Sfoglia per Autore
Cytoskeletal pathology in ataxia-telangiectasia.
1988-01-01 Monaco, Salvatore; E., Nardelli; G., Moretto; Cavallaro, Tiziana; Rizzuto, Nicolo'
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats.
1989-01-01 Simonati, Alessandro; Monaco, Salvatore; Cavallaro, Tiziana; Rizzuto, Nicolo'
La patologia delle neuropatie periferiche.
1994-01-01 Cavallaro, Tiziana; Morbin, M.; Ferrari, Sergio; Simonati, Alessandro; Rizzuto, Nicolo'
Neuropatie immunitarie.
1994-01-01 Ferrari, Sergio; Bonetti, Bruno; Monaco, Salvatore; Cavallaro, Tiziana; Morbin, M.; Simonati, Alessandro; Rizzuto, Nicolo'
Neuropatie genetiche.
1994-01-01 Simonati, Alessandro; Cavallaro, Tiziana; Ferrari, Sergio; Morbin, M.; Rizzuto, Nicolo'
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy
1995-01-01 Rizzuto, Nicolo'; Cavallaro, Tiziana; Monaco, Salvatore; Morbin, M.; Bonetti, Bruno; Ferrari, Sergio; Galiazzo Rizzuto, S.; Zanette, G.; Bertolasi, Laura
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy.
1995-01-01 Malandrini, A.; Cavallaro, T.; Fabrizi, G. M.; Berti, G.; Salvestroni, R.; Salvadori, C.; Guazzi, G. C.
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy
1996-01-01 Malandrini, A.; Carrera, P.; Palmeri, S.; Cavallaro, T.; Fabrizi, Gian Maria; Villanova, M.; Fattaposta, M.; Vismara, L.; Brancolini, V.; Tanganelli, P.; Cali, A.; Morocutti, C.; Zeviani, M.; Ferrari, M.; Guazzi, G. C.
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome.
1996-01-01 Fabrizi, Gian Maria; Cardaioli, E.; Grieco, G. S.; Cavallaro, Tiziana; Malandrini, A.; Manneschi, L.; Dotti, M. T.; Federico, A.; Guazzi, G. C.
Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a mutlisystem mitochondrial defect.
1996-01-01 Fabrizi, Gian Maria; Lodi, R.; D'Ettorre, M.; Malandrini, A.; Cavallaro, Tiziana; Rimoldi, M.; Zaniol, P.; Barbiroli, B.; Guazzi, G. C.
Neuronal intranuclear inclusion disease: Polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case
1996-01-01 Malandrini, A.; Fabrizi, G. M.; Cavallaro, T.; Zazzi, M.; Parrotta, E.; Romano, L.; Berti, G.; Villanova, M.; Guazzi, G. C.
Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP).
1998-01-01 Rizzuto, Nicolo'; Morbin, M.; Cavallaro, Tiziana; Ferrari, Sergio; Fallahi, M.; GALIAZZO RIZZUTO, S.
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases
1998-01-01 Fabrizi, Gian Maria; Simonati, Alessandro; Morbin, M.; Cavallaro, T.; Taioli, Federica; Benedetti, M. D.; Edomi, P.; Rizzuto, Nicolo'
Clinical and pathological findings in HCV-related peripheral neuropathies
1999-01-01 Nardelli, Ettore; Bonetti, Bruno; Cavallaro, Tiziana
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome
1999-01-01 Fabrizi, Gian Maria; Cavallaro, T.; Morbin, M.; Simonati, Alessandro; Taioli, Federica; Rizzuto, Nicolo'
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22
1999-01-01 Simonati, Alessandro; Fabrizi, Gian Maria; Pasquinelli, A.; Taioli, Federica; Cavallaro, T.; Morbin, M.; Marcon, G.; Papini, M.; Rizzuto, Nicolo'
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22
1999-01-01 Fabrizi, Gian Maria; Cavallaro, T.; Taioli, Federica; Orrico, D.; Morbin, M.; Simonati, Alessandro; Rizzuto, Nicolo'
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32
2000-01-01 Fabrizi, Gian Maria; A., Polo; Cavallaro, Tiziana; C., Pinardi; Taioli, Federica; C., Corrà; Rizzuto, Nicolo'
Congenital hypomyelination neuropathy with a novel mutation of PMP22
2000-01-01 Rigatelli, F.; Fabrizi, Gian Maria; Simonati, Alessandro; Cavallaro, Tiziana; Ferrarini, Moreno; Taioli, Federica; Mostacciuolo, M. L.; Rizzuto, Nicolo'
I quadri neuropatologici delle sindromi paraneoplastiche
2000-01-01 Rizzuto, Nicolo'; Cavallaro, Tiziana; Fabrizi, Gian Maria
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Cytoskeletal pathology in ataxia-telangiectasia. | 1-gen-1988 | Monaco, Salvatore; E., Nardelli; G., Moretto; Cavallaro, Tiziana; Rizzuto, Nicolo' | |
| Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. | 1-gen-1989 | Simonati, Alessandro; Monaco, Salvatore; Cavallaro, Tiziana; Rizzuto, Nicolo' | |
| La patologia delle neuropatie periferiche. | 1-gen-1994 | Cavallaro, Tiziana; Morbin, M.; Ferrari, Sergio; Simonati, Alessandro; Rizzuto, Nicolo' | |
| Neuropatie immunitarie. | 1-gen-1994 | Ferrari, Sergio; Bonetti, Bruno; Monaco, Salvatore; Cavallaro, Tiziana; Morbin, M.; Simonati, Alessandro; Rizzuto, Nicolo' | |
| Neuropatie genetiche. | 1-gen-1994 | Simonati, Alessandro; Cavallaro, Tiziana; Ferrari, Sergio; Morbin, M.; Rizzuto, Nicolo' | |
| Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy | 1-gen-1995 | Rizzuto, Nicolo'; Cavallaro, Tiziana; Monaco, Salvatore; Morbin, M.; Bonetti, Bruno; Ferrari, Sergio; Galiazzo Rizzuto, S.; Zanette, G.; Bertolasi, Laura | |
| Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. | 1-gen-1995 | Malandrini, A.; Cavallaro, T.; Fabrizi, G. M.; Berti, G.; Salvestroni, R.; Salvadori, C.; Guazzi, G. C. | |
| Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy | 1-gen-1996 | Malandrini, A.; Carrera, P.; Palmeri, S.; Cavallaro, T.; Fabrizi, Gian Maria; Villanova, M.; Fattaposta, M.; Vismara, L.; Brancolini, V.; Tanganelli, P.; Cali, A.; Morocutti, C.; Zeviani, M.; Ferrari, M.; Guazzi, G. C. | |
| The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause a MERFF syndrome. | 1-gen-1996 | Fabrizi, Gian Maria; Cardaioli, E.; Grieco, G. S.; Cavallaro, Tiziana; Malandrini, A.; Manneschi, L.; Dotti, M. T.; Federico, A.; Guazzi, G. C. | |
| Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a mutlisystem mitochondrial defect. | 1-gen-1996 | Fabrizi, Gian Maria; Lodi, R.; D'Ettorre, M.; Malandrini, A.; Cavallaro, Tiziana; Rimoldi, M.; Zaniol, P.; Barbiroli, B.; Guazzi, G. C. | |
| Neuronal intranuclear inclusion disease: Polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case | 1-gen-1996 | Malandrini, A.; Fabrizi, G. M.; Cavallaro, T.; Zazzi, M.; Parrotta, E.; Romano, L.; Berti, G.; Villanova, M.; Guazzi, G. C. | |
| Focal lesions are a feature of chronic inflammatory demyelinating polyneuropathy (CIDP). | 1-gen-1998 | Rizzuto, Nicolo'; Morbin, M.; Cavallaro, Tiziana; Ferrari, Sergio; Fallahi, M.; GALIAZZO RIZZUTO, S. | |
| Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases | 1-gen-1998 | Fabrizi, Gian Maria; Simonati, Alessandro; Morbin, M.; Cavallaro, T.; Taioli, Federica; Benedetti, M. D.; Edomi, P.; Rizzuto, Nicolo' | |
| Clinical and pathological findings in HCV-related peripheral neuropathies | 1-gen-1999 | Nardelli, Ettore; Bonetti, Bruno; Cavallaro, Tiziana | |
| Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome | 1-gen-1999 | Fabrizi, Gian Maria; Cavallaro, T.; Morbin, M.; Simonati, Alessandro; Taioli, Federica; Rizzuto, Nicolo' | |
| Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 | 1-gen-1999 | Simonati, Alessandro; Fabrizi, Gian Maria; Pasquinelli, A.; Taioli, Federica; Cavallaro, T.; Morbin, M.; Marcon, G.; Papini, M.; Rizzuto, Nicolo' | |
| Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 | 1-gen-1999 | Fabrizi, Gian Maria; Cavallaro, T.; Taioli, Federica; Orrico, D.; Morbin, M.; Simonati, Alessandro; Rizzuto, Nicolo' | |
| X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 | 1-gen-2000 | Fabrizi, Gian Maria; A., Polo; Cavallaro, Tiziana; C., Pinardi; Taioli, Federica; C., Corrà; Rizzuto, Nicolo' | |
| Congenital hypomyelination neuropathy with a novel mutation of PMP22 | 1-gen-2000 | Rigatelli, F.; Fabrizi, Gian Maria; Simonati, Alessandro; Cavallaro, Tiziana; Ferrarini, Moreno; Taioli, Federica; Mostacciuolo, M. L.; Rizzuto, Nicolo' | |
| I quadri neuropatologici delle sindromi paraneoplastiche | 1-gen-2000 | Rizzuto, Nicolo'; Cavallaro, Tiziana; Fabrizi, Gian Maria |
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