Fondo malattie renali del bambino - Fondazione malattie renali del bambino
Pubblicazioni 2018
Fondo Malattie Renali del Bambino - Fondazione Malattie Renali del Bambino - Istituto Gaslini Genova

Pubblicazioni 2018

Con la partecipazione attiva della nostra Fondazione

  1. Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, Mitrotti A, Fasel DA, Batourina E, Sampson MG, Bodria M, Werth M, Kao C, Martino J, Capone VP, Vivante A, Shril S, Kil BH, Marasà M, Zhang JY, Na YJ, Lim TY, Ahram D, Weng PL, Heinzen EL, Carrea A, Piaggio G, Gesualdo L, Manca V, Masnata G, Gigante M, Cusi D, Izzi C, Scolari F, van Wijk JAE, Saraga M, Santoro D, Conti G, Zamboli P, White H, Drozdz D, Zachwieja K, Miklaszewska M, Tkaczyk M, Tomczyk D, Krakowska A, Sikora P, Jarmolinski T, Borszewska-Kornacka MK, Pawluch R, Szczepanska M, Adamczyk P, Mizerska-Wasiak M, Krzemien G, Szmigielska A, Zaniew M, Dobson MG, Darlow JM, Puri P, Barton DE, Furth SL, Warady BA, Gucev Z, Lozanovski VJ, Tasic V, Pisani I, Allegri L, Rodas LM, Campistol JM, Jeanpierre C, Alam S, Casale P, Wong CS, Lin F, Miranda DM, Oliveira EA, Simões-E-Silva AC, Barasch JM, Levy B, Wu N, Hildebrandt F, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Zhang F, Hakonarson H, Papaioannou VE, Mendelsohn CL, Gharavi AG, Sanna-Cherchi S.
    The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
    Nat Genet. 2019 Jan;51(1):117-127. doi: 10.1038/s41588-018-0281-y. Epub 2018 Dec 21.
  2. Wong MCY, Sertorio F, Damasio MB, Incarbone V, Beati F, Bodria M, Pistorio A, Ghiggeri GM, Magnano GM, Mattioli G.
    Surgical validation of functional magnetic resonance urography in the study of ureteropelvic junction obstruction in a pediatric cohort.
    J Pediatr Urol. 2018 Nov 22. pii: S1477-5131(18)30678-8. doi: 10.1016/j.jpurol.2018.11.008. [Epub ahead of print]
  3. Selewski DT, Ambruzs JM, Appel GB, Bomback AS, Matar RB, Cai Y, Cattran DC, Chishti AS, D’Agati VD, D’Alessandri-Silva CJ, Gbadegesin RA, Hogan JJ, Iragorri S, Jennette JC, Julian BA, Khalid M, Lafayette RA, Liapis H, Lugani F, Mansfield SA, Mason S, Nachman PH, Nast CC, Nester CM, Noone DG, Novak J, O’Shaughnessy MM, Reich HN, Rheault MN, Rizk DV, Saha MK, Sanghani NS, Sperati CJ, Sreedharan R, Srivastava T, Swiatecka-Urban A, Twombley K, Vasylyeva TL, Weaver DJ, Yin H, Zee J, Falk RJ, Gharavi AG, Gillespie BW, Gipson DS, Greenbaum LA, Holzman LB, Kretzler M, Robinson BM, Smoyer WE, Flessner M, Guay-Woodford LM, Kiryluk K; CureGN Consortium.
    Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study.
    Kidney Int Rep. 2018 Aug 3;3(6):1373-1384. doi: 10.1016/j.ekir.2018.07.021. eCollection 2018 Nov.
  4. Mariani LH, Bomback AS, Canetta PA, Flessner MF, Helmuth M, Hladunewich MA, Hogan JJ, Kiryluk K, Nachman PH, Nast CC, Rheault MN, Rizk DV, Trachtman H, Wenderfer SE, Bowers C, Hill-Callahan P, Marasa M, Poulton CJ, Revell A, Vento S, Barisoni L, Cattran D, D’Agati V, Jennette JC, Klein JB, Laurin LP, Twombley K, Falk RJ, Gharavi AG, Gillespie BW, Gipson DS, Greenbaum LA, Holzman LB, Kretzler M, Robinson B, Smoyer WE, Guay-Woodford LM; CureGN Consortium.
    CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular Disease.
