Jean P. Pouget
Marseille, France
Last Updated: 09/26/2026
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Found 85 publications
Clinical and genetic features of patients suffering from CMT4J.
Journal: Journal of neurology
Published: July 25, 2023
Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry).
Journal: Orphanet journal of rare diseases
Published: April 21, 2020
New insights into the structural properties of κ-(BEDT-TTF)2Ag2(CN)3 spin liquid.
Journal: Acta crystallographica Section B, Structural science, crystal engineering and materials
Published: December 11, 2019
Novel CAPN3 variant associated with an autosomal dominant calpainopathy.
Journal: Neuropathology and applied neurobiology
Published: October 01, 2019
Characteristics of patients with vitamin B12-responsive neuropathy: a case series with systematic repeated electrophysiological assessment.
Journal: Neurological research
Published: March 20, 2019
Efficacy and Safety of Octagam® in Patients With Chronic Inflammatory Demyelinating Polyneuropathy.
Journal: Neurology and therapy
Published: January 10, 2019
Towards an harmonization of diagnosis by NGS of neuromuscular diseases - Actions of the Molecular Genetics sub-group of FILNEMUS
Journal: Medecine sciences : M/S
Published: November 13, 2018
Diagnostic odyssey at the heart of the 3rd National Initiative for Rare Disorders
Journal: Medecine sciences : M/S
Published: November 13, 2018
Last Updated: 09/26/2026