SCHENONE, ANGELO

SCHENONE, ANGELO  

100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili  

Mostra records
Risultati 1 - 20 di 326 (tempo di esecuzione: 0.019 secondi).
Titolo Data di pubblicazione Autore(i) File
"Limbic encephalitis with acute onset and Hu antibodies treated with rituximab: Paraneoplastic or non-paraneoplastic disorder?" 1-gen-2019 Lapucci, C; Benedetti, L; Tavarelli, C; Serrati, C; Godani, Martina; Schenone, A; Franciotta, D
"Pure" meningeal carcinomatosis as the autopsy-proven sole manifestation of an undetected cancer 1-gen-1992 Leonardi, A; Dagnino, N; Farinelli, M; Gambini, C; Ribizzi, G; Schenone, A; Mancardi, G L
147th ENMC International Workshop: Guideline on processing and evaluation of sural nerve biopsies, 15-17 December 2006, Naarden, The Netherlands. 1-gen-2008 Sommer, C; Brandner, S; Dyck, Pj; Magy, L; Mellgren, Si; Morbin, M; Schenone, Angelo; Tan, E; Weis, J.
17p11.2 duplication is a common finding in sporadic cases of charcot-marie-tooth type 1 1-gen-1994 Mancardi, G. L.; Uccelli, A.; Bellone, E.; Sghirlanzoni, A.; Mandich, P.; Pareyson, D.; Schenone, A.; Abbruzzese, M.; Ajmar, F.
[Hereditary sensory motor neuropathy: degenerative disease or a disease with an immune-mediated pathogenesis?]. 1-gen-1989 Cadoni, Angela; Zicca, Antonio; Mancardi, GIOVANNI LUIGI; DE MARTINI, Isabella; Schenone, Angelo; Zaccheo, D.
[Schwann cells in acute and chronic Guillain-Barré syndrome]. 1-gen-1987 Cadoni, Angela; Zicca, Antonio; Schenone, Angelo; DE MARTINI, Isabella; Mancardi, GIOVANNI LUIGI
A CASE OF BIALLELIC SORD MUTATIONS ASSOCIATED WITH DISTAL WEAKNESS AND HISTOLOGICAL SIGNS OF MYOPATHY 1-gen-2023 Massucco, S; Fiorillo, C; Gemelli, C; Bellone, E; Patrone, S; Mandich, P; Scarsi, E; Faedo, E; Marinelli, L; Mongini, T; Traverso, M; Schenone, A; Grandis, M
A case of secondary syphilis presenting as optic neuritis 1-gen-2010 Bandettini di Poggio, M; Primavera, Alberto; Capello, E; Bandini, F; Mazzarello, G; Viscoli, Claudio; Schenone, Angelo
A case series of parainfectious Guillain-Barré syndrome linked to influenza A (H1N1) virus infection 1-gen-2021 Grisanti, S. G.; Franciotta, D.; Garnero, M.; Zuppa, A.; Massa, F.; Mobilia, E. M.; Pesce, G.; Schenone, A.; Benedetti, L.
A cross-sectional study investigating frequency and features of definitely diagnosed diabetic painful polyneuropathy 1-gen-2018 Truini, Andrea; Spallone, Vincenza; Morganti, Roberto; Tamburin, Stefano; Zanette, Giampietro; Schenone, Angelo; De Michelis, Chiara; Tugnoli, Valeria; Simioni, Valentina; Manganelli, Fiore; Dubbioso, Raffaele; Lauria, Giuseppe; Lombardi, Raffaella; Jann, Stefano; De Toni Franceschini, Luisa; Tesfaye, Solomon; Fiorelli, Marco; Spagnoli, Alessandra; Cruccu, Giorgio
A misleading presentation of Mohr–Tranebjaerg syndrome: what is hidden behind an axonal neuropathy? 1-gen-2022 Geroldi, Alessandro; Trevisan, Lucia; Gaudio, Andrea; Gotta, Fabio; Patrone, Serena; Origone, Paola; Grandis, Marina; Gemelli, Chiara; Schenone, Angelo; Accogli, Andrea; Zara, Federico; Mandich, Paola; Bellone, Emilia
