FEDERICO, ANTONIO
FEDERICO, ANTONIO
Dipartimento di Scienze Mediche, Chirurgiche e Neuroscienze
"Mitochondrial neuropathies": A survey from the large cohort of the Italian Network
2016-01-01 Mancuso, Michelangelo; Orsucci, Daniele; Angelini, Corrado; Bertini, Enrico; Carelli, Valerio; Comi, Giacomo Pietro; Federico, Antonio; Minetti, Carlo; Moggio, Maurizio; Mongini, Tiziana; Tonin, Paola; Toscano, Antonio; Bruno, Claudio; Ienco, Elena Caldarazzo; Filosto, Massimiliano; Lamperti, Costanza; Diodato, Daria; Moroni, Isabella; Musumeci, Olimpia; Pegoraro, Elena; Spinazzi, Marco; Ahmed, Naghia; Sciacco, Monica; Vercelli, Liliana; Ardissone, Anna; Zeviani, Massimo; Siciliano, Gabriele
1H-MR Spectroscopy in Traumatic Brain Injury
2011-01-01 Marino, S; Ciurleo, R; Bramanti, P; Federico, Antonio; DE STEFANO, Nicola
[Biochemical diagnosis of subacute and chronic neuropathies].
1984-01-01 Federico, Antonio
[Cerebrotendinous xanthomatosis. A case report].
1996-01-01 Sabadini, L; Gonnelli, L; Anichini, C; Funtò, I; Marcolongo, R; Dotti, Mg; Federico, Antonio
[Complications and safety in the use of hyperbaric subarachnoid anesthesia in aged patients].
1982-01-01 Federico, Antonio; Ciccolo, F.
[Italian neurology: past, present and future.]
2011-01-01 Federico, Antonio
[Multiple sclerosis. Etiopathogenetic review].
1975-01-01 Federico, Antonio
[Rubinstein-Taybi syndrome with multiple keloids].
1986-01-01 Sammartino, A; Cerbella, R; Lembo, G; Federico, Antonio; Loffredo, L.
A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies.
2009-01-01 Rosini, Francesca; Pretegiani, Elena; D., Donati; D., Moschettini; Rubegni, Anna; Rufa, Alessandra; Annunziata, Pasquale; Federico, Antonio
A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia.
2014-01-01 Rubegni, A; Cardaioli, Elena; Chini, Elena; DA POZZO, Paola; Battisti, Carla; Malandrini, Alessandro; Federico, Antonio
A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE
2010-01-01 Mignarri, Andrea; M., Falcini; Gallus, GIAN NICOLA; Giorgio, Antonio; Rufa, Alessandra; Ginanneschi, Federica; Federico, Antonio; Dotti, Maria
A case of dystonia with onset during pregnancy.
2007-01-01 Buccoliero, R; Palmeri, Silvia; Malandrini, Alessandro; Dotti, Maria; Federico, Antonio
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778.
1998-01-01 Dotti, Maria; Plewnia, K; Cardaioli, Elena; Manneschi, L; Rufa, Alessandra; Alemà, G; Federico, Antonio
A case of ovarioleukodystrophy without elF2B mutations.
2008-01-01 Gaudiano, C; DI PERRI, C; Scali, O; Rufa, Alessandra; Battisti, Carla; DE STEFANO, Nicola; Federico, Antonio
A case report of transient posterior internuclear ophthalmoplegia (PINO) associated with encephalitis of ponto-mesencephalic junction
2007-01-01 Buccoliero, R; Rufa, Alessandra; A., Cerase; L., Monti; Malandrini, Alessandro; Federico, Antonio
A new case of short-chain acyl-CoA dehydrogenase deficiency: clinical, biochemical, genetic and (1)H-NMR spectroscopic studies.
2007-01-01 Battisti, C; Forte, F; Molinelli, MASSIMO CLAUDIO; Funghini, S; Pasquini, E; Tassini, M; Dotti, Maria; Federico, Antonio
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes.
