Kolexia
Carlier Robert
Radio-diagnostic
Hôpital Raymond-Poincaré
Garches, France
272 Activités
222 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Maladies musculaires Dystrophies musculaires COVID-19 Scoliose Glycogénose de type II Myopathies congénitales structurales Glycogénose Myosite Infections à VIH

Industries

Biogen
7 collaboration(s)
Dernière en 2023
Boston Scientific
2 collaboration(s)
Dernière en 2021
Sanofi
1 collaboration(s)
Dernière en 2023
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{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

Correction to: Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP‑mediated disease reveals characteristic features useful for diagnosis.
Journal of neurology   13 février 2024
A Caribbean case of phosphoglycerate mutase deficiency: Relevance of forearm exercise test and electroneuromyography with long exercise test in the diagnosis strategy of rare muscle glycogenosis
Medical Reports   01 février 2024
The Ala1186Val Variant Linked to Cytoplasmic Body Myopathy and Cardiomyopathy Causes Protein Instability.
Biomedicines   30 janvier 2024
Infectious sacroiliitis: MRI- and CT-based assessment of disease extent, complications, and anatomic correlation.
Skeletal radiology   18 décembre 2023
P431 Steroid treatment may change natural history in congenital laminopathies
Neuromuscular disorders : NMD   01 octobre 2023
P342 An early onset benign myopathy with glycogen storage caused by a de novo 1.3 microdeletion of chromosome 14
Neuromuscular disorders : NMD   01 octobre 2023
MODISC: Evolution of Chronic Low Back Pain of Active Discopathy After Intradiscal Corticosteroid Infiltrations According to Modic 1 Distribution and Association With Degenerative Restructuring
Essai Clinique (Assistance publique – Hôpitaux de Paris)   18 septembre 2023
In-vivo characterization of the lumbar annulus fibrosus in adults with ultrasonography and shear wave elastography.
Medical engineering & physics   27 août 2023
An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 14.
Neuromuscular disorders : NMD   25 août 2023
Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis.
Journal of neurology   21 août 2023