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Machine Learning in Amyotrophic Lateral Sclerosis: Achievements, Pitfalls, and Future Directions

Frontiers in neuroscience, 2019-02, Vol.13, p.135-135

2019

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Exceptional euthanasia: a theoretical construct or medical necessity?

The Lancet (British edition), 2024-04, Vol.403 (10435), p.1443-1443

2024

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Time for optimism in amyotrophic lateral sclerosis

European journal of neurology, 2023-05, Vol.30 (5), p.1459-1464

2023

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Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging study

Annals of neurology, 2019-08, Vol.86 (2), p.158-167

2019

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Development and validation of a 1-year survival prognosis estimation model for Amyotrophic Lateral Sclerosis using manifold learning algorithm UMAP

Scientific reports, 2020-08, Vol.10 (1), p.13378-13378, Article 13378

2020

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Energy metabolism in amyotrophic lateral sclerosis

Lancet neurology, 2011, Vol.10 (1), p.75-82

2011

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The changing landscape of motor neuron disease imaging: the transition from descriptive studies to precision clinical tools

Current opinion in neurology, 2018-08, Vol.31 (4), p.431-438

2018

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Radiation-induced neuropathy in cancer survivors

Radiotherapy and oncology, 2012-12, Vol.105 (3), p.273-282

2012

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Split-hand and split-limb phenomena in amyotrophic lateral sclerosis: pathophysiology, electrophysiology and clinical manifestations

Journal of neurology, neurosurgery and psychiatry, 2021-10, Vol.92 (10), p.1126

2021

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A retrospective analysis of all‐cause and cause‐specific mortality rates in French male professional footballers

Scandinavian journal of medicine & science in sports, 2022-09, Vol.32 (9), p.1389-1399

2022

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Spinal Cord Imaging in Amyotrophic Lateral Sclerosis: Historical Concepts-Novel Techniques

Frontiers in neurology, 2019-04, Vol.10, p.350-350

2019

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Absence of hyperexcitability of spinal motoneurons in patients with amyotrophic lateral sclerosis

The Journal of physiology, 2019-11, Vol.597 (22), p.5445-5467

2019

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A pharmaco-metabolomics approach in a clinical trial of ALS: Identification of predictive markers of progression

PloS one, 2018-06, Vol.13 (6), p.e0198116-e0198116

2018

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Transient increase in recurrent inhibition in amyotrophic lateral sclerosis as a putative protection from neurodegeneration

Acta Physiologica, 2022-04, Vol.234 (4), p.e13758-n/a

2022

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Manifold learning for amyotrophic lateral sclerosis functional loss assessment: Development and validation of a prognosis model

Journal of neurology, 2021-03, Vol.268 (3), p.825-850

2021

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Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas

Journal of personalized medicine, 2022-09, Vol.12 (10), p.1601

2022

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Extrapyramidal deficits in ALS: a combined biomechanical and neuroimaging study

Journal of neurology, 2018-09, Vol.265 (9), p.2125-2136

2018

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Interaction of sex and onset site on the disease trajectory of amyotrophic lateral sclerosis

Journal of neurology, 2023-12, Vol.270 (12), p.5903-5912

2023

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Environmental risk factors for amyotrophic lateral sclerosis: a case-control study in Canada and France

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2022-10, Vol.23 (7-8), p.592-600

2022

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Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression

Brain (London, England : 1878), 2013-08, Vol.136 (Pt 8), p.2359-2368

2013

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The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendations

Orphanet journal of rare diseases, 2020-04, Vol.15 (1), p.90-90, Article 90

2020

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Theoretical discrimination index of postural instability in amyotrophic lateral sclerosis

Scientific reports, 2022-02, Vol.12 (1), p.2430-2430, Article 2430

2022

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Cerebellar degeneration in adult spinal muscular atrophy patients

Journal of neurology, 2020-09, Vol.267 (9), p.2625-2631

2020

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Development of new outcome measures for adult SMA type III and IV: a multimodal longitudinal study

Journal of neurology, 2021-05, Vol.268 (5), p.1792-1802

2021

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Multi-parametric spinal cord MRI as potential progression marker in amyotrophic lateral sclerosis

PloS one, 2014-04, Vol.9 (4), p.e95516-e95516

2014

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Machine Learning in Amyotrophic Lateral Sclerosis: Achievements, Pitfalls, and Future Directions

Exceptional euthanasia: a theoretical construct or medical necessity?

Time for optimism in amyotrophic lateral sclerosis

Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging study

Development and validation of a 1-year survival prognosis estimation model for Amyotrophic Lateral Sclerosis using manifold learning algorithm UMAP

Energy metabolism in amyotrophic lateral sclerosis

The changing landscape of motor neuron disease imaging: the transition from descriptive studies to precision clinical tools

Radiation-induced neuropathy in cancer survivors

Split-hand and split-limb phenomena in amyotrophic lateral sclerosis: pathophysiology, electrophysiology and clinical manifestations

A retrospective analysis of all‐cause and cause‐specific mortality rates in French male professional footballers

Spinal Cord Imaging in Amyotrophic Lateral Sclerosis: Historical Concepts-Novel Techniques

Absence of hyperexcitability of spinal motoneurons in patients with amyotrophic lateral sclerosis

A pharmaco-metabolomics approach in a clinical trial of ALS: Identification of predictive markers of progression

Transient increase in recurrent inhibition in amyotrophic lateral sclerosis as a putative protection from neurodegeneration

Manifold learning for amyotrophic lateral sclerosis functional loss assessment: Development and validation of a prognosis model

Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas

Extrapyramidal deficits in ALS: a combined biomechanical and neuroimaging study

Interaction of sex and onset site on the disease trajectory of amyotrophic lateral sclerosis

Environmental risk factors for amyotrophic lateral sclerosis: a case-control study in Canada and France

Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression

The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendations

Theoretical discrimination index of postural instability in amyotrophic lateral sclerosis

Cerebellar degeneration in adult spinal muscular atrophy patients

Development of new outcome measures for adult SMA type III and IV: a multimodal longitudinal study

Multi-parametric spinal cord MRI as potential progression marker in amyotrophic lateral sclerosis

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