CASARI, GIORGIO NEVIO

CASARI, GIORGIO NEVIO  

Facoltà di Medicina e Chirurgia  

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2 POINT MUTATIONS WITHIN THE ADDUCIN GENES ARE INVOLVED IN BLOOD-PRESSURE VARIATION 1-gen-1994 Bianchi, G; Tripodi, G; Casari, GIORGIO NEVIO; Salardi, S; Barber, Br; Garcia, R; Leoni, P; Torielli, L; Cusi, D; Ferrandi, M; Pinna, La; Baralle, Fe; Ferrari, P.
A GENOMIC APPROACH TO IDENTIFY NEW GENES RESPONSIBLE FOR INHERITED MOTOR AND CMT2 NEUROPATHIES: A COLLABORATIVE STUDY 1-gen-2016 Previtali, Sc; Fabrizi, Gm; Manganelli, F; Mazzeo, A; Pareyson, D; Schenone, A; Taroni, F; Vita, G; Bellone, E; Ferrarini, M; Magri, S; Scarlato, M; Riva, N; Lunetta, C; Carrera, P; Bucci, G; Mandich, P; Penco, S; Lazarevic, D; Cittaro, D; Jordanova, A; Reilly, Mm; Casari, GIORGIO NEVIO; Ferrari, M; Comi, Giancarlo; Bolino, A.
A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection 1-gen-2020 Casanova, J. -L.; Su, H. C.; Abel, L.; Aiuti, A.; Almuhsen, S.; Arias, A. A.; Bastard, P.; Biggs, C.; Bogunovic, D.; Boisson, B.; Boisson-Dupuis, S.; Bolze, A.; Bondarenko, A.; Bousfiha, A.; Brodin, P.; Bustamante, J.; Butte, M.; Casari, G.; Ciancanelli, M.; Cobat, A.; Condino-Neto, A.; Cooper, M.; Dalgard, C.; Espinosa, S.; Feldman, H.; Fellay, J.; Franco, J. L.; Hagin, D.; Itan, Y.; Jouanguy, E.; Lucas, C.; Mansouri, D.; Meyts, I.; Milner, J.; Mogensen, T.; Morio, T.; Ng, L.; Notarangelo, L. D.; Okada, S.; Ozcelik, T.; Palacin, P. S.; Planas, A.; Prando, C.; Puel, A.; Pujol, A.; Redin, C.; Renia, L.; Rodriguez Gallego, J. C.; Quintana-Murci, L.; Sancho-Shimizu, V.; Sankaran, V.; Seppanen, M. R. J.; Shahrooei, M.; Snow, A.; Spaan, A.; Tangye, S.; Tur, J. P.; Turvey, S.; Vinh, D. C.; von Bernuth, H.; Wang, X.; Zawadzki, P.; Zhang, Q.; Zhang, S.
A large family with idiopathic basal ganglia calcifications not linked to chromosome 14q 1-gen-2005 Volpato, Cb; Buffone, E; De Grandi, A; Tezzon, F; Casari, GIORGIO NEVIO; Pramstaller, Pp
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3 1-gen-2002 Muglia, M; Magariello, A; Nicoletti, G; Patitucci, A; Gabriele, Al; Conforti, Fl; Mazzei, R; Caracciolo, M; Casari, GIORGIO NEVIO; Ardito, B; Lastilla, M; Gambardella, A; Quattrone, A.
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 1-gen-2001 Muglia, M; Magariello, A; Nicoletti, G; Patitucci, A; Gabriele, Al; Conforti, Fl; Mazzei, R; Casari, GIORGIO NEVIO; Ardito, B; Lastilla, M; Mangone, L; Gambardella, A; Quattrone, A.
A large southern Italian family with autosomal dominant dementia and extrapyramidal features not linked to chromosome 17 1-gen-1999 Filla, A; Bruni, A; Terme, L; De Michele, G; Volpe, G; Coppola, G; Salvatore, E; Calabrese, O; Castaldo, I; Casari, GIORGIO NEVIO; Ballabio, A; Caruso, G; Cocozza, S.
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2 1-gen-2004 Striano, P; Chifari, R; Striano, S; de Fusco, M; Elia, M; Guerrini, R; Casari, GIORGIO NEVIO; Canevini, Mp
