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Sfoglia per Rivista  NEPHROLOGY DIALYSIS TRANSPLANTATION

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Erythrocyte calcium influx is related to severity of ventricular arrhytmias in uremic patients 1-gen-2001 Soldati, L; Adamo, D; Manunta, Paolo; Stella, P; Ciurlino, D; Spotti, D; Slaviero, G; Melandri, M; Cusi, D; Bianchi, G; Vezzoli, G.
EUNEFRON, the European Network for the Study of Orphan Nephropathies 1-gen-2009 Devuyst, O; Meij, I; Jeunemaitre, X; Ronco, P; Antignac, C; Christensen, Ei; Knoers, Nv; Levtchenko, En; Deen, Pm; Muller, D; Wagner, Ca; Rampoldi, L; van't Hoff, Wg
Functional consequences of a novel uromodulin mutation in a family with familial juvenile hyperuricaemic nephropathy 1-gen-2004 Tinschert, S; Ruf, N; Bernascone, I; Sacherer, K; Lamorte, G; Neumayer, Hh; Nurnberg, P; Luft, Fc; Rampoldi, L
Interleukin-27 is a potential marker for the onset of post-transplant malignancies 1-gen-2018 Pontrelli, Paola; Rascio, Federica; Zaza, Gianluigi; Accetturo, Matteo; Simone, Simona; Infante, Barbara; Furian, Lucrezia; Castellano, Giuseppe; Ditonno, Pasquale; Battaglia, Michele; Cormio, Luigi; Carrieri, Giuseppe; Lupo, Antonio; Rigotti, Paolo; Gesualdo, Loreto; Stallone, Giovanni; Grandaliano, Giuseppe
Metabolic results 3 years after simultaneous pancreas-kidney transplantation 1-gen-2005 Secchi, Antonio; Malaisse, J; Caldara, R.
MPO antibody-positive vasculitis in a patient with psoriatic arthritis and gold-induced membranous glomerulonephritis 1-gen-1998 Quarenghi, Mi; DEL VECCHIO, L; Casartelli, D; Manunta, Paolo; Rossi, R.
The mutation c.1196_1202dup7bp (p.Ser402X) in the SLC12A3 gene clusters in Italian Gitelman syndrome patients and reflects the presence of a common ancestor 1-gen-2011 Syren, Ml; Ghiringhelli, Nb; Bettinelli, A; Colussi, G; Vargas-Poussou, ; Tammaro, F; Coviello, Da; Tedeshi, S; Calò, L; Ciuoli, C; Deferrari, E; Materassi, M; Orrico, A; Vezzoli, G
The need for a multi-disciplinary reflection about frailty and cognitive impairment in chronic kidney disease 1-gen-2023 Farisco, M.; Zecchino, I.; Capasso, G.; Andrade, A.; Bachmann, M.; Bumblyte, I.; Covic, A. C.; Delgado, P.; Endlich, N.; Engvig, A.; Fouque, D.; Franssen, C.; Frische, S.; Garneata, L.; Gesualdo, L.; Giannakou, K.; Goumenos, D.; Kartal, A. T.; Mani, L. Y.; Marti, H. P.; Mayer, C.; Nielsen, R.; Pešić, V.; Rroji, M.; Sakkas, G.; Spasovski, G.; Stevens, K. I.; Vazelov, E.; Viggiano, D.; Zacharia, L.; Ferreira, A. C.; Malyszko, J.; Hoorn, E.; Figurek, A.; Unwin, R.; Wagner, C.; Wanner, C.; Bruchfeld, A.; Pepin, M.; Wieçek, A.; Nitsch, D.; Fridolin, I.; Hafez, G.; Soler, M. J.; Barbieri, M.; Batinić, B.; Carrasco, L.; Carriazo, S.; Gansevoort, R.; Martino, Gianvito; Raso, F. M.; Nistor, I.; Ortiz, A.; Paolisso, G.; Rastenytė, D.; Stefan, G.; Tedeschi, G.; Massy, Z. A.; Bikbov, B.; Endlich, K. H.; Godefroy, O.; Chillon, J. M.; Kossioni, A.; Kurganaite, J.; Perico, N.; Remuzzi, G.; Grodzicki, T.; Trepiccione, F.; Zoccali, C.; Arici, M.; Blankestijn, P.; Eckardt, K. U.; Fliser, D.; Jiménez, E. G.; König, M.; Rychlik, I.; Deleidi, M.; Reusz, G.