    Am J Kidney Dis. 2018 Nov 9. pii: S0272-6386(18)30936-3. doi: 10.1053/j.ajkd.2018.07.020. [Epub ahead of print]
  5. Nuovo S, Fuiano L, Micalizzi A, Battini R, Bertini E, Borgatti R, Caridi G, D’Arrigo S, Fazzi E, Fischetto R, Ghiggeri GM, Giordano L, Leuzzi V, Romaniello R, Signorini S, Stringini G, Zanni G, Romani M, Valente EM, Emma F.
    Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome.
    Nephrol Dial Transplant. 2018 Nov 6. doi: 10.1093/ndt/gfy333. [Epub ahead of print]
  6. Panfoli I, Santucci L, Bruschi M, Petretto A, Calzia D, Ramenghi LA, Ghiggeri G, Candiano G.
    Microvesicles as promising biological tools for diagnosis and therapy.
    Expert Rev Proteomics. 2018 Oct;15(10):801-808. doi: 10.1080/14789450.2018.1528149. Epub 2018 Oct 4.
  7. Cioni M, Nocera A, Tagliamacco A, Basso S, Innocente A, Fontana I, Magnasco A, Trivelli A, Klersy C, Gurrado A, Ramondetta M, Boghen S, Catenacci L, Verrina E, Garibotto G, Ghiggeri GM, Cardillo M, Ginevri F, Comoli P.
    Failure to remove de novo donor-specific HLA antibodies is influenced by antibody properties and identifies kidney recipients with late antibody-mediated rejection destined to graft loss - a retrospective study.
    Transpl Int. 2019 Jan;32(1):38-48. doi: 10.1111/tri.13325. Epub 2018 Aug 27.
  8. Vaglio A, Grayson PC, Fenaroli P, Gianfreda D, Boccaletti V, Ghiggeri GM, Moroni G.
    Drug-induced lupus: Traditional and new concepts.
    Autoimmun Rev. 2018 Sep;17(9):912-918. doi: 10.1016/j.autrev.2018.03.016. Epub 2018 Jul 10. Review.
  9. Bertelli R, Bonanni A, Caridi G, Canepa A, Ghiggeri GM.
    Molecular and Cellular Mechanisms for Proteinuria in Minimal Change Disease.
    Front Med (Lausanne). 2018 Jun 11;5:170. doi: 10.3389/fmed.2018.00170. eCollection 2018. Review.
  10. Bruschi M, Petretto A, Vaglio A, Santucci L, Candiano G, Ghiggeri GM.
    Annexin A1 and Autoimmunity: From Basic Science to Clinical Applications.
    Int J Mol Sci. 2018 May 3;19(5). pii: E1348. doi: 10.3390/ijms19051348. Review.
  11. Bonanni A, Calatroni M, D’Alessandro M, Signa S, Bertelli E, Cioni M, Di Marco E, Biassoni R, Caridi G, Ingrasciotta G, Bertelli R, Di Donato A, Bruschi M, Canepa A, Piaggio G, Ravani P, Ghiggeri GM.
    Adverse events linked with the use of chimeric and humanized anti-CD20 antibodies in children with idiopathic nephrotic syndrome.
    Br J Clin Pharmacol. 2018 Jun;84(6):1238-1249. doi: 10.1111/bcp.13548. Epub 2018 Mar 25.
  12. Bruschi M, Petretto A, Caicci F, Bartolucci M, Calzia D, Santucci L, Manni L, Ramenghi LA, Ghiggeri G, Traverso CE, Candiano G, Panfoli I.
    Proteome of Bovine Mitochondria and Rod Outer Segment Disks: Commonalities and Differences.
    J Proteome Res. 2018 Feb 2;17(2):918-925. doi: 10.1021/acs.jproteome.7b00741. Epub 2018 Jan 18.
  13. Calzia D., Degan P., Caicci F., Bruschi M., Manni L., Ramenghi L.A., Candiano G., Traverso C.E., Panfoli I.,
    Modulation of the rod outer segment aerobic metabolism diminishes the production of radicals due to light absorption
    Free Radic Biol Med 117 (2018) 110-118.
  14. Gaggero S., Bruschi M., Petretto A., Parodi M., Zotto G.D., Lavarello C., Prato C., Santucci L., Barbuto A., Bottino C., Candiano G., Moretta A., Vitale M., Moretta L., Cantoni C.,
    Nidogen-1 is a novel extracellular ligand for the NKp44 activating receptor
    Oncoimmunology 7(9) (2018) e1470730.
