Zobrazeno 1 - 10
of 618
pro vyhledávání: '"N. RIZZUTO"'
Autor:
L. Nobbio, D. Visigalli, D. Radice, E. Fiorina, A. Solari, G. Lauria, M. M. Reilly, A. Schenone, D. Pareyson, C. Marchesi, E. Salsano, L. Nanetti, C. Marelli, V. Scaioli, C. Ciano, M. Rimoldi, E. Rizzetto, F. Camozzi, E. Narciso, M. Grandis, M. Monti Bragadin, G. M. Fabrizi, T. Cavallaro, A. Casano, L. Bertolasi, I. Cabrini, K. Corra, N. Rizzuto, L. Santoro, M. Nolano, G. Vita, A. Mazzeo, M. Aguennouz, R. Di Leo, G. Majorana, N. Lanzano, F. Valenti, A. Quattrone, P. Valentino, R. Nistico, D. Pirritano, A. Lucisano, M. Canino, L. Padua, C. Pazzaglia, G. Granata, M. Foschini, F. Gemignani, F. Brindani, F. Vitetta, I. Allegri, F. Visioli, P. Bogani, NOLANO, MARIA, SANTORO, LUCIO, MANGANELLI, FIORE, PISCIOTTA, CHIARA
Publikováno v:
Brain
137 (2014): 1614–1620. doi:10.1093/brain/awu071
info:cnr-pdr/source/autori:Nobbio, Lucilla Alessandra; Visigalli, Davide; Radice, Davide; Fiorina, Elisabetta; Solari, Alessandra; Lauria, Giuseppe; Reilly, Mary M.; Santoro, Lucio; Schenone, Angelo E.; Pareyson, Davide, CMT-TRIAAL Group./titolo:PMP22 messenger RNA levels in skin biopsies: Testing the effectiveness of a Charcot-Marie-Tooth 1A biomarker/doi:10.1093%2Fbrain%2Fawu071/rivista:Brain (Print)/anno:2014/pagina_da:1614/pagina_a:1620/intervallo_pagine:1614–1620/volume:137
137 (2014): 1614–1620. doi:10.1093/brain/awu071
info:cnr-pdr/source/autori:Nobbio, Lucilla Alessandra; Visigalli, Davide; Radice, Davide; Fiorina, Elisabetta; Solari, Alessandra; Lauria, Giuseppe; Reilly, Mary M.; Santoro, Lucio; Schenone, Angelo E.; Pareyson, Davide, CMT-TRIAAL Group./titolo:PMP22 messenger RNA levels in skin biopsies: Testing the effectiveness of a Charcot-Marie-Tooth 1A biomarker/doi:10.1093%2Fbrain%2Fawu071/rivista:Brain (Print)/anno:2014/pagina_da:1614/pagina_a:1620/intervallo_pagine:1614–1620/volume:137
Charcot–Marie–Tooth disease type 1A (CMT1A) is associated with increased gene dosage for PMP22 . Therapeutic approaches are currently aiming at correcting PMP22 over-expression. It is unknown whether PMP22 can be used as a biological marker of di
Autor:
E. Frasson, L. Bertolasi, V. Bertasi, S. Fusina, L. Bartolomei, S. Vicentini, N. Rizzuto, A. Priori
Publikováno v:
Clinical Neurophysiology. 114:272-278
Objective : To investigate cortical excitability in patients with corticobasal degeneration (CBD) and to find a reliable diagnostic technique for differentiating CBD from Parkinson's disease (PD). Methods : Using a paired transcranial magnetic stimul
Autor:
B Bossi, G Ardolino, GM Fabrizi, L Bertolasi, T Cavallaro, S Polo, S Barbieri, N Rizzuto, A Priori
Publikováno v:
Journal of the Peripheral Nervous System. 8:29-58
Connexin 32 (Cx32), a protein involved in gap-junction formation, in the peripheral nervous system is mainly localized in non-compact myelin of paranodes and Schmidt-Lanterman incisures. Despite patients with Cx32 mutations have a polyneuropathic phe
Akademický článek
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Autor:
