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The capacity to consent to treatment in amyotrophic lateral sclerosis: a preliminary report

Journal of neurology, 2021, Vol.268 (1), p.219-226

2021

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Complete Locked-in and Locked-in Patients: Command Following Assessment and Communication with Vibro-Tactile P300 and Motor Imagery Brain-Computer Interface Tools

Frontiers in neuroscience, 2017-05, Vol.11, p.251-251

2017

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Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: Effect on survival

Journal of the neurological sciences, 2011-05, Vol.304 (1), p.44-48

2011

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Reaching and Grasping a Glass of Water by Locked-In ALS Patients through a BCI-Controlled Humanoid Robot

Frontiers in human neuroscience, 2017-03, Vol.11, p.68-68

2017

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A novel compound heterozygous mutation in GALC associated with adult-onset Krabbe disease: case report and literature review

Neurogenetics, 2022-04, Vol.23 (2), p.157-165

2022

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Factors affecting the diagnostic delay in amyotrophic lateral sclerosis

Clinical neurology and neurosurgery, 2012-07, Vol.114 (6), p.550-554

2012

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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

BMC neurology, 2023-06, Vol.23 (1), p.222-222, Article 222

2023

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A Human-Humanoid Interaction Through the Use of BCI for Locked-In ALS Patients Using Neuro-Biological Feedback Fusion

IEEE transactions on neural systems and rehabilitation engineering, 2018-02, Vol.26 (2), p.487-497

2018

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Editorial: Breakthrough BCI Applications in Medicine

Frontiers in neuroscience, 2020-12, Vol.14, p.598247-598247

2020

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How brain-computer interface technology may improve the diagnosis of the disorders of consciousness: A comparative study

Frontiers in neuroscience, 2022-08, Vol.16, p.959339-959339

2022

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Assessing Command-Following and Communication With Vibro-Tactile P300 Brain-Computer Interface Tools in Patients With Unresponsive Wakefulness Syndrome

Frontiers in neuroscience, 2018-06, Vol.12, p.423-423

2018

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Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis

Neurology, 2012-12, Vol.79 (24), p.2315

2012

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Effects of a Vibro-Tactile P300 Based Brain-Computer Interface on the Coma Recovery Scale-Revised in Patients With Disorders of Consciousness

Frontiers in neuroscience, 2020-04, Vol.14, p.294-294

2020

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Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

Human genomics, 2019-04, Vol.13 (1), p.19-19, Article 19

2019

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Corrigendum: Performance Differences Using a Vibro-Tactile P300 BCI in LIS-Patients Diagnosed With Stroke and ALS

Frontiers in neuroscience, 2021-01, Vol.14, p.637905-637905

2021

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Performance Differences Using a Vibro-Tactile P300 BCI in LIS-Patients Diagnosed With Stroke and ALS

Frontiers in neuroscience, 2018-07, Vol.12, p.514-514

2018

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Determinants of quality of life in locked-in and complete locked-in ALS patients

Journal of the neurological sciences, 2023-12, Vol.455, p.121085, Article 121085

2023

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FUS mutations in sporadic amyotrophic lateral sclerosis

Neurobiology of aging, 2011-03, Vol.32 (3), p.550.e1-550.e4

2011

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Bilateral Iatrogenic Femoral Neuropathy

Journal of Clinical Neurology, 2015, 11(4), , pp.398-399

2015

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Prognostic Role of CSF β-amyloid 1-42/1-40 Ratio in Patients Affected by Amyotrophic Lateral Sclerosis

Brain sciences, 2021-02, Vol.11 (3), p.302

2021

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Long-Lasting Cranial Nerve III Palsy as a Presenting Feature of Chronic Inflammatory Demyelinating Polyneuropathy

Case Reports in Medicine, 2015-01, Vol.2015, p.769429-3

2015

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FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis

Neurobiology of aging, 2012-04, Vol.33 (4), p.837.e1-837.e5

2012

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Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family

Journal of personalized medicine, 2020-12, Vol.10 (4), p.262

2020

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The relationship between working activity and disease progression in amyotrophic lateral sclerosis

Journal of the neurological sciences, 2023-12, Vol.455, p.121710, Article 121710

2023

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The capacity to consent to treatment in amyotrophic lateral sclerosis: a preliminary report

Complete Locked-in and Locked-in Patients: Command Following Assessment and Communication with Vibro-Tactile P300 and Motor Imagery Brain-Computer Interface Tools

Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: Effect on survival

Reaching and Grasping a Glass of Water by Locked-In ALS Patients through a BCI-Controlled Humanoid Robot

A novel compound heterozygous mutation in GALC associated with adult-onset Krabbe disease: case report and literature review

Factors affecting the diagnostic delay in amyotrophic lateral sclerosis

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

A Human-Humanoid Interaction Through the Use of BCI for Locked-In ALS Patients Using Neuro-Biological Feedback Fusion

Editorial: Breakthrough BCI Applications in Medicine

How brain-computer interface technology may improve the diagnosis of the disorders of consciousness: A comparative study

Assessing Command-Following and Communication With Vibro-Tactile P300 Brain-Computer Interface Tools in Patients With Unresponsive Wakefulness Syndrome

Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis

Effects of a Vibro-Tactile P300 Based Brain-Computer Interface on the Coma Recovery Scale-Revised in Patients With Disorders of Consciousness

Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

Corrigendum: Performance Differences Using a Vibro-Tactile P300 BCI in LIS-Patients Diagnosed With Stroke and ALS

Performance Differences Using a Vibro-Tactile P300 BCI in LIS-Patients Diagnosed With Stroke and ALS

Determinants of quality of life in locked-in and complete locked-in ALS patients

FUS mutations in sporadic amyotrophic lateral sclerosis

Bilateral Iatrogenic Femoral Neuropathy

Prognostic Role of CSF β-amyloid 1-42/1-40 Ratio in Patients Affected by Amyotrophic Lateral Sclerosis

The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations

Long-Lasting Cranial Nerve III Palsy as a Presenting Feature of Chronic Inflammatory Demyelinating Polyneuropathy

FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis

Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family

The relationship between working activity and disease progression in amyotrophic lateral sclerosis

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