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Glutathione, glutathione utilizing enzymes and thioltransferase in platelets of insulin-dependent diabetic patients: relation with platelet aggregation and with microangiopatic complications. [electronic resource] by
- Di Simplicio, P
- de Giorgio, L A
- Cardaioli, E
- Lecis, R
- Miceli, M
- Rossi, R
- Anichini, R
- Mian, M
- Seghieri, G
- Franconi, F
Producer: 19960117
In:
European journal of clinical investigation vol. 25
Availability: No items available.
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12.
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Genetic leukoencephalopathies with unknown metabolic pathogenesis. [electronic resource] by
- Federico, A
- Rufa, A
- Battisti, C
- Bianchi, S
- Cardaioli, E
- Da Pozzo, P
- De Stefano, N
- Formichi, P
- Sicurelli, F
- Dotti, M T
Producer: 20020626
In:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 22 Suppl 2
Availability: No items available.
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13.
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The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene. [electronic resource] by
- Szlago, M
- Gallus, G N
- Schenone, A
- Patiño, M E
- Sfaelo, Z
- Rufa, A
- Da Pozzo, P
- Cardaioli, E
- Dotti, M T
- Federico, A
Producer: 20080229
In:
Neurology vol. 70
Availability: No items available.
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14.
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Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study. [electronic resource] by
- Federico, A
- Dotti, M T
- Cardaioli, E
- Grieco, G
- Malandrini, A
- Manneschi, L
- Plewnia, K
- Rufa, A
- Renieri, A
- Bruttini, M
- Perticoni, G F
Producer: 19990104
In:
Journal of submicroscopic cytology and pathology vol. 30
Availability: No items available.
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15.
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Chronic progressive external ophthalmoplegia: a new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNA. [electronic resource] by
- Cardaioli, E
- Da Pozzo, P
- Malfatti, E
- Gallus, G N
- Rubegni, A
- Malandrini, A
- Gaudiano, C
- Guidi, L
- Serni, G
- Berti, G
- Dotti, M T
- Federico, A
Producer: 20081218
In:
Journal of the neurological sciences vol. 272
Availability: No items available.
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16.
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Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy. [electronic resource] by
- Gambelli, S
- Malandrini, A
- Ginanneschi, F
- Berti, G
- Cardaioli, E
- De Stefano, R
- Franci, M
- Salvadori, C
- Mari, F
- Bruttini, M
- Rossi, A
- Federico, A
- Renieri, A
Producer: 20040615
In:
European neurology vol. 51
Availability: No items available.
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17.
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Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-up. [electronic resource] by
- Sicurelli, F
- Carluccio, M A
- Toraldo, F
- Tozzi, M
- Bucalossi, A
- Lenoci, M
- Jacomelli, G
- Micheli, V
- Cardaioli, E
- Mondelli, M
- Federico, A
- Marotta, G
- Dotti, M T
Producer: 20130128
In:
Journal of neurology vol. 259
Availability: No items available.
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18.
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Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families. [electronic resource] by
- Pretegiani, E
- Rosini, F
- Rufa, A
- Gallus, G N
- Cardaioli, E
- Da Pozzo, P
- Bianchi, S
- Serchi, V
- Collura, M
- Franceschini, R
- Bianchi Marzoli, S
- Dotti, M T
- Federico, A
Producer: 20180621
In:
Journal of the neurological sciences vol. 382
Availability: No items available.
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19.
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Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family. [electronic resource] by
- Casali, C
- Fabrizi, G M
- Santorelli, F M
- Colazza, G
- Villanova, M
- Dotti, M T
- Cavallaro, T
- Cardaioli, E
- Battisti, C
- Manneschi, L
- DiGennaro, G C
- Fortini, D
- Spadaro, M
- Morocutti, C
- Federico, A
Producer: 19990506
In:
Neurology vol. 52
Availability: No items available.
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