Nicolas Pageot
Montpellier, France
Last Updated: 09/26/2026
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Found 21 publications
Efficacy and safety of low-dose IL-2 as an add-on therapy to riluzole (MIROCALS): a phase 2b, double-blind, randomised, placebo-controlled trial.
Journal: Lancet (London, England)
Published: October 25, 2024
Reversible sub-acute motor neuron syndrome after mushroom intoxication masquerading as amyotrophic lateral sclerosis.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: November 26, 2021
Compound heterozygous P67S/D91A SOD1 mutations in an ALS family with apparently sporadic case.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: October 20, 2021
Increased worsening of amyotrophic lateral sclerosis patients during Covid-19-related lockdown in France.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: February 12, 2021
Amyotrophic lateral sclerosis transcriptomics reveals immunological effects of low-dose interleukin-2.
Journal: Brain communications
Published: January 05, 2021
Repeated 5-day cycles of low dose aldesleukin in amyotrophic lateral sclerosis (IMODALS): A phase 2a randomised, double-blind, placebo-controlled trial.
Journal: EBioMedicine
Published: March 31, 2020
Clinical Phenotype and Inheritance in Patients With C9ORF72 Hexanucleotide Repeat Expansion: Results From a Large French Cohort.
Journal: Frontiers in neuroscience
Published: February 12, 2020
Low 25OH Vitamin D Blood Levels Are Independently Associated With Higher Amyotrophic Lateral Sclerosis Severity Scores: Results From a Prospective Study.
Journal: Frontiers in neurology
Published: January 07, 2020
Rhythm disturbances as a potential early marker of Parkinson's disease in idiopathic REM sleep behavior disorder.
Journal: Annals of clinical and translational neurology
Published: November 22, 2019
High-dose pharmaceutical grade biotin (MD1003) in amyotrophic lateral sclerosis: A pilot study.
Journal: EClinicalMedicine
Published: June 30, 2019
Serum neurofilament light chain at time of diagnosis is an independent prognostic factor of survival in amyotrophic lateral sclerosis.
Journal: European journal of neurology
Published: May 23, 2019
Slowly progressive motor neuron disease with multi-system involvement related to p.E121G SOD1 mutation.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: November 29, 2016
Last Updated: 09/26/2026