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Lisa Melzi

Explore the profile of Lisa Melzi including associated specialties, affiliations and a list of published articles. Areas
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Articles 12
Citations 80
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Recent Articles
1.
Bolognini N, Diana L, Rossetti A, Melzi L, Basso G, Manzo V, et al.
J Neuroeng Rehabil . 2025 Feb; 22(1):34. PMID: 39994637
Background: Acquired homonymous visual field defects (HVFDs) result in significant disability, reducing quality of life. Spontaneous recovery occurs within the first months, then the likelihood of vision recovery decreases, making...
2.
Diana L, Casati C, Melzi L, Bianchi Marzoli S, Bolognini N
Eur J Neurol . 2024 Nov; 32(1):e16559. PMID: 39607286
Background And Purpose: Visual rehabilitation is necessary for improving the quality of life of patients with acquired homonymous visual field defects (HVFDs). By modulating brain excitability and plasticity, transcranial direct...
3.
Diana L, Casati C, Melzi L, Bianchi Marzoli S, Bolognini N
Front Neurol . 2024 Feb; 15:1340365. PMID: 38419713
Introduction: Homonymous visual field defects (HVFDs) following acquired brain lesions affect independent living by hampering several activities of everyday life. Available treatments are intensive and week- or month-long. Transcranial Direct...
4.
Bianchi Marzoli S, Melzi L, Ciasca P, Raggi A, Bersano A, Casati C, et al.
Neurol Sci . 2023 Mar; 44(8):2811-2819. PMID: 36905449
Background: To quantify the degree of ganglion cell degeneration through spectral domain optical coherence tomography (SD-OCT) in adult patients with post-stroke homonymous visual field defect. Methods: Fifty patients with acquired...
5.
DAddio F, Pastore I, Loretelli C, Valderrama-Vasquez A, Usuelli V, Assi E, et al.
Acta Diabetol . 2022 Jun; 59(9):1157-1167. PMID: 35729357
Aims: Abnormalities in the oculomotor system may represent an early sign of diabetic neuropathy and are currently poorly studied. We designed an eye-tracking-based test to evaluate oculomotor function in patients...
6.
Raggi A, Bianchi Marzoli S, Ciasca P, Cammarata G, Melzi L, Chiapparini L, et al.
J Neurol Sci . 2021 Aug; 429:118058. PMID: 34461550
Background: Idiopathic Intracranial Hypertension (IIH) diagnosis requires lumbar puncture to measure cerebrospinal fluid (CSF) pressure. The Pre-Lumbar puncture Intracranial Hypertension Scale (PLIHS) is aimed to detect cases that will show...
7.
Peverelli L, Catania A, Marchet S, Ciasca P, Cammarata G, Melzi L, et al.
Front Neurol . 2021 Jun; 12:657317. PMID: 34177762
Leber's hereditary optic neuropathy (LHON) is due to missense point mutations affecting mitochondrial DNA (mtDNA); 90% of cases harbor the m.3460G>A, m.11778G>A, and m.14484T>C primary mutations. Here, we report and...
8.
Bianchi-Marzoli S, Fenu S, Melzi L, Benzoni C, Antonazzo F, Tomas Roldan E, et al.
Neurol Sci . 2020 Jul; 42(1):235-241. PMID: 32632637
Background: Adrenoleukodystrophy (ALD) encompasses different neurological phenotypes, ranging from the most severe cerebral forms (C-ALD) to the less severe adrenomyeloneuropathy (AMN). As visual system can be varyingly involved, we aimed...
9.
Caporali L, Magri S, Legati A, Del Dotto V, Tagliavini F, Balistreri F, et al.
Ann Neurol . 2020 Mar; 88(1):18-32. PMID: 32219868
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 70% of DOA patients, with a...
10.
Scarpina F, Melzi L, Castelnuovo G, Mauro A, Marzoli S, Molinari E
Front Psychol . 2018 Apr; 9:494. PMID: 29692751
Non-organic vision loss (NOVL), a functional partial or global vision loss, might be considered a manifestation of conversion disorder. The few previous studies focused on investigating the relationship between cerebral...