Kolexia
Vial Christophe
Neurologie
Hôpital Pierre Wertheimer
Bron, France
97 Activités
0 Followers

Scientifique
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{{person.topmesh1.name}} Neuropathies périphériques Polyneuropathies Sclérose latérale amyotrophique Sclérose Dystrophies musculaires Dystonie Myasthénie Maladies du motoneurone Dystrophie musculaire facio-scapulo-humérale

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Ipsen
6 collaboration(s)
Dernière en 2021
Allergan
1 collaboration(s)
Dernière en 2020
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Dernières activités

Clinical, Genetic and Epigenetic Characterization of Patients With FSHD Type 1 and FSHD Type 2
Essai Clinique (CHU Nice)   10 novembre 2023
Myasthenia gravis treatment in the elderly presents with a significant iatrogenic risk: a multicentric retrospective study.
Journal of neurology   17 août 2023
Food aeration: Effect of the surface-active agent type on bubble deformation and break-up in a viscous Newtonian fluid: From single bubble to process-scale.
Food research international (Ottawa, Ont.)   13 janvier 2023
Immune-Mediated Rippling Muscle Disease Associated With Thymoma and Anti-MURC/Cavin-4 Autoantibodies.
Neurology(R) neuroimmunology & neuroinflammation   15 décembre 2022
Miastenia e sindromi miasteniche
EMC - Neurologia   01 août 2020
The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendations.
Orphanet journal of rare diseases   10 avril 2020
Electrophysiological Characterization of C9ORF72-Associated Amyotrophic Lateral Sclerosis: A Retrospective Study.
European neurology   04 février 2020
Ulnar neuropathy at the elbow: Reappraisal of the wrist-upper arm latency difference between ulnar and median nerves.
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology   06 décembre 2019
Prospective study of the additional benefit of plexus magnetic resonance imaging in the diagnosis of chronic inflammatory demyelinating polyneuropathy.
European journal of neurology   12 août 2019
Dilated cardiomyopathy and limb-girdle muscular dystrophy-dystroglycanopathy due to novel pathogenic variants in the DPM3 gene.
Neuromuscular disorders : NMD   09 mai 2019