Sfoglia per Autore
The clinical aspects of adult hexosaminidase deficiencies
1991-01-01 Federico, A.; Palmeri, S.; Malandrini, A.; Fabrizi, Gian Maria; Mondelli, M.; Guazzi, G. C.
Mortality in acute stroke with atrial fibrillation. The Italian Acute Stroke Study Group.
1991-01-01 Candelise, L.; Pinardi, G.; Morabito, A.; Fabrizi, Gian Maria
L'enigma genetico della neuropatia ottica di Leber e della neurofibromatosi di Recklinghausen
1992-01-01 Bardelli, Am; Federico, A; Traversi, C; Fabrizi, Gian Maria
Late onset mitochondrial encephalo-neuro-myopathies
1992-01-01 Federico, A; Battistini, S; De STefano, N; Dotti, Mt; Eusebi, Mp; Fabrizi, Gian Maria; Malandrini, A; Manneschi, A; Guazzi, G. C.
Mutazioni del DNA mitocondriale nella neuropatia ottica di Leber
1992-01-01 Fabrizi, Gian Maria; De STefano, N; Dotti, Mt; Federico, A; Mondelli, M; Traversi, C; Vanni, M; Guazzi, G. C.
Variability of the expression of muscle mitochondrial damage in ocular mitochondrial myopathy
1992-01-01 Siciliano, G.; Rossi, B.; Angelini, C.; Martinuzzi, A.; Carrozzo, R.; Bevilacqua, G.; Viacava, P.; Federico, A.; Fabrizi, G. M.; Muratorio, A.
Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase
1992-01-01 Arnaudo, E.; Hirano, M.; Sedan, R. S.; Milatovich, A.; Hsieh, C. -L.; Fabrizi, G. M.; Grossman, L. I.; Francke, U.; Schon, E. A.
Differential expression of genes specifying two isoforms of subunit VIa of human cytochrome c oxidase
1992-01-01 Fabrizi, G. M.; Sadlock, J.; Hirano, M.; Mita, S.; Koga, Y.; Rizzuto, R.; Zeviani, M.; Schon, E. A.
Modificazioni del DNA mitocondriale nella neuropatia ottica di Leber.
1993-01-01 Fabrizi, Gian Maria; Bardelli, Am; De Stefano, N; Dotti, Mt; Federico, A; Mondelli, M; Traversi, C; Guazzi, G. C.
Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expression.
1993-01-01 Dotti, M. T.; Malandrini, A.; Bartolini, S.; Fabrizi, G. M.; Federico, A.
Choreo-acanthocytosis like phenotype without acanthocytoses: clinico-pathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus.
1993-01-01 Malandrini, A.; Fabrizi, G. M.; Palmeri, S.; Ciacci, G.; Salvadori, C.; Berti, G.; Bucalossi, A.; Federico, A.; Guazzi, G. C.
La patologia della sostanza bianca alla RM osservata da un clinico.
1994-01-01 Guazzi, Gc; Fabrizi, Gian Maria; Malandrini, A.
Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family.
1994-01-01 Malandrini, A.; Fabrizi, G. M.; Truschi, F.; Di Pietro, G.; Moschini, F.; Bartalucci, P.; Berti, G.; Salvadori, C.; Bucalossi, A.; Guazzi, G. C.
Studio clinico, neuroradiologico e neuropatologico di due famiglie con arteriopatia cerebrale autosomica dominante.
1995-01-01 Malandrini, A; Palmeri, S; Cavallaro, T; Fabrizi, Gian Maria; Villanova, M; Fattaposta, M; Morocutti, C; Guazzi, G. C.
Aggressive treatment of severe acute cerebral venous thrombosis associated with oral contraceptives in young women
1995-01-01 Rosi, R.; Stanca, A.; Monfregola, Mr; Malandrini, A.; Fabrizi, Gian Maria; Galluzzi, P.; Filosomi, G.
Mitochondrial changes in steroid myopathy with respiratory failure and rapid fatal course: report of a case.
1995-01-01 Malandrini, A.; Scarpini, C.; Fabrizi, Gian Maria; Manneschi, L.; Rosi, R.; Parrotta, E.; Guazzi, G. C.
Early-onset benign limb-girdle myopathy with contractures and facial involvement affecting a father and daughter.
1995-01-01 Malandrini, A.; Scarpini, C.; Fabrizi, Gian Maria; Parrotta, E.; Salvadori, C.; Guazzi, G. C.
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.
Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy
1995-01-01 Fabrizi, G. M.; Guazzi, G. C.; Malandrini, A.; Tiranti, V.; Mariotti, C.; Di Donato, S.; Zeviani, M.