  15. Sanna-Cherchi S, Westland R, Ghiggeri GM, Gharavi AG.
    Genetic basis of human congenital anomalies of the kidney and urinary tract.
    J Clin Invest. 2018 Jan 2;128(1):4-15. doi: 10.1172/JCI95300. Epub 2018 Jan 2. Review.
  16. Sanna-Cherchi S, Khan K, Westland R, Krithivasan P, Fievet L, Rasouly HM, Ionita-Laza I, Capone VP, Fasel DA, Kiryluk K, Kamalakaran S, Bodria M, Otto EA, Sampson MG, Gillies CE, Vega-Warner V, Vukojevic K, Pediaditakis I, Makar GS, Mitrotti A, Verbitsky M, Martino J, Liu Q, Na YJ, Goj V, Ardissino G, Gigante M, Gesualdo L, Janezcko M, Zaniew M, Mendelsohn CL, Shril S, Hildebrandt F, van Wijk JAE, Arapovic A, Saraga M, Allegri L, Izzi C, Scolari F, Tasic V, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Mane S, Goldstein DB, Lifton RP, Katsanis N, Davis EE, Gharavi AG.
    Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
    Am J Hum Genet. 2017 Dec 7;101(6):1034. doi: 10.1016/j.ajhg.2017.11.003. No abstract available.
  17. Doublier S, Zennaro C, Musante L, Spatola T, Candiano G, Bruschi M, Besso L, Cedrino M, Carraro M, Ghiggeri GM, Camussi G, Lupia E.
    Soluble CD40 ligand directly alters glomerular permeability and may act as a circulating permeability factor in FSGS.
    PLoS One. 2017 Nov 20;12(11):e0188045. doi: 10.1371/journal.pone.0188045. eCollection 2017.
  18. Rossi GM, Bonatti F, Adorni A, Alberici F, Bodria M, Bonanni A, Ghiggeri GM, Martorana D, Vaglio A.
    FCGR2A single nucleotide polymorphism confers susceptibility to childhood-onset idiopathic nephrotic syndrome.
    Immunol Lett. 2018 Jan;193:11-13. doi: 10.1016/j.imlet.2017.11.002. Epub 2017 Nov 15.
  19. Bruschi M, Santucci L, Ravera S, Bartolucci M, Petretto A, Calzia D, Ghiggeri GM, Ramenghi LA, Candiano G, Panfoli I.
    Metabolic Signature of Microvesicles from Umbilical Cord Mesenchymal Stem Cells of Preterm and Term Infants.
    Proteomics Clin Appl. 2018 May;12(3):e1700082. doi: 10.1002/prca.201700082. Epub 2017 Dec 5.
  20. Wong MCY, Piaggio G, Damasio MB, Molinelli C, Ferretti SM, Pistorio A, Ghiggeri G, Degl’Innocenti ML, Canepa A, Incarbone V, Mattioli G.
    Hydronephrosis and crossing vessels in children: Optimization of diagnostic-therapeutic pathway and analysis of color Doppler ultrasound and magnetic resonance urography diagnostic accuracy.
    J Pediatr Urol. 2018 Feb;14(1):68.e1-68.e6. doi: 10.1016/j.jpurol.2017.09.019. Epub 2017 Oct 27.
  21. Sanna-Cherchi S, Khan K, Westland R, Krithivasan P, Fievet L, Rasouly HM, Ionita-Laza I, Capone VP, Fasel DA, Kiryluk K, Kamalakaran S, Bodria M, Otto EA, Sampson MG, Gillies CE, Vega-Warner V, Vukojevic K, Pediaditakis I, Makar GS, Mitrotti A, Verbitsky M, Martino J, Liu Q, Na YJ, Goj V, Ardissino G, Gigante M, Gesualdo L, Janezcko M, Zaniew M, Mendelsohn CL, Shril S, Hildebrandt F, van Wijk JAE, Arapovic A, Saraga M, Allegri L, Izzi C, Scolari F, Tasic V, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Mane S, Goldstein DB, Lifton RP, Katsanis N, Davis EE, Gharavi AG.
    Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
    Am J Hum Genet. 2017 Nov 2;101(5):789-802. doi: 10.1016/j.ajhg.2017.09.018. Erratum in: Am J Hum Genet. 2017 Dec 7;101(6):1034.
