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ALS-linked FUS mutations confer loss and gain of function in the nucleus by promoting excessive formation of dysfunctional paraspeckles

Acta neuropathologica communications, 2019-01, Vol.7 (1), p.7-7, Article 7

2019

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Diagnostic Role of Tau Proteins in Amyotrophic Lateral Sclerosis: A Systematic Review and Meta-Analysis

Acta neurologica Scandinavica, 2023-03, Vol.2023, p.1-10

2023

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CSF neurofilament proteins as diagnostic and prognostic biomarkers for amyotrophic lateral sclerosis

Journal of neurology, 2018-03, Vol.265 (3), p.510-521

2018

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The role of ethical attitudes in the mortality of patients with disorders of consciousness

European journal of neurology, 2022-11, Vol.29 (11), p.3473-3474

2022

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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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Randomized double-blind placebo-controlled trial of acetyl-L-carnitine for ALS

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2013-09, Vol.14 (5-6), p.397-405

2013

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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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A Deletion of the Nuclear Localization Signal Domain in the Fus Protein Induces Stable Post-stress Cytoplasmic Inclusions in SH-SY5Y Cells

Frontiers in neuroscience, 2021-12, Vol.15, p.759659-759659

2021

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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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Reversible radiculomyelitis after ChAdOx1 nCoV-19 vaccination

BMJ case reports, 2022-02, Vol.15 (2), p.e247472

2022

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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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Tau protein as a diagnostic and prognostic biomarker in amyotrophic lateral sclerosis

European journal of neurology, 2021-06, Vol.28 (6), p.1868-1875

2021

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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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Expression and developmental regulation of the cystine/glutamate exchanger (xc-) in the rat

Neurochemical research, 2007-06, Vol.32 (6), p.1081-1090

2007

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ALS monocyte-derived microglia-like cells reveal cytoplasmic TDP-43 accumulation, DNA damage, and cell-specific impairment of phagocytosis associated with disease progression

Journal of neuroinflammation, 2022-02, Vol.19 (1), p.58-58, Article 58

2022

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Deregulation of Plasma microRNA Expression in a TARDBP -ALS Family

Biomolecules (Basel, Switzerland), 2023-04, Vol.13 (4), p.706

2023

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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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Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.784-793

2012

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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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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

2018

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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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Early and rapidly progressing respiratory failure in a patient with amyotrophic lateral sclerosis: when FVC% is misleading

Neurological sciences, 2019-02, Vol.40 (2), p.421-422

2019

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Biomarkers Related to Synaptic Dysfunction to Discriminate Alzheimer's Disease from Other Neurological Disorders

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10831

2022

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ALS-linked FUS mutations confer loss and gain of function in the nucleus by promoting excessive formation of dysfunctional paraspeckles

Diagnostic Role of Tau Proteins in Amyotrophic Lateral Sclerosis: A Systematic Review and Meta-Analysis

CSF neurofilament proteins as diagnostic and prognostic biomarkers for amyotrophic lateral sclerosis

The role of ethical attitudes in the mortality of patients with disorders of consciousness

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

Randomized double-blind placebo-controlled trial of acetyl-L-carnitine for ALS

Protein misfolding, amyotrophic lateral sclerosis and guanabenz: protocol for a phase II RCT with futility design (ProMISe trial)

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

A Deletion of the Nuclear Localization Signal Domain in the Fus Protein Induces Stable Post-stress Cytoplasmic Inclusions in SH-SY5Y Cells

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

Reversible radiculomyelitis after ChAdOx1 nCoV-19 vaccination

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

Tau protein as a diagnostic and prognostic biomarker in amyotrophic lateral sclerosis

Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: Effect on survival

Expression and developmental regulation of the cystine/glutamate exchanger (xc-) in the rat

ALS monocyte-derived microglia-like cells reveal cytoplasmic TDP-43 accumulation, DNA damage, and cell-specific impairment of phagocytosis associated with disease progression

Deregulation of Plasma microRNA Expression in a TARDBP -ALS Family

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

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

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

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

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

Early and rapidly progressing respiratory failure in a patient with amyotrophic lateral sclerosis: when FVC% is misleading

Biomarkers Related to Synaptic Dysfunction to Discriminate Alzheimer's Disease from Other Neurological Disorders

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