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Results: 1-10 |
Results: 10
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy
Authors: Zanusso, G Vattemi, G Ferrari, S Tabaton, M Pecini, E Cavallaro, T Tomelleri, G Filosto, M Tonin, P Nardelli, E Rizzuto, N Monaco, S
Citation: G. Zanusso et al., Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy, BRAIN PATH, 11(2), 2001, pp. 182-189
A somatic and germline mosaic mutation in MPZ/P-0 mimics recessive inheritance of CMT1B
Authors: Fabrizi, GM Ferrarini, M Cavallaro, T Jarre, L Polo, A Rizzuto, N
Citation: Gm. Fabrizi et al., A somatic and germline mosaic mutation in MPZ/P-0 mimics recessive inheritance of CMT1B, NEUROLOGY, 57(1), 2001, pp. 101-105
PMP22 related congenital hypomyelination neuropathy
Authors: Fabrizi, GM Simonati, A Taioli, F Cavallaro, T Ferrarini, M Rigatelli, F Pini, A Mostacciuolo, ML Rizzuto, N
Citation: Gm. Fabrizi et al., PMP22 related congenital hypomyelination neuropathy, J NE NE PSY, 70(1), 2001, pp. 123-126
Immunohistochemical demonstration of spinal ventral horn cells involvementin a case of "myoclonus epilepsy with ragged red fibers" (MERRF)
Authors: Sparaco, M Cavallaro, T Rossi, G Rizzuto, N
Citation: M. Sparaco et al., Immunohistochemical demonstration of spinal ventral horn cells involvementin a case of "myoclonus epilepsy with ragged red fibers" (MERRF), CLIN NEUR, 19(4), 2000, pp. 200-207
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: Electrophysiological abnormalities and sural nerve biopsy
Authors: Polo, A Aldegheri, R Bongiovanni, LG Cavallaro, T Rizzuto, N
Citation: A. Polo et al., Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: Electrophysiological abnormalities and sural nerve biopsy, NEUROPEDIAT, 31(3), 2000, pp. 148-150
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero
Authors: Fabrizi, GM Taioli, F Cavallaro, T Rigatelli, F Simonati, A Mariani, G Perrone, P Rizzuto, N
Citation: Gm. Fabrizi et al., Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero, ACT NEUROP, 100(3), 2000, pp. 299-304
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22
Authors: Simonati, A Fabrizi, GM Pasquinelli, A Taioli, F Cavallaro, T Morbin, M Marcon, G Papini, M Rizzuto, N
Citation: A. Simonati et al., Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22, NEUROMUSC D, 9(4), 1999, pp. 257-261
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a pointmutation of peripheral myelin protein-22
Authors: Fabrizi, GM Cavallaro, T Taioli, F Orrico, D Morbin, M Simonati, A Rizzuto, N
Citation: Gm. Fabrizi et al., Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a pointmutation of peripheral myelin protein-22, NEUROLOGY, 53(4), 1999, pp. 846-851
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family
Authors: Casali, C Fabrizi, GM Santorelli, FM Colazza, G Villanova, M Dotti, MT Cavallaro, T Cardaioli, E Battisti, C Manneschi, L DiGennaro, GC Fortini, D Spadaro, M Morocutti, C Federico, A
Citation: C. Casali et al., Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family, NEUROLOGY, 52(5), 1999, pp. 1103-1104
Novel mutation of the P-0 extracellular domain causes a Dejerine-Sottas syndrome
Authors: Fabrizi, GM Cavallaro, T Morbin, M Simonati, A Taioli, F Rizzuto, N
Citation: Gm. Fabrizi et al., Novel mutation of the P-0 extracellular domain causes a Dejerine-Sottas syndrome, J NE NE PSY, 66(3), 1999, pp. 386-389
Risultati: 1-10 |