Clemence Labasse

Paris, France

Last Updated: 09/26/2026

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Found 20 publications

Drug-induced autophagic myopathies: Exploring pathophysiology with immunolabelling and proteomics.

Drug-induced autophagic myopathies: Exploring pathophysiology with immunolabelling and proteomics.

Journal: Journal of neuropathology and experimental neurology

Published: January 29, 2026

Clinical, morphological, and molecular characterization of patients with X-linked myopathy with excessive autophagy (XMEA).

Clinical, morphological, and molecular characterization of patients with X-linked myopathy with excessive autophagy (XMEA).

Journal: Journal of neuropathology and experimental neurology

Published: November 27, 2025

Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review.

Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review.

Journal: Journal of neuromuscular diseases

Published: November 18, 2025

Psychosocial Determinants of Pain in Muscle Biopsy.

Psychosocial Determinants of Pain in Muscle Biopsy.

Journal: Muscle & nerve

Published: November 03, 2025

A novel XPNPEP3 gene variant manifesting as rhabdomyolysis and exercise intolerance.

A novel XPNPEP3 gene variant manifesting as rhabdomyolysis and exercise intolerance.

Journal: Journal of neuromuscular diseases

Published: September 15, 2025

Relevance of muscle biopsies in the neonatal and early infantile period: a 52 years retrospective study in the gene-sequencing era.

Relevance of muscle biopsies in the neonatal and early infantile period: a 52 years retrospective study in the gene-sequencing era.

Journal: Acta neuropathologica communications

Published: October 16, 2024

Pathogenic DPAGT1 variants in limb-girdle congenital myasthenic syndrome (LG-CMS) associated with tubular aggregates and ORAI1 hypoglycosylation.

Pathogenic DPAGT1 variants in limb-girdle congenital myasthenic syndrome (LG-CMS) associated with tubular aggregates and ORAI1 hypoglycosylation.

Journal: Neuropathology and applied neurobiology

Published: February 09, 2023

Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation.

Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation.

Journal: eLife

Published: October 12, 2022

Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies.

Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies.

Journal: Acta neuropathologica communications

Published: June 17, 2022

Congenital Nemaline Myopathy with Dense Protein Masses.

Congenital Nemaline Myopathy with Dense Protein Masses.

Journal: Journal of neuropathology and experimental neurology

Published: February 09, 2022

NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein Material.

NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein Material.

Journal: Journal of neuropathology and experimental neurology

Published: March 11, 2021

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

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

Journal: Acta neuropathologica communications

Published: July 24, 2019

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Last Updated: 09/26/2026