Kolexia
Meininger Vincent
Neurologie
Hôpital Pitie Salpetriere
Paris, France
137 Activités
135 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Sclérose latérale amyotrophique Sclérose Maladies du motoneurone Démence frontotemporale Prédisposition génétique à une maladie Dégénérescence lobaire frontotemporale Démence Atrophie Insuffisance respiratoire

Industries

Adliva
1 collaboration(s)
Dernière en 2019
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Dernières activités

Richard Leigh - Top podcast episodes - Listen Notes
Listen Notes Podcast   20 décembre 2023
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
Nature genetics   08 mars 2023
The p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with Mutations.
Biomedicines   24 février 2023
PULSE: Study of Predictive Factors of Progression of Motor Neurone Disease Prognosis and Endophenotype Biomarkers French Database Set up
Essai Clinique (CHU Lille)   04 novembre 2022
Comparison between PFN1 and SOD1 mutations in amyotrophic lateral sclerosis.
European journal of neurology   18 octobre 2022
The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis.
International journal of molecular sciences   19 mai 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles.
Journal of cachexia, sarcopenia and muscle   22 février 2022
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
Nature genetics   06 décembre 2021
Neurofilament light and heterogeneity of disease progression in amyotrophic lateral sclerosis: development and validation of a prediction model to improve interventional trials.
Translational neurodegeneration   26 août 2021
Impact of a frequent nearsplice variant in amyotrophic lateral sclerosis: optimising genetic screening for gene therapy opportunities.
Journal of neurology, neurosurgery, and psychiatry   30 mars 2021