Fondo malattie renali del bambino - Fondazione malattie renali del bambino
Pubblicazioni 2011
Fondo Malattie Renali del Bambino - Fondazione Malattie Renali del Bambino - Istituto Gaslini Genova

Pubblicazioni 2011

1. Aloi C, Salina A, Pasquali L, Lugani F, Perri K, Russo C, Tallone R, Ghiggeri GM, Lorini R, and d’Annunzio G, Wolfram syndrome: new mutations, different phenotype. PLoS One, 2012. 7(1): p. e29150.

2. Bonthuis M, van Stralen KJ, Verrina E, Edefonti A, Molchanova EA, Hokken-Koelega AC, Schaefer F, and Jager KJ, Use of national and international growth charts for studying height in European children: development of up-to-date European height-for-age charts. PLoS One, 2012. 7(8): p. e42506.

3. Candiano G, Santucci L, Bruschi M, Petretto A, D’Ambrosio C, Scaloni A, Righetti PG, and Ghiggeri GM, "Cheek-to-cheek" urinary proteome profiling via combinatorial peptide ligand libraries: A novel, unexpected elution system. J Proteomics, 2012. 75(3): p. 796-805.

4. Caridi G, Dagnino M, Di Duca M, Akyuz F, Boztas G, Besisik F, Demir K, Ormeci A, Gokturk S, Cefle K, Ozturk S, Palanduz S, Campagnoli M, Galliano M, and Minchiotti L, A novel two bases deletion in the albumin gene causes analbuminaemia in a young Turkish man. Clin Chim Acta, 2012. 413(9-10): p. 950-1.

5. Caridi G, Dagnino M, Di Duca M, Pinto H, Espinheira Mdo C, Guerra A, Fernandes S, Campagnoli M, Galliano M, and Minchiotti L, A novel splicing mutation causes analbuminemia in a Portuguese boy. Mol Genet Metab, 2012. 105(3): p. 479-83.

6. Caridi G, Dagnino M, Duca MD, Santra S, Ball S, Sulaiman RA, Campagnoli M, Galliano M, and Minchiotti L, A two-base-pairs deletion in the albumin gene causes a new case of analbuminemia. Clin Chem Lab Med, 2012.

7. Comoli P and Ginevri F, Monitoring and managing viral infections in pediatric renal transplant recipients. Pediatr Nephrol, 2012. 27(5): p. 705-17.

8. Ginevri F, Nocera A, Comoli P, Innocente A, Cioni M, Parodi A, Fontana I, Magnasco A, Nocco A, Tagliamacco A, Sementa A, Ceriolo P, Ghio L, Zecca M, Cardillo M, Garibotto G, Ghiggeri GM, and Poli F, Posttransplant De Novo Donor-Specific HLA Antibodies Identify Pediatric Kidney Recipients at Risk for Late Antibody-Mediated Rejection. Am J Transplant, 2012.

9. Ginocchio F, Verrina E, Furfaro E, Cannavo R, Bandettini R, and Castagnola E, Case report of the reliability 1,3-beta-D-glucan monitoring during treatment of peritoneal candidiasis in a child receiving continuous peritoneal dialysis. Clin Vaccine Immunol, 2012. 19(4): p. 626-7.

10. Grossi PA, Costa AN, Fehily D, Blumberg EA, Kuehnert MJ, Fishman JA, Ison MG, Lattes R, Kotton CN, Lilleri D, Kabanova A, Lanzavecchia A, Gerna G, Razonable RR, Comoli P, Zecca M, Basso S, Ginevri F, Grossi A, Schena FP, Rimola A, Burra P, De Martin E, Rodriguez-Castro KI, Fagiuoli S, Pasulo L, Bruno R, Andreone P, Loggi E, Arena F, Maria Rossolini G, Sganga G, and Cozza V, Infections and organ transplantation: new challenges for prevention and treatment--a colloquium. Transplantation, 2012. 93(5 Suppl): p. S4-S39.

11. Harambat J, van Stralen KJ, Espinosa L, Groothoff JW, Hulton SA, Cerkauskiene R, Schaefer F, Verrina E, Jager KJ, and Cochat P, Characteristics and outcomes of children with primary oxalosis requiring renal replacement therapy. Clin J Am Soc Nephrol, 2012. 7(3): p. 458-65.

12. Kramer A, Stel VS, Geskus RB, Tizard EJ, Verrina E, Schaefer F, Heaf JG, Kramar R, Krischock L, Leivestad T, Palsson R, Ravani P, and Jager KJ, The effect of timing of the first kidney transplantation on survival in children initiating renal replacement therapy. Nephrol Dial Transplant, 2012. 27(3): p. 1256-64.

13. Magnasco A, Ravani P, Edefonti A, Murer L, Ghio L, Belingheri M, Benetti E, Murtas C, Messina G, Massella L, Porcellini MG, Montagna M, Regazzi M, Scolari F, and Ghiggeri GM, Rituximab in children with resistant idiopathic nephrotic syndrome. J Am Soc Nephrol, 2012. 23(6): p. 1117-24.

14. Mattioli G, Guida E, Rossi V, Podesta E, Jasonni V, and Ghiggeri GM, Intraureteral Injection of NASHA/Dx Gel Under Direct Ureteroscopic Visualization for the Treatment of Primary High-Grade Vesicoureteral Reflux. J Laparoendosc Adv Surg Tech A, 2012. 22(8): p. 844-7.

