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

Year Number of Results
1999 1
2003 4
2006 1
2009 2
2010 5
2011 5
2012 5
2013 7
2014 16
2015 15
2016 11
2017 17
2018 12
2019 10
2020 25
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Similar Articles for PMID: 32312792

114 results
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Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract.
Westland R, Renkema KY, Knoers NVAM. Westland R, et al. Clin J Am Soc Nephrol. 2020 Apr 20:CJN.14661119. doi: 10.2215/CJN.14661119. Online ahead of print. Clin J Am Soc Nephrol. 2020. PMID: 32312792
Congenital Anomalies of the Kidney and Urinary Tract in Children Born Small for Gestational Age.
Janchevska A, Gucev Z, Tasevska-Rmus L, Tasic V. Janchevska A, et al. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017 Mar 1;38(1):53-57. doi: 10.1515/prilozi-2017-0007. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017. PMID: 28593895
Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract.
Lee KH, Gee HY, Shin JI. Lee KH, et al. Investig Clin Urol. 2017 Jun;58(Suppl 1):S4-S13. doi: 10.4111/icu.2017.58.S1.S4. Epub 2017 Jun 7. Investig Clin Urol. 2017. PMID: 28612055 Free PMC article. Review.
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 Review.
Impact of next generation sequencing on our understanding of CAKUT.
Nigam A, Knoers NVAM, Renkema KY. Nigam A, et al. Semin Cell Dev Biol. 2019 Jul;91:104-110. doi: 10.1016/j.semcdb.2018.08.013. Epub 2018 Sep 5. Semin Cell Dev Biol. 2019. PMID: 30172048 Review.
[Genetic Basis of Congenital Anomalies of the Kidney and Urinary Tract].
Bodria M, Sanna-Cherchi S. Bodria M, et al. G Ital Nefrol. 2015;32 Suppl 64:gin/32.S64.16. G Ital Nefrol. 2015. PMID: 26479062 Review. Italian.
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, Hwang DY, Schulz J, Braun DA, Schmidt JM, Schapiro D, Schneider R, Warejko JK, Daga A, Majmundar AJ, Tan W, Jobst-Schwan T, Hermle T, Widmeier E, Ashraf S, Amar A, Hoogstraaten CA, Hugo H, Kitzler TM, Kause F, Kolvenbach CM, Dai R, Spaneas L, Amann K, Stein DR, Baum MA, Somers MJG, Rodig NM, Ferguson MA, Traum AZ, Daouk GH, Bogdanović R, Stajić N, Soliman NA, Kari JA, El Desoky S, Fathy HM, Milosevic D, Al-Saffar M, Awad HS, Eid LA, Selvin A, Senguttuvan P, Sanna-Cherchi S, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Wilson MW, Mane SM, Lifton RP, Lee RS, Bauer SB, Lu W, Reutter HM, Tasic V, Shril S, Hildebrandt F. van der Ven AT, et al. J Am Soc Nephrol. 2018 Sep;29(9):2348-2361. doi: 10.1681/ASN.2017121265. Epub 2018 Aug 24. J Am Soc Nephrol. 2018. PMID: 30143558 Free PMC article.
Congenital Anomalies of the Kidney and Urinary Tract: A Clinical Review.
Stonebrook E, Hoff M, Spencer JD. Stonebrook E, et al. Curr Treat Options Pediatr. 2019;5(3):223-235. doi: 10.1007/s40746-019-00166-3. Epub 2019 Jun 11. Curr Treat Options Pediatr. 2019. PMID: 32864297 Free PMC article.
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
Le Tanno P, Breton J, Bidart M, Satre V, Harbuz R, Ray PF, Bosson C, Dieterich K, Jaillard S, Odent S, Poke G, Beddow R, Digilio MC, Novelli A, Bernardini L, Pisanti MA, Mackenroth L, Hackmann K, Vogel I, Christensen R, Fokstuen S, Béna F, Amblard F, Devillard F, Vieville G, Apostolou A, Jouk PS, Guebre-Egziabher F, Sartelet H, Coutton C. Le Tanno P, et al. J Med Genet. 2017 Jul;54(7):502-510. doi: 10.1136/jmedgenet-2016-104435. Epub 2017 Mar 7. J Med Genet. 2017. PMID: 28270404
High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT.
Bulum B, Ozçakar ZB, Ustüner E, Düşünceli E, Kavaz A, Duman D, Walz K, Fitoz S, Tekin M, Yalçınkaya F. Bulum B, et al. Pediatr Nephrol. 2013 Nov;28(11):2143-7. doi: 10.1007/s00467-013-2530-8. Epub 2013 Jun 28. Pediatr Nephrol. 2013. PMID: 23812353
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