Kolexia
Vicart Savine
Neurologie
Hôpital Pitie Salpetriere
Paris, France
56 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Paralysie Myotonie Canalopathies Myotonie congénitale Troubles myotoniques Maladies musculaires Paralysie périodique hypokaliémique Syndrome d'Andersen Myalgie

Industries

AXELYS SANTE
13 collaboration(s)
Dernière en 2022
LUPIN ATLANTIS HOLDINGS SA
7 collaboration(s)
Dernière en 2023
SUN PHARMA FRANCE
2 collaboration(s)
Dernière en 2022
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{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

P387 Initiation and follow-up of mexiletine treatment in adult myotonic dystrophy patients: an expert opinion
Neuromuscular disorders : NMD   01 octobre 2023
P395 Recommendations of an expert group for cardiac assessment of non-dystrophic myotonic adult patients treated with mexiletine
Neuromuscular disorders : NMD   01 octobre 2023
RaDiCo-PP: Utility and Validation's Study of a Smartphone Application for Periodic Paralysis
Essai Clinique (Institut National de la Santé Et de la Recherche Médicale, France)   26 juillet 2023
Caveolinopathy: Clinical, histological, and muscle imaging features and follow-up in a multicenter retrospective cohort.
European journal of neurology   25 mai 2023
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle Channelopathies.
Pediatric neurology   19 mai 2023
Phenotypical variability and atypical presentations in a French cohort of Andersen-Tawil syndrome.
European journal of neurology   04 mai 2022
E-Health & Innovation to Overcome Barriers in Neuromuscular Diseases. Report from the 1st eNMD Congress: Nice, France, March 22-23, 2019.
Journal of neuromuscular diseases   20 décembre 2021
Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision Medicine.
Journal of neuromuscular diseases   15 novembre 2021
A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases.
Orphanet journal of rare diseases   26 octobre 2021
CHANNELOPATHIES AND RELATED DISORDERS: EP.221 Diagnostic delay and atypical phenotypes in a French cohort of Andersen-Tawil syndrome
Neuromuscular disorders : NMD   01 octobre 2021