SALVADORI, CLAUDIO
SALVADORI, CLAUDIO
A new missense mutation in caveolin-3 gene causes rippling muscle disease.
2006-01-01 Dotti, Maria; Malandrini, Alessandro; Gambelli, Simona; Salvadori, Claudio; DE STEFANO, Nicola; Federico, Antonio
A syndrome of bilateral hemorrhage of the thalamus and myocarditis with fatal course.
2004-01-01 Malandrini, Alessandro; Luchini, D.; Gambelli, S.; Gaudiano, C.; Berti, Gianna; Salvadori, Claudio; Serni, Giovanni; Valassina, M.; Federico, Antonio; DI PAOLO, M.
Autonomic nervous system and smooth muscle cell invomvement in systemic sclerosis: ultrastructural study of three cases
2000-01-01 Malandrini, Alessandro; Selvi, E; Villanova, M; Berti, Gianna; Sabadini, L; Salvadori, Claudio; Gambelli, S; DE STEFANO, R; Vernillo, Remo; Marcolongo, FILIPPO ROBERTO; Guazzi, Gc
Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus.
1993-01-01 Malandrini, Alessandro; Fabrizi, Gm; Palmeri, Silvia; Ciacci, G; Salvadori, Claudio; Berti, Gianna; Bucalossi, A; Federico, Antonio; Guazzi, Gc
Gliomatosis cerebri with oligodendrocytic components: description of 1 case
2003-01-01 Palmeri, Silvia; Pompilio, A.; Ciacci, G.; Malandrini, Alessandro; Guazzi, Giancarlo; Rossi, Alessandro; Salvadori, Claudio; DI TROIA, A. M.; Spina, S.; Galluzzi, P.; Ginanneschi, Federica; Muzii, VITALIANO FRANCESCO; Schettini, G.; Miracco, Clelia; Soffietti, R.
Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report.
1998-01-01 Malandrini, Alessandro; Palmeri, Silvia; Fabrizi, Gm; Villanova, M; Berti, Gianna; Salvadori, Claudio; Gardini, G; Motti, L; Solimé, F; Guazzi, G. C.
Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy.
2004-01-01 Gambelli, S.; Malandrini, Alessandro; Ginanneschi, Federica; Berti, Gianna; Cardaioli, Elena; DE STEFANO, R.; Franci, M.; Salvadori, Claudio; Mari, Francesca; Bruttini, F.; Rossi, Alessandro; Federico, Antonio; Renieri, Alessandra
Neuronal intranuclear inclusion disease: neuropathologic study of a case.
1998-01-01 Malandrini, Alessandro; Villanova, M; Tripodi, S; Palmeri, Silvia; Sicurelli, F; Parrotta, E; Berti, Gianna; Salvadori, Claudio; Cintorino, M; Guazzi, G. C.
Neuropathological findings associated with retained lead shot pellets in a man surviving two months after a suicide attempt
2001-01-01 Malandrini, Alessandro; Villanova, MARCELLO PASQUALE; Salvadori, Claudio; Gambelli, Simona; Berti, Gianna; Di Paolo, M.
Typical pathological changes of CADASIL in the optic nerve.
2004-01-01 Rufa, Alessandra; Malandrini, Alessandro; Dotti, Maria; Formichi, Patrizia; Salvadori, Claudio; Federico, Antonio
Ultrastructural sperm abnormalities and cerebellar atrophy: does a correlation exist? Report of two cases without endocrine hypogonadism
1993-01-01 Malandrini, A.; Villanova, M.; Piomboni, P.; Collodel, G.; Spadaro, M.; Giunti, P.; Salvadori, C.; Morocutti, C.; Guazzi, G. C.
| Titolo | Data di pubblicazione | Autore(i) | File | Abstract |
|---|---|---|---|---|
| A new missense mutation in caveolin-3 gene causes rippling muscle disease. | 1-gen-2006 | Dotti, Maria; Malandrini, Alessandro; Gambelli, Simona; Salvadori, Claudio; DE STEFANO, Nicola; Federico, Antonio | - | |
| A syndrome of bilateral hemorrhage of the thalamus and myocarditis with fatal course. | 1-gen-2004 | Malandrini, Alessandro; Luchini, D.; Gambelli, S.; Gaudiano, C.; Berti, Gianna; Salvadori, Claudio; Serni, Giovanni; Valassina, M.; Federico, Antonio; DI PAOLO, M. | - | |
| Autonomic nervous system and smooth muscle cell invomvement in systemic sclerosis: ultrastructural study of three cases | 1-gen-2000 | Malandrini, Alessandro; Selvi, E; Villanova, M; Berti, Gianna; Sabadini, L; Salvadori, Claudio; Gambelli, S; DE STEFANO, R; Vernillo, Remo; Marcolongo, FILIPPO ROBERTO; Guazzi, Gc | - | |
| Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus. | 1-gen-1993 | Malandrini, Alessandro; Fabrizi, Gm; Palmeri, Silvia; Ciacci, G; Salvadori, Claudio; Berti, Gianna; Bucalossi, A; Federico, Antonio; Guazzi, Gc | - | |
| Gliomatosis cerebri with oligodendrocytic components: description of 1 case | 1-gen-2003 | Palmeri, Silvia; Pompilio, A.; Ciacci, G.; Malandrini, Alessandro; Guazzi, Giancarlo; Rossi, Alessandro; Salvadori, Claudio; DI TROIA, A. M.; Spina, S.; Galluzzi, P.; Ginanneschi, Federica; Muzii, VITALIANO FRANCESCO; Schettini, G.; Miracco, Clelia; Soffietti, R. | - | |
| Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report. | 1-gen-1998 | Malandrini, Alessandro; Palmeri, Silvia; Fabrizi, Gm; Villanova, M; Berti, Gianna; Salvadori, Claudio; Gardini, G; Motti, L; Solimé, F; Guazzi, G. C. | - | |
| Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy. | 1-gen-2004 | Gambelli, S.; Malandrini, Alessandro; Ginanneschi, Federica; Berti, Gianna; Cardaioli, Elena; DE STEFANO, R.; Franci, M.; Salvadori, Claudio; Mari, Francesca; Bruttini, F.; Rossi, Alessandro; Federico, Antonio; Renieri, Alessandra | - | |
| Neuronal intranuclear inclusion disease: neuropathologic study of a case. | 1-gen-1998 | Malandrini, Alessandro; Villanova, M; Tripodi, S; Palmeri, Silvia; Sicurelli, F; Parrotta, E; Berti, Gianna; Salvadori, Claudio; Cintorino, M; Guazzi, G. C. | - | |
| Neuropathological findings associated with retained lead shot pellets in a man surviving two months after a suicide attempt | 1-gen-2001 | Malandrini, Alessandro; Villanova, MARCELLO PASQUALE; Salvadori, Claudio; Gambelli, Simona; Berti, Gianna; Di Paolo, M. | - | |
| Typical pathological changes of CADASIL in the optic nerve. | 1-gen-2004 | Rufa, Alessandra; Malandrini, Alessandro; Dotti, Maria; Formichi, Patrizia; Salvadori, Claudio; Federico, Antonio | - | |
| Ultrastructural sperm abnormalities and cerebellar atrophy: does a correlation exist? Report of two cases without endocrine hypogonadism | 1-gen-1993 | Malandrini, A.; Villanova, M.; Piomboni, P.; Collodel, G.; Spadaro, M.; Giunti, P.; Salvadori, C.; Morocutti, C.; Guazzi, G. C. | - |