Sfoglia per Autore
Patogenesi biochimica della malattia di Leber
1986-01-01 Federico, A; Pallini, R; Bardelli, Am; Fabrizi, Gian Maria; Mangano, L; Manneschi, L; Dotti, Mt
Purification and characterization of UDP-Gal: Ceramide Galactosyltransferase and recostitution of its activity by incorporation into liposomes.
1987-01-01 Berardi, A; Fabrizi, Gian Maria; Manetti, R; Costantino Ceccarini, E.
The Italian hemodilution trial in acute stroke.
1987-01-01 Fabrizi, Gian Maria
Headache, seizures and repente strokes in a young subject: a new case of MELAS-like syndrome?
1988-01-01 Fabrizi, Gian Maria; Manneschi, L.; Marcacci, G.; Volpi, N.; Sabatelli, P.; Guazzi, G. C.; Federico, A.
Rubinstein-Taybi syndrome. Report of two cases.
1988-01-01 Ciacci, G.; D'Amore, I.; Fabrizi, Gian Maria; Rocchi, R.; Volpi, N.; Federico, A.
Haemodilution in acute stroke: results of the Italian haemodilution trial.
1988-01-01 Italian Acute Stroke Study, Group; Fabrizi, Gian Maria
Mitochondrial encephalo-neuro-myopathy with myoclonus epilepsy, basal nuclei calcification and hyperlactacidemia.
1988-01-01 Federico, A.; Cornelio, F.; Di Donato, S.; Ederli, E.; Fabrizi, Gian Maria; Manneschi, L.; Guazzi, G. C.
Patologia oculare nelle encefalo-neuro-miopatie genetiche mitocondriali.
1989-01-01 Fabrizi, Gian Maria; Dotti, Mt; Federico, A; Guazzi, Gc
Isolamento di cloni di cDNA per le subunità VIa e VIIa della Citocromo c ossidasi umana (COX).
1989-01-01 Fabrizi, Gian Maria; Schon, E. A.
A gene specifying subunit VIII of human cytochrome c oxidase is localized to chromosome 11 and is expressed in both muscle and non-muscle tissues.
1989-01-01 Rizzuto, R.; Nakase, H.; Darras, B.; Francke, U.; Fabrizi, Gian Maria; Mengel, T.; Walsh, F.; Kadenback, B.; Dimauro, S.; Schon, E. A.
Sequence of a cDNA specifying subunit VIIa of human cytochrome c oxidase.
1989-01-01 Fabrizi, Gian Maria; Rizzuto, R.; Nakase, H.; Mita, S.; Lomax, M. I.; Grossman, L. I.; Schon, E. A.
Sequence of a cDNA specifying subunit VIa of human cytochrome c oxidase.
1989-01-01 Fabrizi, Gian Maria; Rizzuto, R.; Nakase, H.; Mita, S.; Kadenbach, B.; Schon, E. A.
Correlazioni cliniche, biochimiche e molecolari in 15 casi di Oftalmoplegia cronica progressiva
1990-01-01 Fabrizi, Gian Maria; Eusebi, Mp; Siciliano, G; Rossi, B; Volpi, N; Federico, A.
The strategy of investigating autistic syndrome in childhood.
1990-01-01 Federico, A.; Battistini, S.; De Stefano, N.; Eusebi, M. P.; Fabrizi, Gian Maria; Dotti, M. T.
Eterogeneità genetico molecolare della neuropatia ottica ereditaria di Leber
1990-01-01 Fabrizi, Gian Maria; Dotti, M. T.; Federico, A.
Cytochrome c oxidase deficiency.
1990-01-01 Dlmauro, S.; Lombes, A.; Nakase, H.; Mita, S.; Fabrizi, G. M.; Tritschler, H. -J.; Bonilla, E.; Miranda, A. F.; Devivo, D. C.; Schon, E. A.
Recombination via flanking direct repeats is a major casue of large-scale deletions of human mitochondrial DNA
1990-01-01 Mita, S.; Rizzuto, R.; Moraes, C. T.; Shanske, S.; Arnaudo, E.; Fabrizi, G. M.; Koga, Y.; Dimauro, S.; Schon, E. A.
Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy.
1990-01-01 Federico, A.; Dotti, M. T.; Fabrizi, G. M.; Paimeri, S.; Massimo, L.; Robinson, B. H.; Malandrini, A.; Guazzi, G. C.
Sequence of a cDNA specifying subunit VIIc of human cytochrome c oxidase
1990-01-01 Koga, Y.; Fabrizi, G. M.; Mita, S.; Arnaudo, E.; Lomax, M. I.; Aqua, M. S.; Grossman, L. I.; Schon, E. A.
Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti.
