opin Pediatr. 2021. PMID: 33651757 Review.
A prenatal diagnosis of CAKUT can have an early fetal intervention to minimize these consequences. This review aims to provide an overview of the possible fetal intervention with severe hydronephrosis. RECENT FINDINGS: Clinical course and outcomes of CAKUT are pr
A prenatal diagnosis of CAKUT can have an early fetal intervention to minimize these consequences. This review aims to provide an ove …
Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformations.
Khan K, Ahram DF, Liu YP, Westland R, Sampogna RV, Katsanis N, Davis EE, Sanna-Cherchi S. Khan K, et al. Kidney Int. 2022 Mar;101(3):473-484. doi: 10.1016/j.kint.2021.09.034. Epub 2021 Nov 12. Kidney Int. 2022. PMID: 34780871 Free PMC article. Review.
Advances in clinical diagnostics and molecular tools have improved our understanding of the genetically heterogeneous causes underlying congenital anomalies of kidney and urinary tract (CAKUT). However, despite a sharp incli …
Advances in clinical diagnostics and molecular tools have improved our understanding of the genetically heterogeneous causes underlying c
Primary causes of kidney disease and mortality in dialysis-dependent children.
Okuda Y, Soohoo M, Ishikura K, Tang Y, Obi Y, Laster M, Rhee CM, Streja E, Kalantar-Zadeh K. Okuda Y, et al. Pediatr Nephrol. 2020 May;35(5):851-860. doi: 10.1007/s00467-019-04457-7. Epub 2020 Feb 4. Pediatr Nephrol. 2020. PMID: 32020338 Free PMC article.
RESULTS: Among 25,761 patients, the median (interquartile range) age was 17 (11-19) years, and 4780 (19%) had CAKUT. CAKUT was associated with lower mortality, with an adjusted hazard ratio (aHR) of 0.72 (95%CI, 0.64-0.81) (reference: non-CAKUT). ...While the …
RESULTS: Among 25,761 patients, the median (interquartile range) age was 17 (11-19) years, and 4780 (19%) had CAKUT. CAKUT was …
Widespread kidney anomalies in children with Down syndrome.
Postolache L, Parsa A, Simoni P, Boitsios G, Ismaili K, Schurmans T, Monier A, Casimir G, Albert A, Parsa CF. Postolache L, et al. Pediatr Nephrol. 2022 Oct;37(10):2361-2368. doi: 10.1007/s00467-022-05455-y. Epub 2022 Feb 3. Pediatr Nephrol. 2022. PMID: 35118542
BACKGROUND: Rare autopsy studies have described smaller kidneys as well as urinary tract anomalies in Down syndrome. This observation has never been investigated in vivo and little is known about the possible consequences upon kidney function. ...Twenty-one of the children …
BACKGROUND: Rare autopsy studies have described smaller kidneys as well as urinary tract anomalies in Down syndrome. This observation
Life expectancy with chronic kidney disease: an educational review.
Neild GH. Neild GH. Pediatr Nephrol. 2017 Feb;32(2):243-248. doi: 10.1007/s00467-016-3383-8. Epub 2016 Apr 26. Pediatr Nephrol. 2017. PMID: 27115888 Free PMC article. Review.
Can renal prognosis and life expectancy be accurately predicted? Increasingly, the answer is yes. The natural history of different forms of renal disease is becoming clearer; the degree of reduction in glomerular filtration rate (GFR) and the magnitude of proteinuria are s …
Can renal prognosis and life expectancy be accurately predicted? Increasingly, the answer is yes. The natural history of different fo …
102 results