2005-01-01 Sperduto, A; Dotti, Maria; DE STEFANO, Nicola; De Santis, M; Bianchi, Silvia; Rufa, Alessandra; Frantellizzi, P; Federico, Antonio
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 new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy
2012-01-01 Cardaioli, Elena; Sicurelli, F; Carluccio, MARIA ALESSANDRA; Gallus, GIAN NICOLA; DA POZZO, Paola; Mondelli, M; Margollicci, Ma; Micheli, V; Federico, Antonio; Dotti, Maria
A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
2015-01-01 DI DONATO, Ilaria; Stabile, Carmen; Bianchi, Silvia; Taglia, Ilaria; Mignarri, Andrea; Salvatore, Simona; Giorgio, Elisa; Brusco, Alfredo; Simone, Isabella; Dotti, Maria; Federico, Antonio
| Titolo | Data di pubblicazione | Autore(i) | File | Abstract |
|---|---|---|---|---|
| "Mitochondrial neuropathies": A survey from the large cohort of the Italian Network | 1-gen-2016 | Mancuso, Michelangelo; Orsucci, Daniele; Angelini, Corrado; Bertini, Enrico; Carelli, Valerio; Comi, Giacomo Pietro; Federico, Antonio; Minetti, Carlo; Moggio, Maurizio; Mongini, Tiziana; Tonin, Paola; Toscano, Antonio; Bruno, Claudio; Ienco, Elena Caldarazzo; Filosto, Massimiliano; Lamperti, Costanza; Diodato, Daria; Moroni, Isabella; Musumeci, Olimpia; Pegoraro, Elena; Spinazzi, Marco; Ahmed, Naghia; Sciacco, Monica; Vercelli, Liliana; Ardissone, Anna; Zeviani, Massimo; Siciliano, Gabriele | - | |
| 1H-MR Spectroscopy in Traumatic Brain Injury | 1-gen-2011 | Marino, S; Ciurleo, R; Bramanti, P; Federico, Antonio; DE STEFANO, Nicola | - | |
| [Biochemical diagnosis of subacute and chronic neuropathies]. | 1-gen-1984 | Federico, Antonio | - | |
| [Cerebrotendinous xanthomatosis. A case report]. | 1-gen-1996 | Sabadini, L; Gonnelli, L; Anichini, C; Funtò, I; Marcolongo, R; Dotti, Mg; Federico, Antonio | - | |
| [Complications and safety in the use of hyperbaric subarachnoid anesthesia in aged patients]. | 1-gen-1982 | Federico, Antonio; Ciccolo, F. | - | |
| [Italian neurology: past, present and future.] | 1-gen-2011 | Federico, Antonio | - | |
| [Multiple sclerosis. Etiopathogenetic review]. | 1-gen-1975 | Federico, Antonio | - | |
| [Rubinstein-Taybi syndrome with multiple keloids]. | 1-gen-1986 | Sammartino, A; Cerbella, R; Lembo, G; Federico, Antonio; Loffredo, L. | - | |
| A case of bilateral facial palsy with detection of herpes simplex virus type 1 DNA in the cerebrospinal fluid and serum anti-gm1 antibodies. | 1-gen-2009 | Rosini, Francesca; Pretegiani, Elena; D., Donati; D., Moschettini; Rubegni, Anna; Rufa, Alessandra; Annunziata, Pasquale; Federico, Antonio | - | |
| A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia. | 1-gen-2014 | Rubegni, A; Cardaioli, Elena; Chini, Elena; DA POZZO, Paola; Battisti, Carla; Malandrini, Alessandro; Federico, Antonio | - | |
| A CASE OF CEREBROTENDINOUS XANTHOMATOSIS PRESENTING WITH PARKINSONISM IN THE SEVENTH DECADE | 1-gen-2010 | Mignarri, Andrea; M., Falcini; Gallus, GIAN NICOLA; Giorgio, Antonio; Rufa, Alessandra; Ginanneschi, Federica; Federico, Antonio; Dotti, Maria | - | |
| A case of dystonia with onset during pregnancy. | 1-gen-2007 | Buccoliero, R; Palmeri, Silvia; Malandrini, Alessandro; Dotti, Maria; Federico, Antonio | - | |
| A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778. | 1-gen-1998 | Dotti, Maria; Plewnia, K; Cardaioli, Elena; Manneschi, L; Rufa, Alessandra; Alemà, G; Federico, Antonio | - | |
| A case of ovarioleukodystrophy without elF2B mutations. | 1-gen-2008 | Gaudiano, C; DI PERRI, C; Scali, O; Rufa, Alessandra; Battisti, Carla; DE STEFANO, Nicola; Federico, Antonio | - | |
| A case report of transient posterior internuclear ophthalmoplegia (PINO) associated with encephalitis of ponto-mesencephalic junction | 1-gen-2007 | Buccoliero, R; Rufa, Alessandra; A., Cerase; L., Monti; Malandrini, Alessandro; Federico, Antonio | - | |
| A new case of short-chain acyl-CoA dehydrogenase deficiency: clinical, biochemical, genetic and (1)H-NMR spectroscopic studies. | 1-gen-2007 | Battisti, C; Forte, F; Molinelli, MASSIMO CLAUDIO; Funghini, S; Pasquini, E; Tassini, M; Dotti, Maria; Federico, Antonio | - | |
| A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. | 1-gen-2005 | Sperduto, A; Dotti, Maria; DE STEFANO, Nicola; De Santis, M; Bianchi, Silvia; Rufa, Alessandra; Frantellizzi, P; Federico, Antonio | - | |
| 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 new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy | 1-gen-2012 | Cardaioli, Elena; Sicurelli, F; Carluccio, MARIA ALESSANDRA; Gallus, GIAN NICOLA; DA POZZO, Paola; Mondelli, M; Margollicci, Ma; Micheli, V; Federico, Antonio; Dotti, Maria | - | |
| A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids | 1-gen-2015 | DI DONATO, Ilaria; Stabile, Carmen; Bianchi, Silvia; Taglia, Ilaria; Mignarri, Andrea; Salvatore, Simona; Giorgio, Elisa; Brusco, Alfredo; Simone, Isabella; Dotti, Maria; Federico, Antonio | - |