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.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| The clinical aspects of adult hexosaminidase deficiencies | 1-gen-1991 | Federico, A.; Palmeri, S.; Malandrini, A.; Fabrizi, Gian Maria; Mondelli, M.; Guazzi, G. C. | |
| Mortality in acute stroke with atrial fibrillation. The Italian Acute Stroke Study Group. | 1-gen-1991 | Candelise, L.; Pinardi, G.; Morabito, A.; Fabrizi, Gian Maria | |
| L'enigma genetico della neuropatia ottica di Leber e della neurofibromatosi di Recklinghausen | 1-gen-1992 | Bardelli, Am; Federico, A; Traversi, C; Fabrizi, Gian Maria | |
| Late onset mitochondrial encephalo-neuro-myopathies | 1-gen-1992 | Federico, A; Battistini, S; De STefano, N; Dotti, Mt; Eusebi, Mp; Fabrizi, Gian Maria; Malandrini, A; Manneschi, A; Guazzi, G. C. | |
| Mutazioni del DNA mitocondriale nella neuropatia ottica di Leber | 1-gen-1992 | Fabrizi, Gian Maria; De STefano, N; Dotti, Mt; Federico, A; Mondelli, M; Traversi, C; Vanni, M; Guazzi, G. C. | |
| Variability of the expression of muscle mitochondrial damage in ocular mitochondrial myopathy | 1-gen-1992 | Siciliano, G.; Rossi, B.; Angelini, C.; Martinuzzi, A.; Carrozzo, R.; Bevilacqua, G.; Viacava, P.; Federico, A.; Fabrizi, G. M.; Muratorio, A. | |
| Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase | 1-gen-1992 | Arnaudo, E.; Hirano, M.; Sedan, R. S.; Milatovich, A.; Hsieh, C. -L.; Fabrizi, G. M.; Grossman, L. I.; Francke, U.; Schon, E. A. | |
| Differential expression of genes specifying two isoforms of subunit VIa of human cytochrome c oxidase | 1-gen-1992 | Fabrizi, G. M.; Sadlock, J.; Hirano, M.; Mita, S.; Koga, Y.; Rizzuto, R.; Zeviani, M.; Schon, E. A. | |
| Modificazioni del DNA mitocondriale nella neuropatia ottica di Leber. | 1-gen-1993 | Fabrizi, Gian Maria; Bardelli, Am; De Stefano, N; Dotti, Mt; Federico, A; Mondelli, M; Traversi, C; Guazzi, G. C. | |
| Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expression. | 1-gen-1993 | Dotti, M. T.; Malandrini, A.; Bartolini, S.; Fabrizi, G. M.; Federico, A. | |
| Choreo-acanthocytosis like phenotype without acanthocytoses: clinico-pathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus. | 1-gen-1993 | Malandrini, A.; Fabrizi, G. M.; Palmeri, S.; Ciacci, G.; Salvadori, C.; Berti, G.; Bucalossi, A.; Federico, A.; Guazzi, G. C. | |
| La patologia della sostanza bianca alla RM osservata da un clinico. | 1-gen-1994 | Guazzi, Gc; Fabrizi, Gian Maria; Malandrini, A. | |
| Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family. | 1-gen-1994 | Malandrini, A.; Fabrizi, G. M.; Truschi, F.; Di Pietro, G.; Moschini, F.; Bartalucci, P.; Berti, G.; Salvadori, C.; Bucalossi, A.; Guazzi, G. C. | |
| Studio clinico, neuroradiologico e neuropatologico di due famiglie con arteriopatia cerebrale autosomica dominante. | 1-gen-1995 | Malandrini, A; Palmeri, S; Cavallaro, T; Fabrizi, Gian Maria; Villanova, M; Fattaposta, M; Morocutti, C; Guazzi, G. C. | |
| Aggressive treatment of severe acute cerebral venous thrombosis associated with oral contraceptives in young women | 1-gen-1995 | Rosi, R.; Stanca, A.; Monfregola, Mr; Malandrini, A.; Fabrizi, Gian Maria; Galluzzi, P.; Filosomi, G. | |
| Mitochondrial changes in steroid myopathy with respiratory failure and rapid fatal course: report of a case. | 1-gen-1995 | Malandrini, A.; Scarpini, C.; Fabrizi, Gian Maria; Manneschi, L.; Rosi, R.; Parrotta, E.; Guazzi, G. C. | |
| Early-onset benign limb-girdle myopathy with contractures and facial involvement affecting a father and daughter. | 1-gen-1995 | Malandrini, A.; Scarpini, C.; Fabrizi, Gian Maria; Parrotta, E.; Salvadori, C.; Guazzi, G. C. | |
| 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. | |
| Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy | 1-gen-1995 | Fabrizi, G. M.; Guazzi, G. C.; Malandrini, A.; Tiranti, V.; Mariotti, C.; Di Donato, S.; Zeviani, M. | |
| 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. |
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