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Titolo Data di pubblicazione Autore(i) File
Guillain barré syndrome of axonal type in a multple sclerosis patient: Fortuitous association or linked disorders? 1-gen-1997 Roccatagliata, L.; Capello, E.; Schenone, A.; Inglese, M.; Nobbio, L.; Grandis, M.; Maritato, F.; Abbruzzese, M.; Mancardi, G. L.
Prevalence of right-to-left shunt on transcranial doppler in an Italian family with CADASIL 1-gen-2000 Angeli, S; DEL SETTE, M; Assini, A; Grandis, Marina; Caprera, P; Gandolfo, Carlo
PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A. 1-gen-2001 Nobbio, Lucilla; Mancardi, GIOVANNI LUIGI; Grandis, Marina; G., Levi; U., Suter; K. A., Nave; A. J., Windebank; Abbruzzese, Michele; Schenone, Angelo
Insulin treatment enhances expression of IGF-I in sural nerves of diabetic patients. 1-gen-2001 Grandis, Marina; Nobbio, Lucilla; Abbruzzese, Michele; L., Banchi; Minuto, Francesco; A., Barreca; S., Garrone; Mancardi, GIOVANNI LUIGI; Schenone, Angelo
Very high prevalence of right-to-left shunt on transcranial doppler in an Italian family with cerebral atosomal dominant angiopathy with subcortical infarction and leukoencephalopathy 1-gen-2001 Angeli, S; Carrera, P; DEL SETTE, M; Assini, A; Grandis, Marina; Biancolin, D; Ferari, M; Gandolfo, Carlo
Different movement disorders responsive to carbamazepine in patients with brainstem focal lesions 1-gen-2001 L., Benedetti; C., Finocchi; Grandis, Marina; A., Murialdo; Marinelli, Lucio; Abbruzzese, Michele; Marchese, Roberta; Schenone, Angelo; Abbruzzese, Giovanni
Early electophysiological changes in transgenic rat model of charcot-marie-tooth. 1-gen-2001 Grandis, Marina; Abbruzzese, Michele; Lunardi, Gianluigi; Nobbio, L.; Mancardi, GIOVANNI LUIGI; Leandri, Massimo; Schenone, Angelo
The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter. 1-gen-2001 M., Musso; P., Balestra; Bellone, Emilia; D., Cassandrini; E. D., Maria; L. L., Doria; Grandis, Marina; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; G., Levi; F., Ajmar; Mandich, Paola
Neuropatie diabetiche 1-gen-2002 Schenone, Angelo; Benedetti, L.; Grandis, Marina
Phenotipic clustering in MPZ mutations. 1-gen-2004 Shy, M. E.; Jani, A; Krajewski, K; Grandis, Marina; Lewis, R. A.; Li, J; Shy, R. R.; Balsamo, J; Lilien, J; Garbern, J. Y.; Kamholz, J.
Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease. 1-gen-2004 Grandis, Marina; Leandri, Massimo; Vigo, Tiziana; Cilli, M; Sereda, Mw; Gherardi, G; Benedetti, L; Mancardi, GIOVANNI LUIGI; Abbruzzese, Michele; Nave, Ka; Nobbio, Lucilla; Schenone, Angelo
Mycophenolate mofetil in dysimmune neuropathies: a preliminary study. 1-gen-2004 Benedetti, L; Grandis, Marina; Nobbio, Lucilla; Beronio, A; Ghiglione, E; Manzino, M; Primavera, Alberto; Mancardi, GIOVANNI LUIGI; Schenone, Angelo
Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A disease. 1-gen-2004 Nobbio, Lucilla; Vigo, T; Abbruzzese, Michele; Levi, G; Brancolini, C; Mantero, S; Grandis, Marina; Benedetti, L; Mancardi, GIOVANNI LUIGI; Schenone, Angelo
Genotype-Phenotype correlations of MPZ mutations 1-gen-2005 Cadoni, Angela; La Padula, V.; Vigo, Tiziana; Jain, M; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; Grandis, Marina; Kamholz, J.; Shy, M. E.
Immunoelectron microscopy study of skin biopsies from patients with different types of Charcot-Marie-tooth neuropathy 1-gen-2005 Schenone, Angelo; Cozzani, EMANUELE CLAUDIO; Ghandour, K; Pu, Q; Grandis, M; Cadoni, Angela; La Padula, V; Hatfield, J; Shy, Me; Li, J.
Current Therapy for Charcot-Marie-Tooth Disease. 1-gen-2005 Grandis, Marina; Shy, Me
Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside 1-gen-2005 Li, J; Bai, Y; Ghandour, K; Qin, P; Grandis, Marina; Trostinskaia, A; Ianakova, E; Wu, X; Schenone, Angelo; Vallat, Jm; Kupsky, Wj; Hatfield, J; Shy, M. E.
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.
Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration. 1-gen-2006 Li, J; Bai, Y; Ianakova, E; Grandis, Marina; Uchwat, F; Trostinskaia, A; Krajewski, Km; Garbern, J; Kupsky, Wj; COMP NEUROL, SHY M. E. J.
Cellular and molecular differences between early and late onset myelin protein zero mutations 1-gen-2007 Grandis, Marina; Vigo, Tiziana; Jain, M.; La Padula, V.; Scazzola, S.; Passalacqua, Mario; Benvenuto, F.; Kamholz, J.; Shy, M. E.; Schenone, Angelo
Mostrati risultati da 1 a 20 di 133
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