L. GALLO, U. FREO, M. D. BENEDETTI, G. MORETTO, C. RAVENNA, B. LUCCI, G. GIGLI, N. RIZZUTO, V. TOSO, G. L. RICCHIERI, S. BUTTIGNOL, L. BATTISTIN, G. PIZZOLATO, NACCARATO, MARCELLO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::74d2a92f5d5a9e6885923062b3d588e9
http://hdl.handle.net/11368/1689662
http://hdl.handle.net/11368/1689662
Autor:
C Antozzi, L Marzorati, F Cornelio, E. Bottacchi, M Sabatelli, M. Zarrelli, A. Bellini, C. Lunazzi, G. Lippi, N Rizzuto, A. Gomitoni, E. Fincati, P. Sorgato, F. Apollo, G. Guastella, A Bono, P. Tonali, Ettore Beghi, P. Simone, C. Lia, C. Castelli, E. Grasso, Graziella Bogliun, G. Bargagli, B Anghen, M Gresli, P. Crociani, P Santoro, M Mignogna, M Fasana, D. Zerbi, R. Affuso, L. Carenini, Pizza, L Amonisio, G. Ferrari, M Veratti, M. Marconi, M. Gentilini, Guido Cavaletti
Publikováno v:
Brain. 119:2053-2061
Publikováno v:
Clinical Neurology and Neurosurgery. 97:89-94
Sera from 3 patients with breast or ovarian tumors and paraneoplastic cerebellar degeneration (PCD) contained anti-Purkinje cell antibodies (PCAbs) which also bind to other neurons on frozen sections of adult rodent brain. PCAbs tested on new-born ro
Autor:
J. M. Dominguez-Roldan, F. Murillo-Cabezas, A. Munoz-Sanchez, A. Maestre, F. Porras, J. L. Santamaria-Mifsut, E. Facco, M. Munari, F. Baratto, A. U. Behr, R. Bruno, G. P. Giron, M. L. Sonnet, D. Perrot, D. Floret, C. Guillaume, B. Bui-Xuan, J. M. Vedrinne, J. Motin, G. Dall’Acqua, S. Cesaro, M. Giacomini, B. Allaouchiche, V. Moulaire, Y. Bouffard, N. Latronico, F. Fenzi, B. Guarneri, G. Tomelleri, P. Tonin, N. Rizzuto, A. Candiani, L. G. Lacguaniti, M. Irone, N. Zamperetti, A. Gulino, C. Pellegrin, M. Dan, C. Sandroni, A. Bareili, O. Piazza, F. Della Corte, A. Kovacs, M. Cucurachi, J. M. Sab, M. Sirodot, J. P. Straboni, D. Dorez, J. M. Dubols, Ph. Gaussorgues, D. Robert, B. Delafosse, N. Kopp, J. L. Faure, J. Neidecker, A. Parma, S. Marzorati, P. M. Rampini, M. Egidi, E. Calappi, R. Massci, M. Montolivo, M. Gemma, B. Regi, F. Fiacchino, J. Garnacho Montero, C. Ortiz Leyba, J. Madrazo Osuna, J. Jimenez Jimenez, R. Leal Noval, P. Chaparro Hernandez, A. Gervaix, M. Beghetti, M. Berner, A. Schneider, B. Rilliet, J. Berré, D. De Backer, J. J. Moraine, J. L. Vincent, R. J. Kahn, J. Latour, A. Reig, D. Ribera, M. C. Alemañ, J. L. Basco, M. López, M. Pastor, F. Carrasco, J. Zaplana, M. R. Ruiz, M. Sánchez, A. Boillot, G. Capellier, P. Balvay, A. Cordier, M. Tissot, F. Barale, M. Bricchi, S. Franceschetti
Publikováno v:
Intensive Care Medicine. 18:S203-S208
Publikováno v:
Clinical neuropathology. 19(4)
To detect mitochondrial lesions in the spinal cord from an autoptic case of myoclonus epilepsy with ragged-red fibers (MERRF) that harbored the A8344G mutation and was deemed to be free of pathological abnormalities in the spinal cord after conventio
G.P.3.11 Increased protein nitration in mitochondrial diseases: Evidence for vessel wall involvement
Autor:
G. Vattemi, Y. Mechref, M. Marini, P. Tonin, P. Minuz, L. Grigoli, null Klouckova, C. Chiamulera, A. Meneguzzi, M. Di Chio, V. Tedesco, L. Lovato, M. Degan, M. Filosto, G. Arcaro, M. Riccadonna, V. Guglielmi, G. Fumagalli, N. Rizzuto, A. Lechi, M. Novotny, G. Tomelleri
Publikováno v:
Neuromuscular Disorders. 19:564-565