1990-01-01 Federico, A.; Fabrizi, Gian Maria; Dotti, M. T.; Palmeri, S.; Aguglia, U; Miracco, C.; Guazzi, G. C.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Patogenesi biochimica della malattia di Leber | 1-gen-1986 | Federico, A; Pallini, R; Bardelli, Am; Fabrizi, Gian Maria; Mangano, L; Manneschi, L; Dotti, Mt | |
| Purification and characterization of UDP-Gal: Ceramide Galactosyltransferase and recostitution of its activity by incorporation into liposomes. | 1-gen-1987 | Berardi, A; Fabrizi, Gian Maria; Manetti, R; Costantino Ceccarini, E. | |
| The Italian hemodilution trial in acute stroke. | 1-gen-1987 | Fabrizi, Gian Maria | |
| Headache, seizures and repente strokes in a young subject: a new case of MELAS-like syndrome? | 1-gen-1988 | Fabrizi, Gian Maria; Manneschi, L.; Marcacci, G.; Volpi, N.; Sabatelli, P.; Guazzi, G. C.; Federico, A. | |
| Rubinstein-Taybi syndrome. Report of two cases. | 1-gen-1988 | Ciacci, G.; D'Amore, I.; Fabrizi, Gian Maria; Rocchi, R.; Volpi, N.; Federico, A. | |
| Haemodilution in acute stroke: results of the Italian haemodilution trial. | 1-gen-1988 | Italian Acute Stroke Study, Group; Fabrizi, Gian Maria | |
| Mitochondrial encephalo-neuro-myopathy with myoclonus epilepsy, basal nuclei calcification and hyperlactacidemia. | 1-gen-1988 | Federico, A.; Cornelio, F.; Di Donato, S.; Ederli, E.; Fabrizi, Gian Maria; Manneschi, L.; Guazzi, G. C. | |
| Patologia oculare nelle encefalo-neuro-miopatie genetiche mitocondriali. | 1-gen-1989 | Fabrizi, Gian Maria; Dotti, Mt; Federico, A; Guazzi, Gc | |
| Isolamento di cloni di cDNA per le subunità VIa e VIIa della Citocromo c ossidasi umana (COX). | 1-gen-1989 | Fabrizi, Gian Maria; Schon, E. A. | |
| A gene specifying subunit VIII of human cytochrome c oxidase is localized to chromosome 11 and is expressed in both muscle and non-muscle tissues. | 1-gen-1989 | Rizzuto, R.; Nakase, H.; Darras, B.; Francke, U.; Fabrizi, Gian Maria; Mengel, T.; Walsh, F.; Kadenback, B.; Dimauro, S.; Schon, E. A. | |
| Sequence of a cDNA specifying subunit VIIa of human cytochrome c oxidase. | 1-gen-1989 | Fabrizi, Gian Maria; Rizzuto, R.; Nakase, H.; Mita, S.; Lomax, M. I.; Grossman, L. I.; Schon, E. A. | |
| Sequence of a cDNA specifying subunit VIa of human cytochrome c oxidase. | 1-gen-1989 | Fabrizi, Gian Maria; Rizzuto, R.; Nakase, H.; Mita, S.; Kadenbach, B.; Schon, E. A. | |
| Correlazioni cliniche, biochimiche e molecolari in 15 casi di Oftalmoplegia cronica progressiva | 1-gen-1990 | Fabrizi, Gian Maria; Eusebi, Mp; Siciliano, G; Rossi, B; Volpi, N; Federico, A. | |
| The strategy of investigating autistic syndrome in childhood. | 1-gen-1990 | Federico, A.; Battistini, S.; De Stefano, N.; Eusebi, M. P.; Fabrizi, Gian Maria; Dotti, M. T. | |
| Eterogeneità genetico molecolare della neuropatia ottica ereditaria di Leber | 1-gen-1990 | Fabrizi, Gian Maria; Dotti, M. T.; Federico, A. | |
| Cytochrome c oxidase deficiency. | 1-gen-1990 | Dlmauro, S.; Lombes, A.; Nakase, H.; Mita, S.; Fabrizi, G. M.; Tritschler, H. -J.; Bonilla, E.; Miranda, A. F.; Devivo, D. C.; Schon, E. A. | |
| Recombination via flanking direct repeats is a major casue of large-scale deletions of human mitochondrial DNA | 1-gen-1990 | Mita, S.; Rizzuto, R.; Moraes, C. T.; Shanske, S.; Arnaudo, E.; Fabrizi, G. M.; Koga, Y.; Dimauro, S.; Schon, E. A. | |
| Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy. | 1-gen-1990 | Federico, A.; Dotti, M. T.; Fabrizi, G. M.; Paimeri, S.; Massimo, L.; Robinson, B. H.; Malandrini, A.; Guazzi, G. C. | |
| Sequence of a cDNA specifying subunit VIIc of human cytochrome c oxidase | 1-gen-1990 | Koga, Y.; Fabrizi, G. M.; Mita, S.; Arnaudo, E.; Lomax, M. I.; Aqua, M. S.; Grossman, L. I.; Schon, E. A. | |
| Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti. | 1-gen-1990 | Federico, A.; Fabrizi, Gian Maria; Dotti, M. T.; Palmeri, S.; Aguglia, U; Miracco, C.; Guazzi, G. C. |
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