Search Results - "Silani, Vincenzo"
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Neurofilament Light Chain as Biomarker for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
Published in Frontiers in neuroscience (21-06-2021)“…Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two related currently incurable neurodegenerative diseases. ALS is characterized by…”
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Clinical trials in amyotrophic lateral sclerosis: why so many negative trials and how can trials be improved?
Published in Lancet neurology (01-11-2014)“…Summary Amyotrophic lateral sclerosis (ALS) is one of the most rapidly progressive neurodegenerative diseases of unknown cause. Riluzole is the only drug that…”
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Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (03-04-2017)“…This article presents the revised consensus criteria for the diagnosis of frontotemporal dysfunction in amyotrophic lateral sclerosis (ALS) based on an…”
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Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis
Published in Journal of neurology, neurosurgery and psychiatry (01-02-2019)“…ObjectiveTo determine the diagnostic and prognostic performance of serum neurofilament light chain (NFL) in amyotrophic lateral sclerosis (ALS).MethodsThis…”
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Primary lateral sclerosis: consensus diagnostic criteria
Published in Journal of neurology, neurosurgery and psychiatry (01-04-2020)“…Primary lateral sclerosis (PLS) is a neurodegenerative disorder of the adult motor system. Characterised by a slowly progressive upper motor neuron syndrome,…”
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SUMOylation Regulates TDP-43 Splicing Activity and Nucleocytoplasmic Distribution
Published in Molecular neurobiology (01-11-2021)“…The nuclear RNA-binding protein TDP-43 forms abnormal cytoplasmic aggregates in the brains of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia…”
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TDP-43 is recruited to stress granules in conditions of oxidative insult
Published in Journal of neurochemistry (01-11-2009)“…Transactive response DNA-binding protein 43 (TDP-43) forms abnormal ubiquitinated and phosphorylated inclusions in brain tissues from patients with amyotrophic…”
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An Italian multicenter retrospective-prospective observational study on neurological manifestations of COVID-19 (NEUROCOVID)
Published in Neurological sciences (01-06-2020)“…Neurological manifestations of COVID-19 have been described in both single case reports and retrospective scanty case series. They may be linked to the…”
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Chronic stress induces formation of stress granules and pathological TDP-43 aggregates in human ALS fibroblasts and iPSC-motoneurons
Published in Neurobiology of disease (01-11-2020)“…Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are fatal neurodegenerative diseases characterized by the presence of neuropathological…”
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Multicenter evaluation of neurofilaments in early symptom onset amyotrophic lateral sclerosis
Published in Neurology (02-01-2018)“…OBJECTIVETo examine neurofilament (Nf) concentrations according to symptom onset and clinical diagnostic certainty categories of amyotrophic lateral sclerosis…”
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EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) - revised report of an EFNS task force
Published in European journal of neurology (01-03-2012)“…Background: The evidence base for the diagnosis and management of amyotrophic lateral sclerosis (ALS) is weak. Objectives: To provide evidence‐based or…”
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A susceptibility-weighted imaging qualitative score of the motor cortex may be a useful tool for distinguishing clinical phenotypes in amyotrophic lateral sclerosis
Published in European radiology (01-03-2021)“…Objectives To distinguish amyotrophic lateral sclerosis (ALS) and its subtypes from ALS mimics and healthy controls based on the assessment of iron-related…”
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Long-Lasting Cognitive Abnormalities after COVID-19
Published in Brain sciences (13-02-2021)“…Considering the mechanisms capable of causing brain alterations in COVID-19, we aimed to study the occurrence of cognitive abnormalities in the months…”
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The preferences of people with amyotrophic lateral sclerosis on riluzole treatment in Europe
Published in Scientific reports (15-12-2023)“…The Patient Preference Survey aims to understand unmet needs related to riluzole management in people with Amyotrophic Lateral Sclerosis (ALS) and to identify…”
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GRN−/− iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosis
Published in Neurobiology of disease (01-12-2022)“…Heterozygous mutations in the gene coding for progranulin (GRN) cause frontotemporal lobar degeneration (FTLD) while homozygous mutations are linked to…”
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Advance care planning and mental capacity in ALS: a current challenge for an unsolved matter
Published in Neurological sciences (01-10-2020)Get full text
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Unilateral freezing of gait or “magnetic feet phenomenon” caused by ischemic lesion involving fronto-striatal networks
Published in Neurological sciences (01-08-2021)Get full text
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Testing olfactory dysfunction in acute and recovered COVID-19 patients: a single center study in Italy
Published in Neurological sciences (01-06-2021)“…Background Olfactory dysfunction in coronavirus disease 2019 (COVID-19) is common during acute illness and appears to last longer than other symptoms. The aim…”
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Rising evidence for neurological involvement in COVID-19 pandemic
Published in Neurological sciences (01-06-2020)Get full text
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Duropathy as a rare motor neuron disease mimic: from bibrachial amyotrophy to infratentorial superficial siderosis
Published in BMC neurology (02-09-2024)“…Bibrachial amyotrophy associated with an extradural CSF collection and infratentorial superficial siderosis (SS) are rare conditions that may occasionally…”
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