Search Results - "Melzi, Lisa"

The effects of occipital and parietal tDCS on chronic visual field defects after brain injury by Diana, Lorenzo, Casati, Carlotta, Melzi, Lisa, Bianchi Marzoli, Stefania, Bolognini, Nadia

“…Homonymous visual field defects (HVFDs) following acquired brain lesions affect independent living by hampering several activities of everyday life. Available…”
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Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic Variants by Peverelli, Lorenzo, Catania, Alessia, Marchet, Silvia, Ciasca, Paola, Cammarata, Gabriella, Melzi, Lisa, Bellino, Antonella, Fancellu, Roberto, Lamantea, Eleonora, Capristo, Mariantonietta, Caporali, Leonardo, La Morgia, Chiara, Carelli, Valerio, Ghezzi, Daniele, Bianchi Marzoli, Stefania, Lamperti, Costanza

“…Leber's hereditary optic neuropathy (LHON) is due to missense point mutations affecting mitochondrial DNA (mtDNA); 90% of cases harbor the m.3460G>A,…”
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Explicit and Implicit Components of the Emotional Processing in Non-organic Vision Loss: Behavioral Evidence About the Role of Fear in Functional Blindness by Scarpina, Federica, Melzi, Lisa, Castelnuovo, Gianluca, Mauro, Alessandro, Marzoli, Stefania B, Molinari, Enrico

“…Non-organic vision loss (NOVL), a functional partial or global vision loss, might be considered a manifestation of conversion disorder. The few previous…”
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Evidence for retrochiasmatic tissue loss in Leber's hereditary optic neuropathy by Barcella, Valeria, Rocca, Maria A., Bianchi-Marzoli, Stefania, Milesi, Jacopo, Melzi, Lisa, Falini, Andrea, Pierro, Luisa, Filippi, Massimo

“…Patients with Leber's hereditary optic neuropathy (LHON) have loss of central vision with severe damage of small‐caliber fibers of the papillomacular bundle…”
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Repetition-priming effect: a cognitive task for the definition of a clinical assessment by Pagani, Silvia, Balconi, Michela, Sozzi, Matteo, Bianchi-Marzoli, Stefania, Melzi, Lisa, Corbo, Massimo

“…This research aims to study how semantic priming words can influence behavioral measures (RTs, accuracy), to develop an experimental paradigm to differentiate…”
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Quantification of retinal ganglion cell loss in patients with homonymous visual field defect due to stroke by Bianchi Marzoli, Stefania, Melzi, Lisa, Ciasca, Paola, Raggi, Alberto, Bersano, Anna, Casati, Carlotta, Bolognini, Nadia

“…Background To quantify the degree of ganglion cell degeneration through spectral domain optical coherence tomography (SD-OCT) in adult patients with…”
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ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy by Caporali, Leonardo, Magri, Stefania, Legati, Andrea, Del Dotto, Valentina, Tagliavini, Francesca, Balistreri, Francesca, Nasca, Alessia, La Morgia, Chiara, Carbonelli, Michele, Valentino, Maria L., Lamantea, Eleonora, Baratta, Silvia, Schöls, Ludger, Schüle, Rebecca, Barboni, Piero, Cascavilla, Maria L., Maresca, Alessandra, Capristo, Mariantonietta, Ardissone, Anna, Pareyson, Davide, Cammarata, Gabriella, Melzi, Lisa, Zeviani, Massimo, Peverelli, Lorenzo, Lamperti, Costanza, Marzoli, Stefania B., Fang, Mingyan, Synofzik, Matthis, Ghezzi, Daniele, Carelli, Valerio, Taroni, Franco

“…Objective Dominant optic atrophy (DOA) is the most common inherited optic neuropathy, with a prevalence of 1:12,000 to 1:25,000. OPA1 mutations are found in…”
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The Pre-Lumbar puncture Intracranial Hypertension Scale (PLIHS): A practical scale to identify subjects with normal cerebrospinal fluid pressure in the management of idiopathic intracranial hypertension by Raggi, Alberto, Bianchi Marzoli, Stefania, Ciasca, Paola, Cammarata, Gabriella, Melzi, Lisa, Chiapparini, Luisa, Erbetta, Alessandra, Ciceri, Elisa, Faragò, Giuseppe, Gioppo, Andrea, Usai, Susanna, D'Amico, Domenico

“…Idiopathic Intracranial Hypertension (IIH) diagnosis requires lumbar puncture to measure cerebrospinal fluid (CSF) pressure. The Pre-Lumbar puncture…”
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Optical coherence tomography in adult adrenoleukodystrophy: a cross-sectional and longitudinal study by Bianchi-Marzoli, Stefania, Fenu, Silvia, Melzi, Lisa, Benzoni, Chiara, Antonazzo, Filippo, Tomas Roldan, Eugenia, Farina, Laura, Tremolada, Gemma, Mauro, Elena, Pensato, Viviana, Gellera, Cinzia, Pareyson, Davide, Salsano, Ettore

“…Background Adrenoleukodystrophy (ALD) encompasses different neurological phenotypes, ranging from the most severe cerebral forms (C-ALD) to the less severe…”
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Abnormalities of the oculomotor function in type 1 diabetes and diabetic neuropathy by D’Addio, Francesca, Pastore, Ida, Loretelli, Cristian, Valderrama-Vasquez, Alessandro, Usuelli, Vera, Assi, Emma, Mameli, Chiara, Macedoni, Maddalena, Maestroni, Anna, Rossi, Antonio, Lunati, Maria Elena, Morpurgo, Paola Silvia, Gandolfi, Alessandra, Montefusco, Laura, Bolla, Andrea Mario, Ben Nasr, Moufida, Di Maggio, Stefania, Melzi, Lisa, Staurenghi, Giovanni, Secchi, Antonio, Bianchi Marzoli, Stefania, Zuccotti, Gianvincenzo, Fiorina, Paolo

“…Aims Abnormalities in the oculomotor system may represent an early sign of diabetic neuropathy and are currently poorly studied. We designed an…”
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Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy by Sagnelli, Anna, Piscosquito, Giuseppe, Di Bella, Daniela, Fadda, Laura, Melzi, Lisa, Morico, Antonio, Ciano, Claudia, Taroni, Franco, Facchetti, Dante, Salsano, Ettore, Pareyson, Davide

“…We report the first Italian family affected by hereditary gelsolin amyloidosis (HGA), a rare autosomal dominant disease characterized by adult‐onset slowly…”
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Which Differences in Priming Effect Between Neglect and Hemianopia? A Case Description of a Bilateral Brain-Lesioned Patient by Sozzi, Matteo, Bianchi Marzoli, Stefania, Melzi, Lisa, Corbo, Massimo, Venturella, Irene, Balconi, Michela

“…It is widely known that visuospatial neglect and hemianopia maybe superimposed. We considered the differences in implicit information processing which is…”
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Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy by Sagnelli, Anna, Piscosquito, Giuseppe, Di Bella, Daniela, Fadda, Laura, Melzi, Lisa, Morico, Antonio, Ciano, Claudia, Taroni, Franco, Facchetti, Dante, Salsano, Ettore, Pareyson, Davide

“…We report the first Italian family affected by hereditary gelsolin amyloidosis (HGA), a rare autosomal dominant disease characterized by adult-onset slowly…”
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