Artikel dengan mandat akses publik - Elisa BenettiPelajari lebih lanjut
Tidak tersedia di mana pun: 2
C5 convertase blockade in membranoproliferative glomerulonephritis: a single-arm clinical trial
P Ruggenenti, E Daina, A Gennarini, C Carrara, S Gamba, M Noris, ...
American Journal of Kidney Diseases 74 (2), 224-238, 2019
Mandat: Government of Italy
Kidney versus combined kidney and liver transplantation in young people with autosomal recessive polycystic kidney disease: data from the European Society for Pediatric …
D Mekahli, KJ van Stralen, M Bonthuis, KJ Jager, A Balat, E Benetti, ...
American Journal of Kidney Diseases 68 (5), 782-788, 2016
Mandat: US National Institutes of Health
Tersedia di suatu tempat: 10
Genetic screening in adolescents with steroid-resistant nephrotic syndrome
BS Lipska, P Iatropoulos, R Maranta, G Caridi, F Ozaltin, A Anarat, A Balat, ...
Kidney international 84 (1), 206-213, 2013
Mandat: German Research Foundation
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract
S Gimelli, G Caridi, S Beri, K McCracken, R Bocciardi, P Zordan, ...
Human mutation 31 (12), 1352-1359, 2010
Mandat: Fondazione Telethon, Italy
Molecular and clinical characterization of patients with overlapping 10p deletions
A Lindstrand, H Malmgren, A Verri, E Benetti, M Eriksson, A Nordgren, ...
American journal of medical genetics Part A 152 (5), 1233-1243, 2010
Mandat: Swedish Research Council
Deciphering variability of PKD1 and PKD2 in an Italian cohort of 643 patients with autosomal dominant polycystic kidney disease (ADPKD)
P Carrera, S Calzavara, R Magistroni, JT Den Dunnen, F Rigo, S Stenirri, ...
Scientific reports 6 (1), 30850, 2016
Mandat: Government of Italy
Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy
G Caridi, F Lugani, M Dagnino, M Gigante, A Iolascon, M Falco, ...
Nephrology Dialysis Transplantation 29 (suppl_4), iv80-iv86, 2014
Mandat: Government of Italy
Outcome of childhood-onset full-house nephropathy
B Ruggiero, M Vivarelli, A Gianviti, C Pecoraro, L Peruzzi, E Benetti, ...
Nephrology Dialysis Transplantation 32 (7), 1194-1204, 2017
Mandat: Government of Italy
Results of the PROPINE randomized controlled study suggest tapering of prednisone treatment for relapses of steroid sensitive nephrotic syndrome is not necessary in children
A Gargiulo, L Massella, B Ruggiero, L Ravà, MC Degli Atti, M Materassi, ...
Kidney International 99 (2), 475-483, 2021
Mandat: Government of Italy
The frequency of rare and monogenic diseases in pediatric organ transplant recipients in Italy
T Vaisitti, D Peritore, P Magistroni, A Ricci, L Lombardini, E Gringeri, ...
Orphanet Journal of Rare Diseases 16, 1-17, 2021
Mandat: Government of Italy
Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria
A Pelle, A Cuccurullo, C Mancini, R Sebastiano, G Stallone, S Negrisolo, ...
Journal of Nephrology 30, 219-225, 2017
Mandat: Fondazione Telethon, Italy
Functional study of novel Bartter’s syndrome mutations in ClC-Kb and rescue by the accessory subunit barttin toward personalized medicine
D Sahbani, B Strumbo, S Tedeschi, E Conte, GM Camerino, E Benetti, ...
Frontiers in Pharmacology 11, 327, 2020
Mandat: Government of Italy
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