Fondo malattie renali del bambino - Fondazione malattie renali del bambino
Pubblicazioni 2014
Fondo Malattie Renali del Bambino - Fondazione Malattie Renali del Bambino - Istituto Gaslini Genova

Pubblicazioni 2014

Con la partecipazione attiva della nostra Fondazione

 1)   M. Bruschi, M. Galetti, R. A. Sinico, G. Moroni, A. Bonanni, A. Radice, A. Tincani, F. Pratesi, P. Migliorini, C. Murtas, F. Franceschini, B. Trezzi, F. Brunini, R. Gatti, R. Tardanico, G. Barbano, G. Piaggio, P. Messa, P. Ravani, F. Scolari, G. Candiano, A. Martini, L. Allegri, and G. M. Ghiggeri, "Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens," J Am Soc Nephrol (2014)

2)  M. Bruschi, R. A. Sinico, G. Moroni, F. Pratesi, P. Migliorini, M. Galetti, C. Murtas, A. Tincani, M. Madaio, A. Radice, F. Franceschini, B. Trezzi, L. Bianchi, A. Giallongo, R. Gatti, R. Tardanico, A. Scaloni, C. D’Ambrosio, M. L. Carnevali, P. Messa, P. Ravani, G. Barbano, B. Bianco, A. Bonanni, F. Scolari, A. Martini, G. Candiano, L. Allegri, and G. M. Ghiggeri, "Glomerular autoimmune multicomponents of human lupus nephritis in vivo: alpha-enolase and annexin AI," J Am Soc Nephrol 25 (11), 2483-2498 (2014)

3)   A. Bonanni, A. Vaglio, M. Bruschi, R. A. Sinico, L. Cavagna, G. Moroni, F. Franceschini, L. Allegri, F. Pratesi, P. Migliorini, G. Candiano, G. Pesce, A. Ravelli, F. Puppo, A. Martini, A. Tincani, and G. M. Ghiggeri, "Multi-antibody composition in lupus nephritis: Isotype and antigen specificity make the difference," Autoimmun Rev (2015)

4)  I. Panfoli, M. Bruschi, L. Santucci, D. Calzia, S. Ravera, A. Petretto, and G. Candiano, "Myelin proteomics: the past, the unexpected and the future," Expert Rev Proteomics 11 (3), 345-354 (2014)

5)  M. Bruschi, S. Ravera,L. Santucci,G. Candiano, M. Bartolucci, D. Calzia,C. Lavarello, E. Inglese, A. Petretto, G.M. Ghiggeri, I. Panfoli.HUMAN URINARY EXOSOME AS A METABOLIC EFFECTOR CARGO”Expert Rev Proteomics (2015)

6)  G. Candiano, L. Santucci, A. Petretto, C. Lavarello, E. Inglese, M. Bruschi, G. M. Ghiggeri, E. Boschetti, and P. G. Righetti, "Widening and Diversifying the Proteome Capture by Combinatorial Peptide Ligand Libraries via Alcian Blue Dye Binding," Anal Chem 87 (9), 4814-4820 (2015)

7)  L. Santucci, G. Candiano, A. Petretto, M. Bruschi, C. Lavarello, E. Inglese, P. G. Righetti, and G. M. Ghiggeri, "From hundreds to thousands: Widening the normal human Urinome (1)," J Proteomics 112, 53-62 (2015)

8)  M. Bruschi, G. Candiano, L. Santucci, C. D’Ambrosio, A. Scaloni, M. Bonsano, G. M. Ghiggeri, and E. Verrina, "Combinatorial Peptide Ligand Library and two dimensional electrophoresis: new frontiers in the study of peritoneal dialysis effluent in pediatric patients,"J Proteomics 116, 68-80 (2015)

9)  M. Bruschi, L. Santucci, G. M. Ghiggeri, and G. Candiano, "2DE maps in the discovery of human autoimmune kidney diseases: the case of membranous glomerulonephritis," Methods Mol Biol 1243, 127-138 (2015)

10) L. Santucci, M. Bruschi, G. M. Ghiggeri, and G. Candiano, "The latest advancements in proteomic two-dimensional gel electrophoresis analysis applied to biological samples," Methods Mol Biol 1243, 103-125 (2015)

11) Kiryluk K, Li Y, Scolari F, Sanna-Cherchi S, Choi M, Verbitsky M, Fasel D, Lata S, Prakash S, Shapiro S, Fischman C, Snyder HJ, Appel G, Izzi C, Viola BF, Dallera N, Del Vecchio L, Barlassina C, Salvi E, Bertinetto FE, Amoroso A, Savoldi S, Rocchietti M, Amore A, Peruzzi L, Coppo R, Salvadori M, Ravani P, Magistroni R, Ghiggeri GM, Caridi G, Bodria M, Lugani F, Allegri L, Delsante M, Maiorana M, Magnano A, Frasca G, Boer E, Boscutti G, Ponticelli C, Mignani R, Marcantoni C, Di Landro D, Santoro D, Pani A, Polci R, Feriozzi S, Chicca S, Galliani M, Gigante M, Gesualdo L, Zamboli P, Battaglia GG, Garozzo M, Maixnerová D, Tesar V, Eitner F, Rauen T, Floege J, Kovacs T, Nagy J, Mucha K, P?czek L, Zaniew M, Mizerska-Wasiak M, Roszkowska-Blaim M, Pawlaczyk K, Gale D, Barratt J, Thibaudin L, Berthoux F, Canaud G, Boland A, Metzger M, Panzer U, Suzuki H, Goto S, Narita I, Caliskan Y, Xie J, Hou P, Chen N, Zhang H, Wyatt RJ, Novak J, Julian BA, Feehally J, Stengel B, Cusi D, Lifton RP, Gharavi AG, “Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens” Nat Genet. 2014 Nov;46(11):1187-96. doi: 10.1038/ng.3118. Epub 2014 Oct 12.

