Search Results - "Spataro, Rossella"
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1
The capacity to consent to treatment in amyotrophic lateral sclerosis: a preliminary report
Published in Journal of neurology (2021)“…Background Facing the relentless worsening of their condition, ALS patients are required to make decisions on treatments and end-of-life care. A cognitive…”
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2
Complete Locked-in and Locked-in Patients: Command Following Assessment and Communication with Vibro-Tactile P300 and Motor Imagery Brain-Computer Interface Tools
Published in Frontiers in neuroscience (05-05-2017)“…Many patients with locked-in syndrome (LIS) or complete locked-in syndrome (CLIS) also need brain-computer interface (BCI) platforms that do not rely on visual…”
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3
Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: Effect on survival
Published in Journal of the neurological sciences (15-05-2011)“…Abstract Background Percutaneous endoscopic gastrostomy (PEG) is offered to amyotrophic lateral sclerosis (ALS) patients with severe dysphagia. Immediate…”
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4
Reaching and Grasping a Glass of Water by Locked-In ALS Patients through a BCI-Controlled Humanoid Robot
Published in Frontiers in human neuroscience (01-03-2017)“…Locked-in Amyotrophic Lateral Sclerosis (ALS) patients are fully dependent on caregivers for any daily need. At this stage, basic communication and…”
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5
A novel compound heterozygous mutation in GALC associated with adult-onset Krabbe disease: case report and literature review
Published in Neurogenetics (01-04-2022)“…Krabbe disease (KD) is a rare autosomal recessive lipid storage leukodystrophy. It is caused by deficient enzyme activity resulting from mutations of the…”
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6
Factors affecting the diagnostic delay in amyotrophic lateral sclerosis
Published in Clinical neurology and neurosurgery (01-07-2012)“…Abstract Background Although amyotrophic lateral sclerosis (ALS) is a relentlessly progressive disorder, early diagnosis allows a prompt start with the…”
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7
A Human-Humanoid Interaction Through the Use of BCI for Locked-In ALS Patients Using Neuro-Biological Feedback Fusion
Published in IEEE transactions on neural systems and rehabilitation engineering (01-02-2018)“…This paper illustrates a new architecture for a human-humanoid interaction based on EEG-brain computer interface (EEG-BCI) for patients affected by locked-in…”
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8
Role of the immune system in amyotrophic lateral sclerosis. Analysis of the natural killer cells and other circulating lymphocytes in a cohort of ALS patients
Published in BMC neurology (09-06-2023)“…Neuroinflammation might be involved in the degeneration and progression of Amyotrophic Lateral Sclerosis (ALS). Here, we studied the role of the circulating…”
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9
Editorial: Breakthrough BCI Applications in Medicine
Published in Frontiers in neuroscience (16-12-2020)“…BCIs for rehabilitation integrate BCIs with conventional methods and devices for rehabilitation like functional electrical stimulation (FES)-based…”
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10
How brain-computer interface technology may improve the diagnosis of the disorders of consciousness: A comparative study
Published in Frontiers in neuroscience (11-08-2022)“…Objective Clinical assessment of consciousness relies on behavioural assessments, which have several limitations. Hence, disorder of consciousness (DOC)…”
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11
Effects of a Vibro-Tactile P300 Based Brain-Computer Interface on the Coma Recovery Scale-Revised in Patients With Disorders of Consciousness
Published in Frontiers in neuroscience (09-04-2020)“…Persons diagnosed with disorders of consciousness (DOC) typically suffer from motor and cognitive disabilities. Recent research has shown that non-invasive…”
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12
Assessing Command-Following and Communication With Vibro-Tactile P300 Brain-Computer Interface Tools in Patients With Unresponsive Wakefulness Syndrome
Published in Frontiers in neuroscience (29-06-2018)“…Persons diagnosed with disorders of consciousness (DOC) typically suffer from motor disablities, and thus assessing their spared cognitive abilities can be…”
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13
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion
Published in Human genomics (16-04-2019)“…Amyotrophic lateral sclerosis [1] is a genetically heterogeneous neurodegenerative disorder, characterized by late-onset degeneration of motor neurons leading…”
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14
Corrigendum: Performance Differences Using a Vibro-Tactile P300 BCI in LIS-Patients Diagnosed With Stroke and ALS
Published in Frontiers in neuroscience (06-01-2021)“…[This corrects the article DOI: 10.3389/fnins.2018.00514.]…”
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15
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis
Published in Neurology (11-12-2012)“…Recent evidence suggests that intermediate-length polyglutamine (PolyQ) expansions in the ataxin-2 (ATXN-2) gene are a risk factor for amyotrophic lateral…”
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16
Performance Differences Using a Vibro-Tactile P300 BCI in LIS-Patients Diagnosed With Stroke and ALS
Published in Frontiers in neuroscience (31-07-2018)“…Patients with locked-in syndrome (LIS) are typically unable to move or communicate and can be misdiagnosed as patients with disorders of consciousness (DOC)…”
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17
FUS mutations in sporadic amyotrophic lateral sclerosis
Published in Neurobiology of aging (01-03-2011)“…Abstract Mutations in the FUS gene have recently been described as a cause of familial amyotrophic lateral sclerosis (ALS), but their role in the pathogenesis…”
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18
Bilateral Iatrogenic Femoral Neuropathy
Published in Journal of clinical neurology (Seoul, Korea) (01-10-2015)“…KCI Citation Count: 0…”
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19
Prognostic Role of CSF β-amyloid 1-42/1-40 Ratio in Patients Affected by Amyotrophic Lateral Sclerosis
Published in Brain sciences (27-02-2021)“…The involvement of β-amyloid (Aβ) in the pathogenesis of amyotrophic lateral sclerosis (ALS) has been widely discussed and its role in the disease is still a…”
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20
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations
Published in Biomedicines (24-02-2023)“…: Data from published studies about the effect of HFE polymorphisms on ALS risk, phenotype, and survival are still inconclusive. We aimed at evaluating whether…”
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