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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 3 |
2010 | 2 |
2011 | 1 |
2012 | 1 |
2013 | 1 |
2024 | 0 |
Search Results
7 results
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Page 1
Mutations in DSTYK and dominant urinary tract malformations.
N Engl J Med. 2013 Aug 15;369(7):621-9. doi: 10.1056/NEJMoa1214479. Epub 2013 Jul 17.
N Engl J Med. 2013.
PMID: 23862974
Free PMC article.
Copy-number disorders are a common cause of congenital kidney malformations.
Sanna-Cherchi S, Kiryluk K, Burgess KE, Bodria M, Sampson MG, Hadley D, Nees SN, Verbitsky M, Perry BJ, Sterken R, Lozanovski VJ, Materna-Kiryluk A, Barlassina C, Kini A, Corbani V, Carrea A, Somenzi D, Murtas C, Ristoska-Bojkovska N, Izzi C, Bianco B, Zaniew M, Flogelova H, Weng PL, Kacak N, Giberti S, Gigante M, Arapovic A, Drnasin K, Caridi G, Curioni S, Allegri F, Ammenti A, Ferretti S, Goj V, Bernardo L, Jobanputra V, Chung WK, Lifton RP, Sanders S, State M, Clark LN, Saraga M, Padmanabhan S, Dominiczak AF, Foroud T, Gesualdo L, Gucev Z, Allegri L, Latos-Bielenska A, Cusi D, Scolari F, Tasic V, Hakonarson H, Ghiggeri GM, Gharavi AG.
Sanna-Cherchi S, et al.
Am J Hum Genet. 2012 Dec 7;91(6):987-97. doi: 10.1016/j.ajhg.2012.10.007. Epub 2012 Nov 15.
Am J Hum Genet. 2012.
PMID: 23159250
Free PMC article.
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'Congenital solitary functioning kidneys: which ones warrant follow-up into adult life?'.
Corbani V, Ghiggeri GM, Sanna-Cherchi S.
Corbani V, et al.
Nephrol Dial Transplant. 2011 May;26(5):1458-60. doi: 10.1093/ndt/gfr145. Epub 2011 Apr 5.
Nephrol Dial Transplant. 2011.
PMID: 21467130
No abstract available.
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Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract.
Gimelli S, Caridi G, Beri S, McCracken K, Bocciardi R, Zordan P, Dagnino M, Fiorio P, Murer L, Benetti E, Zuffardi O, Giorda R, Wells JM, Gimelli G, Ghiggeri GM.
Gimelli S, et al.
Hum Mutat. 2010 Dec;31(12):1352-9. doi: 10.1002/humu.21378. Epub 2010 Nov 9.
Hum Mutat. 2010.
PMID: 20960469
Free PMC article.
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Five cases of severe vesico-ureteric reflux in a family with an X-linked compatible trait.
Naseri M, Ghiggeri GM, Caridi G, Abbaszadegan MR.
Naseri M, et al.
Pediatr Nephrol. 2010 Feb;25(2):349-52. doi: 10.1007/s00467-009-1293-8. Epub 2009 Aug 25.
Pediatr Nephrol. 2010.
PMID: 19705159
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Combinatorial peptide ligand libraries for urine proteome analysis: investigation of different elution systems.
Candiano G, Dimuccio V, Bruschi M, Santucci L, Gusmano R, Boschetti E, Righetti PG, Ghiggeri GM.
Candiano G, et al.
Electrophoresis. 2009 Jul;30(14):2405-11. doi: 10.1002/elps.200800762.
Electrophoresis. 2009.
PMID: 19593750
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Renal outcome in patients with congenital anomalies of the kidney and urinary tract.
Sanna-Cherchi S, Ravani P, Corbani V, Parodi S, Haupt R, Piaggio G, Innocenti ML, Somenzi D, Trivelli A, Caridi G, Izzi C, Scolari F, Mattioli G, Allegri L, Ghiggeri GM.
Sanna-Cherchi S, et al.
Kidney Int. 2009 Sep;76(5):528-33. doi: 10.1038/ki.2009.220. Epub 2009 Jun 17.
Kidney Int. 2009.
PMID: 19536081
Free article.
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