12) Caridi G, Lugani F, Dagnino M, Gigante M, Iolascon A, Falco M, Graziano C, Benetti E, Dugo M, Del Prete D, Granata A, Borracelli D, Moggia E, Quaglia M, Rinaldi R, Gesualdo L, Ghiggeri GM, “Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy”Nephrol Dial Transplant.2014 Sep;29 Suppl 4:iv80-6. doi: 10.1093/ndt/gfu071.

13) Benetti E, Caridi G, Centi S, Vella MD, Ghiggeri GM, Artifoni L, Murer L, “mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis”,Saudi J Kidney Dis Transpl. 2014 Jul;25(4):854-7.

14) Quaglia M, Musetti C, Ghiggeri GM, Fogazzi GB, Settanni F, Boldorini RL, Lazzarich E, Airoldi A, Izzo C, Giordano M, Stratta P.Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy.Clin Transplant. 2014 Sep;28(9):995-1003. doi: 10.1111/ctr.12408. Epub 2014 Jul 18.

15)Westland R, Bodria M, Carrea A, Lata S, Scolari F, Fremeaux-Bacchi V, D’Agati VD, Lifton RP, Gharavi AG, Ghiggeri GM, Sanna-Cherchi S.Phenotypic expansion of DGKE-associated diseases.J Am Soc Nephrol. 2014 Jul;25(7):1408-14. doi: 10.1681/ASN.2013080886. Epub 2014 Feb 7.

16) Fallerini C, Dosa L, Tita R, Del Prete D, Feriozzi S, Gai G, Clementi M, La Manna A, Miglietti N, Mancini R, Mandrile G, Ghiggeri GM, Piaggio G, Brancati F, Diano L, Frate E, Pinciaroli AR, Giani M, Castorina P, Bresin E, Giachino D, De Marchi M, Mari F, Bruttini M, Renieri A, Ariani F, “Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases.Clin Genet. 2014 Sep;86(3):252-7. doi: 10.1111/cge.12258. Epub 2013 Oct 17.

17) Izzi C, Dallera N, Manenti C, Caridi G, Ghiggeri G, Rampoldi L, Scolari F.The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemia”.Kidney Int. 2014 Oct;86(4):863-4. doi: 10.1038/ki.2013.445.No abstract available.

18) Caridi G, Dagnino M, Erdeve O, Di Duca M, Yildiz D, Alan S, Atasay B, Arsan S, Campagnoli M, Galliano M, Minchiotti L. “Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene”.Biochem Med (Zagreb). 2014 Feb 15;24(1):151-8. doi: 10.11613/BM.2014.017. eCollection 2014

19) Lipska BS, Ranchin B, Iatropoulos P, Gellermann J, Melk A, Ozaltin F, Caridi G, Seeman T, Tory K, Jankauskiene A, Zurowska A, Szczepanska M, Wasilewska A, Harambat J, Trautmann A, Peco-Antic A, Borzecka H, Moczulska A, Saeed B, Bogdanovic R, Kalyoncu M, Simkova E, Erdogan O, Vrljicak K, Teixeira A, Azocar M, Schaefer F “Genotype-phenotype associations in WT1 glomerulopathy”; PodoNet Consortium.Kidney Int. 2014 May;85(5):1169-78. doi: 10.1038/ki.2013.519. Epub 2014 Jan

20) Nocera A, Cioni M, Tagliamacco A, Comoli P, Innocente A, Ceriolo P, Cardillo M, Ginevri F. “Serum complement inactivation unveiled prepregnancy donor-specific HLA antibodies leading to postpartum kidney graft loss” Transpl Int. 2015;28:623-5.

21) Tagliamacco A, Cioni M, Comoli P, Ramondetta M, Brambilla C, Trivelli A, Magnasco A, Biticchi R, Fontana I, Dulbecco P, Palombo D, Klersy C, Ghiggeri GM, Ginevri F, Cardillo M, Nocera A. “DQ molecules are the principal stimulators of de novo donor specific antibodies in non sensitized pediatric recipients receiving a first kidney transplant” Transpl Int. 2014 Mar 15.

