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, 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 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, Ml; 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 visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL
2002-01-01 Rufa, Alessandra; Dotti, Maria; Bianchi, Silvia; DE STEFANO, Nicola; Federico, Antonio
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene
2016-01-01 DI GIOVANNI, Mario; Poggiani, A.; Bianchi, Silvia; Rosini, Francesca; Rufa, Alessandra; Federico, Antonio
Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism.
2014-01-01 Rosini, Francesca; Rufa, Alessandra; Monti, Lucia; Tirelli, Letizia; Federico, Antonio
| 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, 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 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, Ml; 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 visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL | 1-gen-2002 | Rufa, Alessandra; Dotti, Maria; Bianchi, Silvia; DE STEFANO, Nicola; Federico, Antonio | - | |
| Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene | 1-gen-2016 | DI GIOVANNI, Mario; Poggiani, A.; Bianchi, Silvia; Rosini, Francesca; Rufa, Alessandra; Federico, Antonio | - | |
| Adult-onset phenylketonuria revealed by acute reversible dementia, prosopagnosia and parkinsonism. | 1-gen-2014 | Rosini, Francesca; Rufa, Alessandra; Monti, Lucia; Tirelli, Letizia; Federico, Antonio | - |