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Combination of serum and CSF neurofilament-light and neuroinflammatory biomarkers to evaluate ALS

Scientific reports, 2021-01, Vol.11 (1), p.703-703, Article 703

2021

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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Brain (London, England : 1878), 2014-08, Vol.137 (Pt 8), p.2329-2345

2014

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Region‐specific impairment of the cervical spinal cord (SC) in amyotrophic lateral sclerosis: A preliminary study using SC templates and quantitative MRI (diffusion tensor imaging/inhomogeneous magnetization transfer)

NMR in biomedicine, 2017-12, Vol.30 (12), p.n/a

2017

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Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

American journal of human genetics, 2009-09, Vol.85 (3), p.338-353

2009

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Retrospective clinical and genetic analysis of COL6-RD patients with a long-term follow-up at a single French center

Frontiers in genetics, 2023-12, Vol.14, p.1242277-1242277

2023

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New strategy for improving the diagnostic sensitivity of repetitive nerve stimulation in myasthenia gravis

Muscle & nerve, 2017-04, Vol.55 (4), p.532-538

2017

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Structural Connectivity Alterations in Amyotrophic Lateral Sclerosis: A Graph Theory Based Imaging Study

Frontiers in neuroscience, 2019-10, Vol.13, p.1044-1044

2019

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Clinical features and follow‐up of four new cases of facial‐onset sensory and motor neuronopathy

Muscle & nerve, 2011-01, Vol.43 (1), p.136-140

2011

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N°293 – Electrophysiological features of the peripheral neuropathy in cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS)

Clinical neurophysiology, 2023-06, Vol.150, p.e164-e164

2023

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Modafinil for the treatment of hypersomnia associated with myotonic muscular dystrophy in adults: A multicenter, prospective, randomized, double-blind, placebo-controlled, 4-week trial

Clinical therapeutics, 2009-08, Vol.31 (8), p.1765-1773

2009

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Lewis-Sumner syndrome and multifocal motor neuropathy

Muscle & nerve, 2005-01, Vol.31 (1), p.88-94

2005

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Syndrome post-poliomyélitique et séquelles de poliomyélite antérieure aiguë : un nouveau programme national de diagnostic et de soins

Revue neurologique, 2024-04, Vol.180, p.S104-S104

2024

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Consensus d’experts sur les échelles et critères utilisés en pratique pour le diagnostic et le suivi de la sclérose latérale amyotrophique en France

Revue neurologique, 2023-04, Vol.179, p.S141-S141

2023

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Treatment continuity of amyotrophic lateral sclerosis with available riluzole formulations: state of the art and current challenges in a ‘real-world’ setting

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-07, p.1-7

2024

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Could the motor unit number index be an early prognostic biomarker for amyotrophic lateral sclerosis?

Clinical neurophysiology, 2024-07, Vol.163, p.47-55

2024

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The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

Brain (London, England : 1878), 2012-01, Vol.135 (1), p.23-34

2012

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Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

Lancet neurology, 2021-01, Vol.20 (1), p.49-59

2021

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Face to Face: deciphering facial involvement in inclusion body myositis

Journal of neurology, 2024, Vol.271 (1), p.410-418

2024

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Association between brain and upper cervical spinal cord atrophy assessed by MRI and disease aggressiveness in amyotrophic lateral sclerosis

Neuroradiology, 2023-09, Vol.65 (9), p.1395-1403

2023

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Neurofilament Light Chain Levels Interact with Neurodegenerative Patterns and Motor Neuron Dysfunction in Amyotrophic Lateral Sclerosis

American journal of neuroradiology : AJNR, 2024-04, Vol.45 (4), p.494

2024

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Monitoring des effets à court terme des immunoglobulines intraveineuses dans la PIDC : quels sont les biomarqueurs les plus pertinents ?

Revue neurologique, 2024-04, Vol.180, p.S119-S119

2024

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Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 sera

Journal of neurology, 2020-12, Vol.267 (12), p.3664-3672

2020

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Multidisciplinary rehabilitation is relevant in severe myasthenia gravis: An observation

Annals of physical and rehabilitation medicine, 2022-09, Vol.65 (5), p.101593-101593, Article 101593

2022

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Conservative iron chelation for neurodegenerative diseases such as Parkinson’s disease and amyotrophic lateral sclerosis

Journal of Neural Transmission, 2020-02, Vol.127 (2), p.189-203

2020

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Quantitative Brain Sodium MRI Depicts Corticospinal Impairment in Amyotrophic Lateral Sclerosis

Radiology, 2019-08, Vol.292 (2), p.422

2019

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Combination of serum and CSF neurofilament-light and neuroinflammatory biomarkers to evaluate ALS

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Region‐specific impairment of the cervical spinal cord (SC) in amyotrophic lateral sclerosis: A preliminary study using SC templates and quantitative MRI (diffusion tensor imaging/inhomogeneous magnetization transfer)

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

Retrospective clinical and genetic analysis of COL6-RD patients with a long-term follow-up at a single French center

New strategy for improving the diagnostic sensitivity of repetitive nerve stimulation in myasthenia gravis

Structural Connectivity Alterations in Amyotrophic Lateral Sclerosis: A Graph Theory Based Imaging Study

Clinical features and follow‐up of four new cases of facial‐onset sensory and motor neuronopathy

N°293 – Electrophysiological features of the peripheral neuropathy in cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS)

Modafinil for the treatment of hypersomnia associated with myotonic muscular dystrophy in adults: A multicenter, prospective, randomized, double-blind, placebo-controlled, 4-week trial

Lewis-Sumner syndrome and multifocal motor neuropathy

Syndrome post-poliomyélitique et séquelles de poliomyélite antérieure aiguë : un nouveau programme national de diagnostic et de soins

Consensus d’experts sur les échelles et critères utilisés en pratique pour le diagnostic et le suivi de la sclérose latérale amyotrophique en France

Treatment continuity of amyotrophic lateral sclerosis with available riluzole formulations: state of the art and current challenges in a ‘real-world’ setting

Could the motor unit number index be an early prognostic biomarker for amyotrophic lateral sclerosis?

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

Face to Face: deciphering facial involvement in inclusion body myositis

Association between brain and upper cervical spinal cord atrophy assessed by MRI and disease aggressiveness in amyotrophic lateral sclerosis

Neurofilament Light Chain Levels Interact with Neurodegenerative Patterns and Motor Neuron Dysfunction in Amyotrophic Lateral Sclerosis

Monitoring des effets à court terme des immunoglobulines intraveineuses dans la PIDC : quels sont les biomarqueurs les plus pertinents ?

Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 sera

Multidisciplinary rehabilitation is relevant in severe myasthenia gravis: An observation

Conservative iron chelation for neurodegenerative diseases such as Parkinson’s disease and amyotrophic lateral sclerosis

Quantitative Brain Sodium MRI Depicts Corticospinal Impairment in Amyotrophic Lateral Sclerosis

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