22) Comoli P, Quartuccio G, Cioni M, Parodi A, Nocera A, Basso S, Fontana I, Magnasco A, Sioli V, Guido I, Klersy C, Zecca M, Cardillo M, Ghiggeri GM, Ginevri F. “Posttransplant Soluble B-Cell Activating Factor Kinetics in Pediatric Recipients of First Kidney Allograft”. Transplantation. 2015; 99:243-9).

23) Chesnaye N, Bonthuis M, Schaefer F, Groothoff JW, Verrina E, Heaf JG, Jankauskiene A, Lukosiene V, Molchanova EA, Mota C, Peco-Anti? A, Ratsch IM, Bjerre A, Roussinov DL, Sukalo A, Topaloglu R, Van Hoeck K, Zagozdzon I, Jager KJ, Van Stralen KJ; ESPN/ERA–EDTA registry.“Demographics of paediatric renal replacement therapy in Europe: a report of the ESPN/ERA-EDTA registry.” Pediatr Nephrol. 2014 Dec;29(12):2403-10. doi: 10.1007/s00467-014-2884-6.Epub 2014 Jul 21. PMID: 25039018

24)van Stralen KJ, Borzych-Du?alka D, Hataya H, Kennedy SE, Jager KJ, Verrina E, Inward C, Rönnholm K, Vondrak K, Warady BA, Zurowska AM, Schaefer F, Cochat P; ESPN/ERA-EDTA registry; IPPN registry; ANZDATA registry; Japanese RRT registry “Survival and clinical outcomes of children starting renal replacement therapy in the neonatal period”. Kidney Int. 2014 Jul;86(1):168-74. doi: 10.1038/ki.2013.561. Epub 2014 Feb 5. PMID: 24499775

25) Harambat J, van Stralen KJ, Verrina E, Groothoff JW, Schaefer F, Jager KJ; ESPN/ERA-EDTA Registry. “Likelihood of children with end-stage kidney disease in Europe to live with a functioning kidney transplant is mainly explained by nonmedical factors.” Pediatr Nephrol. 2014 Mar;29(3):453-9. PMID: 24232194

26) Harambat J, Bonthuis M, van Stralen KJ, Ariceta G, Battelino N, Bjerre A, Jahnukainen T, Leroy V, Reusz G, Sandes AR, Sinha MD, Groothoff JW, Combe C, Jager KJ, Verrina E, Schaefer F; ESPN/ERA-EDTA Registry. “Adult height in patients with advanced CKD requiring renal replacement therapy during childhood.” Clin J Am Soc Nephrol. 2014 Jan;9(1):92-9. doi: 10.2215/CJN.00890113. Epub 2013 Oct 31.PMID: 24178977

27)Bonthuis M, van Stralen KJ, Jager KJ, Baiko S, Jahnukainen T, Laube GF, Podracka L, Seeman T, Tyerman K, Ulinski T, Groothoff JW, Schaefer F, Verrina E. “Dyslipidaemia in children on renal replacement therapy.” Nephrol Dial Transplant. 2014 Mar;29(3):594-603. doi: 10.1093/ndt/gft429. Epub 2013 Oct 29. PMID: 24170813

28) Di Zazzo G, Guzzo I, De Galasso L, Fortunato M, Leozappa G, Peruzzi L, Vidal E, Corrado C,Verrina E, Picca S, Emma F. “Anterior ischemic optical neuropathy in children on chronic peritoneal dialysis: report of 7 cases.”Perit Dial Int. 2015 in press

29) Ha IS, Yap HK, Munarriz RL, Zambrano PH, Flynn JT, Bilge I, Szczepanska M, Lai WM, Antonio ZL, Gulati A, Hooman N, van Hoeck K, Higuita LM, Verrina E, Klaus G, Fischbach M, Riyami MA, Sahpazova E, Sander A, Warady BA, Schaefer F. “Risk factors for loss of residual renal function in children treated with chronic peritoneal dialysis.”Kidney Int. 2015 in press

30) Bonthuis M, Busutti M, van Stralen KJ, Jager KJ, Baiko S, Bakkalo?lu S, Battelino N, Gaydarova M, Gianoglio B, Parvex P, Gomes C, Heaf JG, Podracka L, Kuzmanovska D, Molchanova MS, Pankratenko TE, Papachristou F, Reusz G, Sanahuja MJ, Shroff R, Groothoff JW, Schaefer F,Verrina E. “Mineral metabolism in European children living with a renal transplant: a European society for paediatric nephrology/european renal association-European dialysis and transplant association registry study.”Clin J Am Soc Nephrol. 2015 in press

31) Sanchez-Montanez A, Morana G, Mancardi MM, Janis S, Severino M, Verrina E, Rossi A. “Reversible cerebral vasoconstriction mimicking posterior reversible encephalopathy syndrome in an infant with end-stage renal disease.”Cephalalgia. 2015 in press

32) Picca S, Dionisi-Vici C, Bartuli A, De Palo T, Papadia F, Montini G, Materassi M, Donati MA, VerrinaE, Schiaffino MC, Pecoraro C, Iaccarino E, Vidal E, Burlina A, Emma F. “Short-term survival of hyperammonemic neonates treated with dialysis.”Pediatr Nephrol. 2015 in press 

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