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Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
Brioude F, Kalish JM, Mussa A, Foster AC, Bliek J, Ferrero GB, Boonen SE, Cole T, Baker R, Bertoletti M, Cocchi G, Coze C, De Pellegrin M, Hussain K, Ibrahim A, Kilby MD, Krajewska-Walasek M, Kratz CP, Ladusans EJ, Lapunzina P, Le Bouc Y, Maas SM, Macdonald F, Õunap K, Peruzzi L, Rossignol S, Russo S, Shipster C, Skórka A, Tatton-Brown K, Tenorio J, Tortora C, Grønskov K, Netchine I, Hennekam RC, Prawitt D, Tümer Z, Eggermann T, Mackay DJG, Riccio A, Maher ER. Brioude F, et al. Among authors: peruzzi l. Nat Rev Endocrinol. 2018 Apr;14(4):229-249. doi: 10.1038/nrendo.2017.166. Epub 2018 Jan 29. Nat Rev Endocrinol. 2018. PMID: 29377879 Free PMC article. Review.
Vascular access in children requiring maintenance haemodialysis: a consensus document by the European Society for Paediatric Nephrology Dialysis Working Group.
Shroff R, Calder F, Bakkaloğlu S, Nagler EV, Stuart S, Stronach L, Schmitt CP, Heckert KH, Bourquelot P, Wagner AM, Paglialonga F, Mitra S, Stefanidis CJ; European Society for Paediatric Nephrology Dialysis Working Group. Shroff R, et al. Nephrol Dial Transplant. 2019 Oct 1;34(10):1746-1765. doi: 10.1093/ndt/gfz011. Nephrol Dial Transplant. 2019. PMID: 30859187
Functional analysis of BMP4 mutations identified in pediatric CAKUT patients.
Tabatabaeifar M, Schlingmann KP, Litwin M, Emre S, Bakkaloglu A, Mehls O, Antignac C, Schaefer F, Weber S; ESCAPE Trial Group. Tabatabaeifar M, et al. Pediatr Nephrol. 2009 Dec;24(12):2361-8. doi: 10.1007/s00467-009-1287-6. Epub 2009 Aug 14. Pediatr Nephrol. 2009. PMID: 19685083
Impact of COVID-19 Pandemic in Children with CKD or Immunosuppression.
Mastrangelo A, Morello W, Vidal E, Guzzo I, Annicchiarico Petruzzelli L, Benetti E, Materassi M, Giordano M, Pasini A, Corrado C, Puccio G, Chimenz R, Pecoraro C, Massella L, Peruzzi L, Montini G; COVID-19 Task Force of the Italian Society of Pediatric Nephrology; COVID-19 TASK FORCE of the Italian Society of Pediatric Nephrology. Mastrangelo A, et al. Among authors: peruzzi l. Clin J Am Soc Nephrol. 2021 Mar 8;16(3):449-451. doi: 10.2215/CJN.13120820. Epub 2020 Dec 14. Clin J Am Soc Nephrol. 2021. PMID: 33318026 Free PMC article. No abstract available.
Prevalence of SARS-CoV-2-IgG Antibodies in Children with CKD or Immunosuppression.
Morello W, Mastrangelo A, Guzzo I, Cusinato L, Annicchiarico Petruzzelli L, Benevenuta C, Martelli L, Dall'Amico R, Vianello FA, Puccio G, Massella L, Benetti E, Pecoraro C, Peruzzi L, Montini G; COVID-19 Task Force of the Italian Society of Pediatric Nephrology. Morello W, et al. Among authors: peruzzi l. Clin J Am Soc Nephrol. 2021 Jul;16(7):1097-1099. doi: 10.2215/CJN.00330121. Epub 2021 Jun 7. Clin J Am Soc Nephrol. 2021. PMID: 34099499 Free PMC article. No abstract available.
Longitudinal evaluation of mycophenolic acid pharmacokinetics in pediatric kidney transplant recipients. The role of post-transplant clinical and therapeutic variables.
Ghio L, Ferraresso M, Zacchello G, Murer L, Ginevri F, Belingheri M, Peruzzi L, Zanon F, Perfumo F, Berardinelli L, Tirelli S, Dello Strologo L, Fontana I, Valente U, Cardillo M, Edefonti A. Ghio L, et al. Among authors: peruzzi l. Clin Transplant. 2009 Mar-Apr;23(2):264-70. doi: 10.1111/j.1399-0012.2008.00932.x. Epub 2009 Dec 18. Clin Transplant. 2009. PMID: 19191807
The frequency of rare and monogenic diseases in pediatric organ transplant recipients in Italy.
Vaisitti T, Peritore D, Magistroni P, Ricci A, Lombardini L, Gringeri E, Catalano S, Spada M, Sciveres M, Di Giorgio A, Limongelli G, Varrenti M, Gerosa G, Terzi A, Pace Napoleone C, Amodeo A, Ragni L, Dello Strologo L, Benetti E, Fontana I, Testa S, Peruzzi L, Mitrotti A, Abbate S, Comai G, Gotti E, Schiavon M, Boffini M, De Angelis D, Bertani A, Pinelli D, Torre M, Poggi C, Deaglio S, Cardillo M, Amoroso A; Italian Pediatric Transplant Centers. Vaisitti T, et al. Among authors: peruzzi l. Orphanet J Rare Dis. 2021 Sep 4;16(1):374. doi: 10.1186/s13023-021-02013-x. Orphanet J Rare Dis. 2021. PMID: 34481500 Free PMC article.
249 results