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs) 1-gen-2019 Pareyson, D.; Stojkovic, T.; Reilly, M. M.; Leonard-Louis, S.; Laura, M.; Blake, J.; Parman, Y.; Battaloglu, E.; Tazir, M.; Bellatache, M.; Bonello-Palot, N.; Levy, N.; Sacconi, S.; Guimaraes-Costa, R.; Attarian, S.; Latour, P.; Sole, G.; Megarbane, A.; Horvath, R.; Ricci, G.; Choi, B. -O.; Schenone, A.; Gemelli, C.; Geroldi, A.; Sabatelli, M.; Luigetti, M.; Santoro, L.; Manganelli, F.; Quattrone, A.; Valentino, P.; Murakami, T.; Scherer, S. S.; Dankwa, L.; Shy, M. E.; Bacon, C. J.; Herrmann, D. N.; Zambon, A.; Tramacere, I.; Pisciotta, C.; Magri, S.; Previtali, S. C.; Bolino, A.
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol 1-gen-2006 Pareyson, D; Schenone, A; Fabrizi, Gm; Santoro, L; Padua, L; Quattrone, A; Vita, G; Gemignani, F; Visioli, F; Solari, A; Salsano, E; Scaioli, V; Ciano, C; Rimoldi, M; Lauria, G; Rizzetto, E; Camozzi, F; Grandis, M; Narciso, E; Nobbio, L; Benedetti, L; Rizzuto, N; Cavallaro, T; Bertolasi, L; Casano, A; Manganelli, F; Nolano, M; Pazzaglia, C; Valentino, P; Nisticò, R; Pirritano, D; Lucisano, A; Canino, M; Mazzeo, A; Aguennouz, M; Di Leo, R; Girlanda, P; Majorana, G; Ciranni, A; Lanzano, N; Brindani, F; Lettieri, C; Bogani, P; Hughes, Rac; Mancardi, Gl; Cavaletti, G; Galimberti, S; Radice, D; Calabrese, D; Ferrari, G.
A nationwide retrospective analysis on the effect of immune therapies in patients with chronic inflammatory demyelinating polyradiculoneuropathy 1-gen-2010 D., Cocito; I., Paolasso; G., Antonini; L., Benedetti; C., Briani; C., Comi; R., Fazio; S., Jann; S., Matà; A., Mazzeo; M., Sabatelli; E., Nobile Orazio; Schenone, Angelo
A novel compound heterozygous mutation ofC20orf54gene associated with Brown-Vialetto-Van Laere syndrome in an Italian family 1-gen-2013 BANDETTINI DI POGGIO, MONICA LAURA; S., Gagliardi; Pardini, Matteo; E., Marchioni; M., Monti Bragadin; L., Reni; L., Doria Lamba; Roccatagliata, Luca; M., Ceroni; Schenone, Angelo; C., Cereda
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers 1-gen-2023 Geroldi, A.; Tozza, S.; Fiorillo, C.; Nolano, M.; Fossa, P.; Vitale, F.; Domi, R.; Gaudio, A.; Mammi, A.; Patrone, S.; Barbera, A. L.; Origone, P.; Ponti, C.; Sanguineri, F.; Zara, F.; Cataldi, M.; Salpietro, V.; Venturi, C. B.; Massucco, S.; Schenone, A.; Manganelli, F.; Mandich, P.; Bellone, E.; Gotta, F.
A novel mutation in the N-terminal acting-binding domain of Filamin C protein causing a distal myofibrillar myopathy 1-gen-2019 Gemelli, Chiara; Prada, Valeria; Fiorillo, Chiara; Fabbri, Sabrina; Maggi, Lorenzo; Geroldi, Alessandro; Gibertini, Sara; Mandich, Paola; Trevisan, Lucia; Fossa, Paola; Tagliafico, Alberto Stefano; Schenone, Angelo; Grandis, Marina.
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect 1-gen-2004 DI MARIA, Emilio; Gulli, R.; Balestra, P.; Cassandrini, D.; Pigullo, S.; DORIA LAMBA, L.; Bado, M.; Schenone, Angelo; Ajmar, Franco; Mandich, Paola; Bellone, Emilia
A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea 1-gen-2018 Bommarito, G.; Cellerino, M.; Prada, V.; Venturi, C.; Capellari, S.; Cortelli, P.; Mancardi, G. L.; Parchi, P.; Schenone, A.
A P2X7 antagonist improves muscle strength and motor distal amplitude in CMT1A rats: preliminary results from an in vivo trial 1-gen-2014 Sociali, Giovanna; Prukop, Thomas; Cervellini, Ilaria; Nobbio, Lucilla; Bruzzone, Santina; Flora, Antonio De; Schenone, Angelo; Sereda2, Michael W. .