  22. Radice A, Pieruzzi F, Trezzi B, Ghiggeri G, Napodano P, D’Amico M, Stellato T, Brugnano R, Ravera F, Rolla D, Pesce G, Giovenzana ME, Londrino F, Cantaluppi V, Pregnolato F, Volpi A, Rombolà G, Moroni G, Ortisi G, Sinico RA.
    Diagnostic specificity of autoantibodies to M-type phospholipase A2 receptor (PLA2R) in differentiating idiopathic membranous nephropathy (IMN) from secondary forms and other glomerular diseases.
    J Nephrol. 2018 Apr;31(2):271-278. doi: 10.1007/s40620-017-0451-5. Epub 2017 Oct 28.
  23. Dufek S, Ylinen E, Trautmann A, Alpay H, Ariceta G, Aufricht C, Bacchetta J, Bakkaloglu S, Bayazit A, Caliskan S, do Sameiro Faria M, Dursun I, Ekim M, Jankauskiene A, Klaus G, Paglialonga F, Pasini A, Printza N, Conti VS, Schmitt CP, Stefanidis C, Verrina E, Vidal E, Webb H, Zampetoglou A, Edefonti A, Holtta T, Shroff R; ESPN Dialysis Working Group.
    Infants with congenital nephrotic syndrome have comparable outcomes to infants with other renal diseases.
    Pediatr Nephrol. 2018 Oct 29. doi: 10.1007/s00467-018-4122-0. [Epub ahead of print]
  24. Dufek S, Holtta T, Trautmann A, Ylinen E, Alpay H, Ariceta G, Aufricht C, Bacchetta J, Bakkaloglu SA, Bayazit A, Cicek RY, Dursun I, Duzova A, Ekim M, Iancu D, Jankauskiene A, Klaus G, Paglialonga F, Pasini A, Printza N, Said Conti V, do Sameiro Faria M, Schmitt CP, Stefanidis CJ, Verrina E, Vidal E, Vondrak K, Webb H, Zampetoglou A, Bockenhauer D, Edefonti A, Shroff R.
    Management of children with congenital nephrotic syndrome: challenging treatment paradigms.
    Nephrol Dial Transplant. 2018 Jun 21. doi: 10.1093/ndt/gfy165. [Epub ahead of print]
  25. Willem L, Knops N, Mekahli D, Cochat P, Edefonti A, Verrina E, Groothoff J, Lagae L, Pirenne J, Dobbels F, Borry P, Van Geet C, Levtchenko E.
    Renal Replacement Therapy in children with severe developmental disability: guiding questions for decision-making.
    Eur J Pediatr. 2018 Dec;177(12):1735-1743. doi: 10.1007/s00431-018-3238-3. Epub 2018 Sep 7.
  26. Vidal E, Alberici I, Verrina E; Italian Registry of Pediatric Chronic Dialysis.
    Acute pancreatitis in children on chronic maintenance dialysis.
    Pediatr Nephrol. 2018 Aug 23. doi: 10.1007/s00467-018-4043-y. [Epub ahead of print]
  27. d’Annunzio G, Beccaria A, Pistorio A, Verrina E, Minuto N, Pontremoli R, La Valle A, Maghnie M.
    Predictors of renal complications in pediatric patients with type 1 diabetes mellitus: A prospective cohort study.
    J Diabetes Complications. 2018 Oct;32(10):955-960. doi: 10.1016/j.jdiacomp.2018.02.007. Epub 2018 Aug 11.
  28. Cioni M, Nocera A, Tagliamacco A, Basso S, Innocente A, Fontana I, Magnasco A, Trivelli A, Klersy C, Gurrado A, Ramondetta M, Boghen S, Catenacci L, Verrina E, Garibotto G, Ghiggeri GM, Cardillo M, Ginevri F, Comoli P.
    Failure to remove de novo donor-specific HLA antibodies is influenced by antibody properties and identifies kidney recipients with late antibody-mediated rejection destined to graft loss - a retrospective study.
    Transpl Int. 2019 Jan;32(1):38-48. doi: 10.1111/tri.13325. Epub 2018 Aug 27.
  29. Severino M, Giacomini T, Verrina E, Prato G, Rossi A.
    Reversible cerebral vasoconstriction complicating cerebral atherosclerotic vascular disease in Schimke immuno-osseous dysplasia.
