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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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A patient-derived amyotrophic lateral sclerosis blood-brain barrier model for focused ultrasound-mediated anti-TDP-43 antibody delivery

Fluids and barriers of the CNS, 2024-08, Vol.21 (1), p.65-20, Article 65

2024

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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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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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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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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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Reversible radiculomyelitis after ChAdOx1 nCoV-19 vaccination

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

2022

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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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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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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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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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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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Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double‐blind, placebo‐controlled trial

European journal of neurology, 2023-01, Vol.30 (1), p.69-86

2023

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Investigating Repeat Expansions in NIPA1 , NOP56 , and NOTCH2NLC Genes: A Closer Look at Amyotrophic Lateral Sclerosis Patients from Southern Italy

Cells (Basel, Switzerland), 2024-04, Vol.13 (8), p.677

2024

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The Primitive Palmomental Reflex in Amyotrophic Lateral Sclerosis

European neurology, 2018-01, Vol.79 (3-4), p.187-191

2018

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Diabetic thoracic radiculopathy: a case of a young woman with clinical improvement following immunotherapy

BMJ case reports, 2020-12, Vol.13 (12), p.e236412

2020

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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

A patient-derived amyotrophic lateral sclerosis blood-brain barrier model for focused ultrasound-mediated anti-TDP-43 antibody delivery

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

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

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

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

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

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

Reversible radiculomyelitis after ChAdOx1 nCoV-19 vaccination

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

Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: Effect on survival

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

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

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

Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double‐blind, placebo‐controlled trial

Investigating Repeat Expansions in NIPA1 , NOP56 , and NOTCH2NLC Genes: A Closer Look at Amyotrophic Lateral Sclerosis Patients from Southern Italy

The Primitive Palmomental Reflex in Amyotrophic Lateral Sclerosis

Diabetic thoracic radiculopathy: a case of a young woman with clinical improvement following immunotherapy

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