| The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis V Palazzo, A Provenzano, F Becherucci, G Sansavini, B Mazzinghi, ... Kidney international 91 (5), 1243-1255, 2017 | 109 | 2017 |
| Atopy in childhood idiopathic nephrotic syndrome ME Salsano, L Graziano, I Luongo, P Pilla, M Giordano, G Lama Acta paediatrica 96 (4), 561-566, 2007 | 62 | 2007 |
| Clinical experience with darbepoietin alfa (NESP) in children undergoing hemodialysis T De Palo, M Giordano, F Palumbo, R Bellantuono, G Messina, V Colella, ... Pediatric Nephrology 19, 337-340, 2004 | 58 | 2004 |
| Voiding urosonography as first step in the diagnosis of vesicoureteral reflux in children: a clinical experience M Giordano, R Marzolla, F Puteo, L Scianaro, DA Caringella, T Depalo Pediatric radiology 37, 674-677, 2007 | 50 | 2007 |
| Community-wide outbreak of haemolytic uraemic syndrome associated with Shiga toxin 2-producing Escherichia coli O26: H11 in southern Italy, summer 2013 C Germinario, A Caprioli, M Giordano, M Chironna, MS Gallone, S Tafuri, ... Eurosurveillance 21 (38), 30343, 2016 | 48 | 2016 |
| Indications and results of renal biopsy in children: a 36-year experience L Santangelo, GS Netti, P Giordano, V Carbone, M Martino, DD Torres, ... World Journal of Pediatrics 14, 127-133, 2018 | 44 | 2018 |
| A novel SMARCAL1 mutation associated with a mild phenotype of Schimke immuno-osseous dysplasia (SIOD) L Santangelo, M Gigante, GS Netti, S Diella, F Puteo, V Carbone, ... BMC nephrology 15, 1-5, 2014 | 43 | 2014 |
| Expanding the mutation spectrum in 130 probands with ARPKD: identification of 62 novel PKHD1 mutations by sanger sequencing and MLPA analysis S Melchionda, T Palladino, S Castellana, M Giordano, E Benetti, ... Journal of human genetics 61 (9), 811-821, 2016 | 37 | 2016 |
| Continuous kidney replacement therapy in critically ill neonates and infants: a retrospective analysis of clinical results with a dedicated device F Garzotto, E Vidal, Z Ricci, F Paglialonga, M Giordano, N Laforgia, ... Pediatric Nephrology 35, 1699-1705, 2020 | 36 | 2020 |
| Preservation of renal function in atypical hemolytic uremic syndrome by eculizumab: a case report M Giordano, G Castellano, G Messina, C Divella, R Bellantuono, F Puteo, ... Pediatrics 130 (5), e1385-e1388, 2012 | 36 | 2012 |
| Impact of COVID-19 pandemic in children with CKD or immunosuppression A Mastrangelo, W Morello, E Vidal, I Guzzo, LA Petruzzelli, E Benetti, ... Clinical Journal of the American Society of Nephrology 16 (3), 449-451, 2021 | 35 | 2021 |
| A pediatric neurologic assessment score may drive the eculizumab-based treatment of Escherichia coli-related hemolytic uremic syndrome with neurological … P Giordano, GS Netti, L Santangelo, G Castellano, V Carbone, DD Torres, ... Pediatric Nephrology 34, 517-527, 2019 | 34 | 2019 |
| Mutational Spectrum of CYP24A1 Gene in a Cohort of Italian Patients with Idiopathic Infantile Hypercalcemia M Gigante, L Santangelo, S Diella, G Caridi, L Argentiero, ... Nephron 133 (3), 193-204, 2016 | 34 | 2016 |
| Further phenotypic heterogeneity of CoQ10 deficiency associated with steroid resistant nephrotic syndrome and novel COQ2 and COQ6 variants. M Gigante, S Diella, L Santangelo, E Trevisson, MJ Acosta, M Amatruda, ... Clinical Genetics 2 (92), 224-226, 2017 | 28 | 2017 |
| Survival of infants treated with CKRT: comparing adapted adult platforms with the Carpediem™ SL Goldstein, E Vidal, Z Ricci, F Paglialonga, L Peruzzi, M Giordano, ... Pediatric Nephrology 37 (3), 667-675, 2022 | 27 | 2022 |
| Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies L Gianesello, M Ceol, L Bertoldi, L Terrin, G Priante, L Murer, L Peruzzi, ... International Journal of Molecular Sciences 21 (2), 516, 2020 | 27 | 2020 |
| ADPedKD: a global online platform on the management of children with ADPKD S De Rechter, D Bockenhauer, LM Guay-Woodford, I Liu, AJ Mallett, ... Kidney international reports 4 (9), 1271-1284, 2019 | 23 | 2019 |
| Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia? M Morimoto, C Myung, K Beirnes, K Choi, Y Asakura, A Bokenkamp, ... Orphanet journal of rare diseases 11, 1-12, 2016 | 22 | 2016 |
| Novel mutations of the CLCN5 gene including a complex allele and A 5′ UTR mutation in Dent disease 1. E Tosetto, M Ceol, F Mezzabotta, A Ammenti, L Peruzzi, MR Caruso, ... Clinical genetics 76 (4), 2009 | 20 | 2009 |
| Therapeutic apheresis in children: experience in a pediatric dialysis center T De Palo, M Giordano, R Bellantuono, V Colella, D Troise, F Palumbo, ... The International Journal of Artificial Organs 23 (12), 834-839, 2000 | 20 | 2000 |
Loreto GesualdoProfessore Ordinario di NefrologiaVerified email at uniba.it