    Neuroradiology. 2018 Sep;60(9):885-888. doi: 10.1007/s00234-018-2052-y. Epub 2018 Jul 6. No abstract available.
  30. Schaefer B, Bartosova M, Macher-Goeppinger S, Sallay P, Vörös P, Ranchin B, Vondrak K, Ariceta G, Zaloszyc A, Bayazit AK, Querfeld U, Cerkauskiene R, Testa S, Taylan C, VandeWalle J, Yap Y, Krmar RT, Büscher R, Mühlig AK, Drozdz D, Caliskan S, Lasitschka F, Fathallah-Shaykh S, Verrina E, Klaus G, Arbeiter K, Bhayadia R, Melk A, Romero P, Warady BA, Schaefer F, Ujszaszi A, Schmitt CP.
    Neutral pH and low-glucose degradation product dialysis fluids induce major early alterations of the peritoneal membrane in children on peritoneal dialysis.
    Kidney Int. 2018 Aug;94(2):419-429. doi: 10.1016/j.kint.2018.02.022.
  31. Lerch C, Shroff R, Wan M, Rees L, Aitkenhead H, Kaplan Bulut I, Thurn D, Karabay Bayazit A, Niemirska A, Canpolat N, Duzova A, Azukaitis K, Yilmaz E, Yalcinkaya F, Harambat J, Kiyak A, Alpay H, Habbig S, Zaloszyc A, Soylemezoglu O, Candan C, Rosales A, Melk A, Querfeld U, Leifheit-Nestler M, Sander A, Schaefer F, Haffner D; 4C study consortium ; ESPN CKD-MBD working group .
    Effects of nutritional vitamin D supplementation on markers of bone and mineral metabolism in children with chronic kidney disease.
    Nephrol Dial Transplant. 2018 Dec 1;33(12):2208-2217. doi: 10.1093/ndt/gfy012.
  32. Van Stralen KJ, Verrina E, Belingheri M, Dudley J, Dušek J, Grenda R, Macher MA, Puretic Z, Rubic J, Rudaitis S, Rudin C, Schaefer F, Jager KJ; ESPN/ERA-EDTA Registry.
    Impact of graft loss among kidney diseases with a high risk of post-transplant recurrence in the paediatric population.
    Nephrol Dial Transplant. 2018 Mar 1;33(3):542. doi: 10.1093/ndt/gfx372. No abstract available.
  33. Bakkaloglu SA, Özdemir Atikel Y, Paglialonga F, Stefanidis CJ, Askiti V, Vidal E, Ariceta G, Melek E, Verrina E, Printza N, Vondrak K, Zurowska A, Zagozdzon I, Ekim M, Özmert EN, Dufek S, Jankauskiene A, Schmitt CP, Lévai E, Vande Walle J, Canpolat N, Holtta T, Fischbach M, Klaus G, Aufricht C, Shroff R, Edefonti A.
    Vaccination Practices in Pediatric Dialysis Patients Across Europe. A European Pediatric Dialysis Working Group and European Society for Pediatric Nephrology Dialysis Working Group Study.
    Nephron. 2018;138(4):280-286. doi: 10.1159/000485398. Epub 2017 Dec 12.
  34. Vidal E, Chesnaye NC, Paglialonga F, Minale B, Leozappa G, Giordano M, Gianoglio B, Corrado C, Roperto RM, Chimenz R, Mencarelli F, Ratsch IM, Murer L, Verrina E; Italian Registry for Paediatric Chronic Dialysis.
    A propensity-matched comparison of hard outcomes in children on chronic dialysis.
    Eur J Pediatr. 2018 Jan;177(1):117-124. doi: 10.1007/s00431-017-3040-7. Epub 2017 Nov 16.
  35. Yalcinkaya F, Bonthuis M, Erdogan BD, van Stralen KJ, Baiko S, Chehade H, Maxwell H, Montini G, Rönnholm K, Sørensen SS, Ulinski T, Verrina E, Weber S, Harambat J, Schaefer F, Jager KJ, Groothoff JW.
    Outcomes of renal replacement therapy in boys with prune belly syndrome: findings from the ESPN/ERA-EDTA Registry.
    Pediatr Nephrol. 2018 Jan;33(1):117-124. doi: 10.1007/s00467-017-3770-9. Epub 2017 Aug 4.

 

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