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Journal Abstract Search

339 related items for PubMed ID: 22245908

  • 1. Novel genetic aspects of congenital anomalies of kidney and urinary tract.
    Weber S.
    Curr Opin Pediatr; 2012 Apr; 24(2):212-8. PubMed ID: 22245908
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  • 5. Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT).
    Renkema KY, Winyard PJ, Skovorodkin IN, Levtchenko E, Hindryckx A, Jeanpierre C, Weber S, Salomon R, Antignac C, Vainio S, Schedl A, Schaefer F, Knoers NV, Bongers EM, EUCAKUT consortium.
    Nephrol Dial Transplant; 2011 Dec; 26(12):3843-51. PubMed ID: 22121240
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  • 6. Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.
    Capone VP, Morello W, Taroni F, Montini G.
    Int J Mol Sci; 2017 Apr 11; 18(4):. PubMed ID: 28398236
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  • 8. Congenital anomalies of the kidney and urinary tract--role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene.
    Pope JC, Brock JW, Adams MC, Miyazaki Y, Stephens FD, Ichikawa I.
    J Urol; 2001 Jan 11; 165(1):196-202. PubMed ID: 11125405
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  • 9. Genetics of congenital anomalies of the kidney and urinary tract.
    Song R, Yosypiv IV.
    Pediatr Nephrol; 2011 Mar 11; 26(3):353-64. PubMed ID: 20798957
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  • 10. Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract.
    Kohl S, Chen J, Vivante A, Hwang DY, Shril S, Dworschak GC, Van Der Ven A, Sanna-Cherchi S, Bauer SB, Lee RS, Soliman NA, Kehinde EO, Reutter HM, Tasic V, Hildebrandt F.
    Nephrol Dial Transplant; 2016 Aug 11; 31(8):1280-3. PubMed ID: 26908769
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  • 11. 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.
    J Med Genet; 2017 Jul 11; 54(7):502-510. PubMed ID: 28270404
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  • 12. The renin-angiotensin system in the development of the congenital anomalies of the kidney and urinary tract.
    Niimura F, Kon V, Ichikawa I.
    Curr Opin Pediatr; 2006 Apr 11; 18(2):161-6. PubMed ID: 16601496
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  • 13. Pattern of clinical presentation of congenital anomalies of the kidney and urinary tract among infants and children.
    Soliman NA, Ali RI, Ghobrial EE, Habib EI, Ziada AM.
    Nephrology (Carlton); 2015 Jun 11; 20(6):413-8. PubMed ID: 25645028
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  • 14. 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.
    J Am Soc Nephrol; 2018 Sep 11; 29(9):2348-2361. PubMed ID: 30143558
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  • 15. Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung's disease: a systematic review.
    Hofmann AD, Duess JW, Puri P.
    Pediatr Surg Int; 2014 Aug 11; 30(8):757-61. PubMed ID: 24974188
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  • 16. Congenital anomalies of the kidney and urinary tract genetics in mice and men.
    Caruana G, Bertram JF.
    Nephrology (Carlton); 2015 May 11; 20(5):309-11. PubMed ID: 25605230
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  • 17. Plumbing in the embryo: developmental defects of the urinary tracts.
    Uetani N, Bouchard M.
    Clin Genet; 2009 Apr 11; 75(4):307-17. PubMed ID: 19419410
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  • 18. Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
    Kohl S, Hwang DY, Dworschak GC, Hilger AC, Saisawat P, Vivante A, Stajic N, Bogdanovic R, Reutter HM, Kehinde EO, Tasic V, Hildebrandt F.
    J Am Soc Nephrol; 2014 Sep 11; 25(9):1917-22. PubMed ID: 24700879
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  • 19. PAX2 gene mutations in pediatric and young adult transplant recipients: kidney and urinary tract malformations without ocular anomalies.
    Negrisolo S, Benetti E, Centi S, Della Vella M, Ghirardo G, Zanon GF, Murer L, Artifoni L.
    Clin Genet; 2011 Dec 11; 80(6):581-5. PubMed ID: 21108633
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  • 20. Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
    Vivante A, Kohl S, Hwang DY, Dworschak GC, Hildebrandt F.
    Pediatr Nephrol; 2014 Apr 11; 29(4):695-704. PubMed ID: 24398540
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