Kolexia
Cuisset Jean-Marie
Pédiatrie
Hôpital Roger Salengro
Lille, France
145 Activités
19 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Myopathie de Duchenne Dystrophies musculaires Amyotrophie spinale Atrophie Amyotrophie Amyotrophies spinales infantiles Maladies musculaires Maladies neuromusculaires Myopathies congénitales structurales

Industries

AveXis
3 collaboration(s)
Dernière en 2019
Biogen
2 collaboration(s)
Dernière en 2019
INC RESEARCH, LLC
1 collaboration(s)
Dernière en 2019
Nutricia
1 collaboration(s)
Dernière en 2019

Dernières activités

OPALE: Observatoire Des Patients Atteints de Laminopathies et Emerinopathies (Observatory for PAtients With Laminopathies and Emerinopathies)
Essai Clinique (Hôpital Pitie Salpetriere)   13 décembre 2023
Confirmatory validation of the french version of the Duchenne Muscular Dystrophy module of the pediatric quality of life inventory (PedsQL 3.0DMDfv).
BMC pediatrics   15 novembre 2023
New insights into -related Joubert syndrome.
Journal of medical genetics   01 novembre 2022
Skeletal Ryanodine Receptors Are Involved in Impaired Myogenic Differentiation in Duchenne Muscular Dystrophy Patients.
International journal of molecular sciences   30 novembre 2021
COLLAGEN RELATED MUSCLE DISEASES: EP.59 Genetic etiology of retractile myopathies in a cohort of 80 children under 11 years following NGS analysis
Neuromuscular disorders : NMD   01 octobre 2021
Variable Presentation of Leber Hereditary Optic Neuropathy in Children of a Family Harboring a Rare m.13051G>A mtDNA Mutation.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society   22 septembre 2021
Amyotrophie spinale infantile
HAS Publications   25 mars 2021
The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMD.
Biomedicines   20 février 2021
Human pluripotent stem cells and artificial muscles for disease modelling of muscular dystrophies and therapy development
British Paediatric Neurology Association, Abstracts of the Annual Meeting, 6–8 January 2021, Virtual   30 décembre 2020
LATE BREAKING NEWS E-POSTER PRESENTATION: LBP 14 High-fidelity modelling of skeletal muscle laminopathies using LMNA-mutant human iPS cells and bioengineered muscles for mutation-specific therapy development
Neuromuscular disorders : NMD   01 octobre 2020