RUFA, ALESSANDRA
RUFA, ALESSANDRA
Dipartimento di Scienze Mediche, Chirurgiche e Neuroscienze
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 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 ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778
1998-01-01 Dotti, M. T.; Plewnia, K.; Cardaioli, E.; Manneschi, L.; Rufa, A.; Alemà, G.; Federico, A.
A case of ovarioleukodystrophy without elF2B mutations
2008-01-01 Gaudiano, C.; Di PerriI, C.; Scali, O.; Rufa, Alessandra; Battisti, Carla; De Stefano, Nicola; Federico, Antonio
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis
2022-01-01 Lopergolo, D.; Berti, G.; Mari, F.; Bertini, E.; Rufa, A.; Battisti, C.; Sicurelli, F.; Renieri, A.; Federico, A.; Sandhoff, K.; Malandrini, A.
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 cross-recurrence analysis of the pupil size fluctuations in steady scotopic conditions
2019-01-01 Piu, P.; Serchi, V.; Rosini, F.; Rufa, A.
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 novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy.
2006-01-01 Cardaioli, E; Gallus, GIAN NICOLA; DA POZZO, P; Rufa, Alessandra; Franceschini, Rossella; Motolese, Eduardo; Caporossi, A; Dotti, Maria; Federico, Antonio
A novel OPA1 mutation resulting in atypical dominant optic atrophy with NTG “Like” phenotype.
2006-01-01 Rufa, Alessandra; Cardaioli, E; Gallus, GIAN NICOLA; Da Pozzo, P; Frezzotti, P; Dotti, Maria; Renieri, Alessandra; Longo, I; Federico, Antonio
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features
2010-01-01 Malfatti, E.; Cardaioli, E.; Battisti, C.; Da Pozzo, P.; Malandrini, Alessandro; Rufa, Alessandra; Rocchi, Raffaele; Federico, Antonio
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case
1997-01-01 Plewnia, K; Dotti, Maria; Malandrini, Alessandro; Manneschi, L; Battisti, Carla; DE STEFANO, Nicola; Rufa, Alessandra; Motolese, Eduardo; Federico, Antonio
A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making
2014-01-01 Piu, Pietro; Fargnoli, Francesco; Innocenti, Alessandro; Rufa, Alessandra
A unified computational framework for visual attention dynamics
2019-01-01 Zanca, D.; Gori, M.; Rufa, A.
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases
2018-01-01 Taglia, I.; Di Donato, I.; Bianchi, S.; Cerase, A.; Monti, L.; Marconi, R.; Orrico, A.; Rufa, A.; Federico, A.; Dotti, M. T.
Action and perception are temporally coupled by a common mechanism that leads to a timing misperception
2015-01-01 Pretegiani, Elena; Astefanoaei, Corina; Daye, Pierre M; Fitzgibbon, Edmond J; Creanga, Dorina Emilia; Rufa, Alessandra; Optican, Lance M.
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
2004-01-01 Rufa, Alessandra; De Stefano, Nicola; Dotti, Maria; Bianchi, Silvia; Sicurelli, F.; Stromillo, M. l.; Daniello, B.; Federico, Antonio
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
2008-01-01 Rufa, Alessandra; Cerase, A.; Monti, L.; Battisti, C.; Forte, F.; Federico, Antonio; Dotti, Maria
Acute vision disorders
2020-01-01 Bergamaschi, R.; Colnaghi, S.; Giometto, B.; Rufa, A.; Sacco, S.; Vita, G.
Acute visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL
2002-01-01 Rufa, A.; Dotti, M. T.; Bianchi, S.; De Stefano, N.; Federico, A.
| Titolo | Data di pubblicazione | Autore(i) | File | Abstract |
|---|---|---|---|---|
| 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 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 ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778 | 1-gen-1998 | Dotti, M. T.; Plewnia, K.; Cardaioli, E.; Manneschi, L.; Rufa, A.; Alemà, G.; Federico, A. | - | |
| A case of ovarioleukodystrophy without elF2B mutations | 1-gen-2008 | Gaudiano, C.; Di PerriI, C.; Scali, O.; Rufa, Alessandra; Battisti, Carla; De Stefano, Nicola; Federico, Antonio | - | |
| A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis | 1-gen-2022 | Lopergolo, D.; Berti, G.; Mari, F.; Bertini, E.; Rufa, A.; Battisti, C.; Sicurelli, F.; Renieri, A.; Federico, A.; Sandhoff, K.; Malandrini, A. | - | |
| 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 cross-recurrence analysis of the pupil size fluctuations in steady scotopic conditions | 1-gen-2019 | Piu, P.; Serchi, V.; Rosini, F.; Rufa, A. | - | |
| 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 novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. | 1-gen-2006 | Cardaioli, E; Gallus, GIAN NICOLA; DA POZZO, P; Rufa, Alessandra; Franceschini, Rossella; Motolese, Eduardo; Caporossi, A; Dotti, Maria; Federico, Antonio | - | |
| A novel OPA1 mutation resulting in atypical dominant optic atrophy with NTG “Like” phenotype. | 1-gen-2006 | Rufa, Alessandra; Cardaioli, E; Gallus, GIAN NICOLA; Da Pozzo, P; Frezzotti, P; Dotti, Maria; Renieri, Alessandra; Longo, I; Federico, Antonio | - | |
| A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features | 1-gen-2010 | Malfatti, E.; Cardaioli, E.; Battisti, C.; Da Pozzo, P.; Malandrini, Alessandro; Rufa, Alessandra; Rocchi, Raffaele; Federico, Antonio | - | |
| A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case | 1-gen-1997 | Plewnia, K; Dotti, Maria; Malandrini, Alessandro; Manneschi, L; Battisti, Carla; DE STEFANO, Nicola; Rufa, Alessandra; Motolese, Eduardo; Federico, Antonio | - | |
| A two-layered diffusion model traces the dynamics of information processing in the valuation-and-choice circuit of decision making | 1-gen-2014 | Piu, Pietro; Fargnoli, Francesco; Innocenti, Alessandro; Rufa, Alessandra | - | |
| A unified computational framework for visual attention dynamics | 1-gen-2019 | Zanca, D.; Gori, M.; Rufa, A. | - | |
| AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases | 1-gen-2018 | Taglia, I.; Di Donato, I.; Bianchi, S.; Cerase, A.; Monti, L.; Marconi, R.; Orrico, A.; Rufa, A.; Federico, A.; Dotti, M. T. | - | |
| Action and perception are temporally coupled by a common mechanism that leads to a timing misperception | 1-gen-2015 | Pretegiani, Elena; Astefanoaei, Corina; Daye, Pierre M; Fitzgibbon, Edmond J; Creanga, Dorina Emilia; Rufa, Alessandra; Optican, Lance M. | - | |
| Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy | 1-gen-2004 | Rufa, Alessandra; De Stefano, Nicola; Dotti, Maria; Bianchi, Silvia; Sicurelli, F.; Stromillo, M. l.; Daniello, B.; Federico, Antonio | - | |
| Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL) | 1-gen-2008 | Rufa, Alessandra; Cerase, A.; Monti, L.; Battisti, C.; Forte, F.; Federico, Antonio; Dotti, Maria | - | |
| Acute vision disorders | 1-gen-2020 | Bergamaschi, R.; Colnaghi, S.; Giometto, B.; Rufa, A.; Sacco, S.; Vita, G. | - | |
| Acute visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL | 1-gen-2002 | Rufa, A.; Dotti, M. T.; Bianchi, S.; De Stefano, N.; Federico, A. | - |