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 1-gen-2000 Gambardella, A; Annesi, G; De Fusco, M; Patrignani, A; Aguglia, U; Annesi, F; Pasqua, Aa; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Casari, GIORGIO NEVIO; Quattrone, A.
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3 1-gen-1998 De Michele, G; De Fusco, M; Cavalcanti, F; Filla, A; Marconi, R; Volpe, G; Monticelli, A; Ballabio, A; Casari, GIORGIO NEVIO; Cocozza, S.
A NOVEL BIPARTITE SPLICING ENHANCER MODULATES THE DIFFERENTIAL PROCESSING OF THE HUMAN FIBRONECTIN EDA EXON 1-gen-1994 Caputi, M; Casari, GIORGIO NEVIO; Guenzi, S; Tagliabue, R; Sidoli, A; Melo, Ca; Baralle, Fe
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood 1-gen-2004 Bassi, Mt; Bresolin, N; Tonelli, A; Nazos, K; Crippa, F; Baschirotto, C; Zucca, C; Bersano, A; Dolcetta, D; Boneschi, Fm; Barone, V; Casari, GIORGIO NEVIO
A novel truncated form of eNOS associates with altered vascular function 1-gen-2014 Galluccio, E; Cassina, L; Russo, I; Gelmini, F; Setola, E; Rampoldi, L; Citterio, L; Rossodivita, A; Kamami, M; Colombo, A; Alfieri, Ottavio; Carini, M; Bosi, Emanuele; Trovati, M; Piatti, P; Monti, Ld; Casari, GIORGIO NEVIO
A recessive variant of the Romano-Ward Long-QT syndrome? 1-gen-1998 Priori, Sg; Schwartz, Pj; Napolitano, C; Bianchi, L; Dennis, A; De Fusco, M; Brown, Am; Casari, GIORGIO NEVIO
A reduced activity of the Na-K ATPase is responsible for familial hemiplegic migraine 1-gen-2003 Casari, G; De Fusco, M; Aridon, P; Silvestri, L; Atorino, L; Rampoldi, L; Ballabio, A; Marconi, R
A thiazide test for the diagnosis of renal tubular hypokalemic disorders 1-gen-2007 Colussi, G; Bettinelli, A; Tedeschi, S; De Ferrari, Me; Syren, Ml; Borsa, N; Mattiello, C; Casari, GIORGIO NEVIO; Bianchetti, Mg
A TRAPPC6B splicing variant associates to restless legs syndrome 1-gen-2016 Aridon, Paolo; De Fusco, Maurizio; Winkelmann, Juliane W.; Zucconi, Marco; Arnao, Valentina; FERINI STRAMBI, Luigi; Casari, GIORGIO NEVIO
Aldosterone influences serum magnesium in Gitelman syndrome 1-gen-2000 Bettinelli, A; Consonni, D; Bianchetti, Mg; Colussi, G; Casari, GIORGIO NEVIO
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics 1-gen-2003 Rampoldi, L; Caridi, G; Santon, D; Boaretto, F; Bernascone, I; Lamorte, G; Tardanico, R; Dagnino, M; Colussi, G; Scolari, F; Ghiggeri, Gm; Amoroso, A; Casari, GIORGIO NEVIO
Allelism of medullary cystic disease, familial juvenile hyperuricemic nephropathy and glomerulocystic kidney disease caused by delayed uromodulin trafficking to plasma membrane and endoplasmic reticulum retention 1-gen-2006 Rampoldi, L; Lamorte, G; Bernascone, I; Caridi, G; Santon, D; Boaretto, F; Tardanico, R; Dagnino, M; Colussi, G; Scolari, F; Ghiggeri, Gm; Amoroso, A; Casari, GIORGIO NEVIO; Mazza, Davide