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LEFEUVRE , Claire

Last name: LEFEUVRE

First name: Claire

2019 (v1)

Journal article

Metadata-only

Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment

Laforêt, Pascal Inoue, Michio Goillot, Evelyne

International audience

Uploaded on: December 4, 2022
2024 (v1)

Journal article

Metadata-only

Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry

Retailleau, Emilie Lefeuvre, Claire de Antonio, Marie

© 2024 The Author(s). European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.Background and purpose: Late onset Pompe disease (LOPD) is a rare neuromuscular disorder caused by a deficit in acid alpha-glucosidase. Macroglossia and swallowing disorders have already been reported, but no study...

Uploaded on: September 5, 2024