RUFA, ALESSANDRA

RUFA, ALESSANDRA  

Dipartimento di Scienze Mediche, Chirurgiche e Neuroscienze  

Mostra records
Risultati 1 - 20 di 204 (tempo di esecuzione: 0.0 secondi).
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 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, A.; Dotti, M. T.; Bianchi, S.; De Stefano, N.; Federico, A. -
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 -