Neuropeptide Y as a risk factor for cardiorenal disease and cognitive dysfunction in chronic kidney disease: translational opportunities and challenges 1-gen-2022 Zoccali, C.; Ortiz, A.; Blumbyte, I. A.; Rudolf, S.; Beck-Sickinger, A. G.; Malyszko, J.; Spasovski, G.; Carriazo, S.; Viggiano, D.; Kurganaite, J.; Sarkeviciene, V.; Rastenyte, D.; Figurek, A.; Rroji, M.; Mayer, C.; Arici, M.; Martino, G.; Tedeschi, G.; Bruchfeld, A.; Spoto, B.; Rychlik, I.; Wiecek, A.; Okusa, M.; Remuzzi, G.; Mallamaci, F.
A new clinical multivariable model that predicts postoperative acute kidney injury: impact of endogenous ouabain 1-gen-2014 Simonini, M; Lanzani, C; Bignami, E; Casamassima, N; Frati, E; Meroni, R; Messaggio, E; Alfieri, Ottavio; Hamlyn, J; Body, Sc; Collard, Cd; Zangrillo, Alberto; Manunta, Paolo
Phenotypic and genetic heterogeneity in Dent's disease–the results of an Italian collaborative study 1-gen-2006 Tosetto, E; Ghiggeri, Gm; Emma, F; Barbano, G; Carrea, A; Vezzoli, G; Torregrossa, R; Cara, M; Ripanti, G; Ammenti, A; Peruzzi, L; Murer, L; Ratsch, Im; Citron, L; Gambaro, G; D'Angelo, A; Anglani, F
Potential role of effector memory T cells in chronic T cell-mediated kidney graft rejection 1-gen-2016 Curci, Claudia; Sallustio, Fabio; Serino, Grazia; De Palma, Giuseppe; Trpevski, Mirko; Fiorentino, Marco; Rossini, Michele; Quaglia, Marco; Valente, Marialuisa; Furian, Lucrezia; Toscano, Alessia; Mazzucco, Gianna; Barreca, Antonella; Bussolino, Stefania; Gesualdo, Loreto; Stratta, Piero; Rigotti, Paolo; Citterio, Franco; Biancone, Luigi; Schena, Francesco P.
Protein trafficking defects in inherited kidney diseases 1-gen-2014 Schaeffer, C; Creatore, A; Rampoldi, L
The risk of nephrolithiasis is causally related to inactive matrix Gla protein, a marker of vitamin K status: a Mendelian randomization study in a Flemish population 1-gen-2017 Wei, Fang Fei; Thijs, Lutgarde; Zhang, Zhen Yu; Jacobs, Lotte; Yang, Wen Yi; Salvi, Erika; Citterio, Lorena; Cauwenberghs, Nicholas; Kuznetsova, Tatiana; E. A. Drummen, Nadja; Hara, Azusa; Manunta, Paolo; Li, Yan; Verhamme, Peter; Allegaert, Karel; Cusi, Daniele; Vermeer, Cees; Staessen, Jan A.
The young girl with renovascular hypertension of unknown origin 1-gen-1997 Manunta, Paolo; Lanzani, C; Chiesa, R; Castellano, R; Ianello, A; Melissano, Germano; Venturini, M; DEL MASCHIO, Alessandro; Cusi, D.
The young girl with renovascular hypertension of unknown origin 1-gen-1997 Manunta, Paolo; Lanzani, C; Chiesa, Roberto; Castellano, F; Ianello, A; Melissano, Germano; Venturini, M; DEL MASCHIO, Alessandro; Cusi, D.
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