15. Murtas C, Bruschi M, Candiano G, Moroni G, Magistroni R, Magnano A, Bruno F, Radice A, Furci L, Argentiero L, Carnevali ML, Messa P, Scolari F, Sinico RA, Gesualdo L, Fervenza FC, Allegri L, Ravani P, and Ghiggeri GM, Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy. Clin J Am Soc Nephrol, 2012. 7(9): p. 1394-400.

16. Sanna-Cherchi S, Kiryluk K, Burgess Katelyn E, Bodria M, Sampson Matthew G, Hadley D, Nees Shannon N, Verbitsky M, Perry Brittany J, Sterken R, Lozanovski Vladimir J, 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 Patricia L, 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 Wendy K, Lifton Richard P, Sanders S, State M, Clark Lorraine N, Saraga M, Padmanabhan S, Dominiczak Anna F, Foroud T, Gesualdo L, Gucev Z, Allegri L, Latos-Bielenska A, Cusi D, Scolari F, Tasic V, Hakonarson H, Ghiggeri Gian M, and Gharavi Ali G, Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations. American journal of human genetics, 2012.

17. Santucci L, Candiano G, Bruschi M, Bodria M, Murtas C, Petretto A, and Ghiggeri GM, Urinary proteome in a snapshot: normal urine and glomerulonephritis. J Nephrol, 2012: p. 0.

18. Santucci L, Candiano G, Bruschi M, D’Ambrosio C, Petretto A, Scaloni A, Urbani A, Righetti PG, and Ghiggeri GM, Combinatorial peptide ligand libraries for the analysis of low-expression proteins: Validation for normal urine and definition of a first protein MAP. Proteomics, 2012. 12(4-5): p. 509-15.

19. Schaeffer C, Cattaneo A, Trudu M, Santambrogio S, Bernascone I, Giachino D, Caridi G, Campo A, Murtas C, Benoni S, Izzi C, De Marchi M, Amoroso A, Ghiggeri GM, Scolari F, Bachi A, and Rampoldi L, [Mutant uromodulin is secreted in the urine of patients with familial hyperuricemic nephropathy and induces the formation of extracellular aggregates]. G Ital Nefrol, 2012. 29(2): p. 137-41.

20. Schaeffer C, Cattaneo A, Trudu M, Santambrogio S, Bernascone I, Giachino D, Caridi G, Campo A, Murtas C, Benoni S, Izzi C, De Marchi M, Amoroso A, Ghiggeri GM, Scolari F, Bachi A, and Rampoldi L, Urinary secretion and extracellular aggregation of mutant uromodulin isoforms. Kidney Int, 2012. 81(8): p. 769-78.

21. Trachtman H, Gipson DS, Kaskel F, Ghiggeri GM, Faul C, Gupta V, Fornoni A, Burke GW, 3rd, Thomas DB, Barisoni L, Schaefer F, Wei C, and Reiser J, Regarding Maas’s editorial letter on serum suPAR levels. Kidney Int, 2012. 82(4): p. 492.

22. van Stralen KJ, Krischock L, Schaefer F, Verrina E, Groothoff JW, Evans J, Heaf J, Ivanov D, Kostic M, Maringhini S, Podracka L, Printza N, Pundziene B, Reusz GS, Vondrak K, Jager KJ, and Tizard AE, Prevalence and predictors of the sub-target Hb level in children on dialysis. Nephrol Dial Transplant, 2012. 27(10): p. 3950-3957.

23. Verrina EE, Cannavo R, Schaefer B, and Schmitt CP, Are current peritoneal dialysis solutions adequate for pediatric use? Contrib Nephrol, 2012. 178: p. 16-22.

24. Vidal E, Edefonti A, Murer L, Gianoglio B, Maringhini S, Pecoraro C, Sorino P, Leozappa G, Lavoratti G, Ratsch IM, Chimenz R, and Verrina E, Peritoneal dialysis in infants: the experience of the Italian Registry of Paediatric Chronic Dialysis. Nephrol Dial Transplant, 2012. 27(1): p. 388-95.

25. Warady BA, Bakkaloglu S, Newland J, Cantwell M, Verrina E, Neu A, Chadha V, Yap HK, and Schaefer F, Consensus guidelines for the prevention and treatment of catheter-related infections and peritonitis in pediatric patients receiving peritoneal dialysis: 2012 update. Perit Dial Int, 2012. 32 Suppl 2: p. S32-86.

26. Wei C, Trachtman H, Li J, Dong C, Friedman AL, Gassman JJ, McMahan JL, Radeva M, Heil KM, Trautmann A, Anarat A, Emre S, Ghiggeri GM, Ozaltin F, Haffner D, Gipson DS, Kaskel F, Fischer DC, Schaefer F, and Reiser J, Circulating suPAR in Two Cohorts of Primary FSGS. J Am Soc Nephrol, 2012.

27. Wuhl E, van Stralen KJ, Verrina E, Bjerre A, Wanner C, Heaf JG, Zurriaga O, Hoitsma A, Niaudet P, Palsson R, Ravani P, Jager KJ, and Schaefer F, Timing and Outcome of Renal Replacement Therapy in Patients with Congenital Malformations of the Kidney and Urinary Tract. Clin J Am Soc Nephrol, 2012.

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