RIZZUTO, Nicolo'

RIZZUTO, Nicolo'  

DIPARTIMENTO DI SCIENZE NEUROLOGICHE E DELLA VISIONE  

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Risultati 1 - 20 di 263 (tempo di esecuzione: 0.017 secondi).
Titolo Data di pubblicazione Autore(i) File
[4 cases of Jakob-Creutzfeldt's disease] 1-gen-1976 E., Nardelli; Rizzuto, Nicolo'
A 49-year-old man with neuropsychiatric symptoms followed by progressive cognitive decline. 1-gen-2006 Zanusso, Gianluigi; Ferrari, Sergio; Conte, S; Mellina, V; Sacchi, V; Rizzuto, Nicolo'; Monaco, Salvatore
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 1-gen-1995 Gomez, Maria Macarena; C., Perusi; N., Brutti; M. A., Farnetani; M. A., Margollicci; Rizzuto, Nicolo'; Pignatti, Pierfranco; Salviati, Alessandro
A case of multifocal CIS with unusual MRI features suggestive of Balo's concentric sclerosis 1-gen-2006 F., Rossi; P., Invernizzi; S., Rasia; E., Turri; Turatti, Marco; Gajofatto, Alberto; Bonetti, Bruno; Rizzuto, Nicolo'; M. D., Benedetti
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 1-gen-2000 Simonati, Alessandro; Santorum, E.; Tessa, A.; Polo, A.; Simonetti, F.; DALLA BERNARDINA, Bernardo; Santorelli, F. M.; Rizzuto, Nicolo'
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 1-gen-1995 Gomez, Maria Macarena; Sangalli, Antonella; Mottes, Monica; Perusi, C; Pignatti, Pierfranco; Rizzuto, Nicolo'; Salviati, Alessandro
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 1-gen-2001 Gomez-Lira, M.; Mottes, M.; Perusi, C.; Pignatti, P. F.; Rizzuto, N.; Gatti, R.; Salviati, A.
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 1-gen-2007 Ferrarini, Moreno; Squintani, G.; Cavallaro, Tiziana; Ferrari, Sergio; Rizzuto, Nicolo'; Fabrizi, Gian Maria
Activation of NF-kappaB and c-jun transcription factors in multiple sclerosis lesions. Implications for oligodendrocyte pathology 1-gen-1999 Bonetti, Bruno; Stegagno, C.; Cannella, B.; Rizzuto, Nicolo'; Moretto, G.; Raine, C. S.
Acute reversible paralysis in critically ill patients 1-gen-1993 Latronico, N.; Fenzi, Flavio; Boniotti, C.; Guarneri, B.; Tonin, Paola; Tomelleri, Giuliano; De Maria, G.; Antonini, L.; Rizzuto, Nicolo'; Candiani, A.
Adhesion molecules expression on the vascular endothelium of peripheral nerve in HIV-associated Distal Sensory Polyneuropathy 1-gen-2005 Fenzi, Flavio; Rossi, F.; Cavallaro, T.; Ferrari, S.; Rizzuto, Nicolo'
[Alzheimer's disease. Histopathological and ultrastructural study of 6 cases (author's transl)] 1-gen-1976 A., Iannucci; E., Nardelli; Rizzuto, Nicolo'
Amyotrophy in Shy-Drager syndrome. 1-gen-1983 P., Montagna; P., Martinelli; Rizzuto, Nicolo'; Salviati, Alessandro; F., Rasi; E., Lugaresi
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 1-gen-1978 Perbellini, Luigi; D., De Grandis; F., Semenzato; Rizzuto, Nicolo'; Simonati, Alessandro
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 1-gen-2004 Frigerio, R.; Fabrizi, Gian Maria; Ferrarini, Moreno; Cavallaro, Tiziana; Brighina, L.; Santoro, P.; Agostoni, E.; Cavaletti, G.; Rizzuto, Nicolo'; Ferrarese, C.
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 1-gen-1988 Fenzi, Flavio; Bongiovanni, Luigi Giuseppe; Fincati, E.; Pampanin, M.; Tomelleri, Giuliano; Rizzuto, Nicolo'
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 1-gen-2002 Filosto, M.; Tonin, Paola; Vattemi, Gaetano Nicola; Spagnolo, M.; Rizzuto, Nicolo'; Tomelleri, Giuliano
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 1-gen-1998 Ferrari, Sergio; Morbin, M.; Nobile Orazio, E.; Musso, A.; Tomelleri, Giuliano; Bertolasi, Laura; Rizzuto, Nicolo'; Monaco, Salvatore
Ataxia and migraine-like headache in a girl with a cerebellar developmental venous anomaly 1-gen-2008 Fenzi, Flavio; Rizzuto, Nicolo'
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study. 1-gen-2006 Criscuolo, C; Chessa, L; DI GIANDOMENICO, S; Mancini, P; Sacca, F; Grieco, Gs; Piane, M; Barbieri, F; DE MICHELE, G; Banfi, S; Pierelli, F; Rizzuto, Nicolo'; Santorelli, Fm; Gallosti, L; Filla, A; Casali, C.