Nathalie Streichenberger

Groupement Hospitalier Est
Lyon, France

Last Updated: 09/26/2026

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Found 107 publications

French National Protocol for Diagnosis and Care of Calpainopathy (LGMD R1/LGMD D4): consensus guidelines for clinical practice.

French National Protocol for Diagnosis and Care of Calpainopathy (LGMD R1/LGMD D4): consensus guidelines for clinical practice.

Journal: Orphanet journal of rare diseases

Published: December 16, 2025

Multiple Mononeuropathy Secondary to Parvovirus B19 Infection: A Case Series.

Multiple Mononeuropathy Secondary to Parvovirus B19 Infection: A Case Series.

Journal: European journal of neurology

Published: December 02, 2025

Challenging mtDNA tRNA variant guidelines: Emphasizing single-cell analysis through four novel variants.

Challenging mtDNA tRNA variant guidelines: Emphasizing single-cell analysis through four novel variants.

Journal: Mitochondrion

Published: November 15, 2025

NuMA1 controls myonuclear motility in striated skeletal muscle through AMPK activity and is impaired in Duchenne muscular dystrophy.

NuMA1 controls myonuclear motility in striated skeletal muscle through AMPK activity and is impaired in Duchenne muscular dystrophy.

Journal: Cell death & disease

Published: October 20, 2025

Interplay between microtubule interactome, myonuclei mechanotransduction, and positioning in myopathies.

Interplay between microtubule interactome, myonuclei mechanotransduction, and positioning in myopathies.

Journal: Nucleus (Austin, Tex.)

Published: July 03, 2025

Homozygous COQ9 mutation: a new cause of potentially treatable hereditary spastic paraplegia.

Homozygous COQ9 mutation: a new cause of potentially treatable hereditary spastic paraplegia.

Journal: European journal of human genetics : EJHG

Published: January 29, 2025

Contribution of major histocompatibility complex class II immunostaining in distinguishing idiopathic inflammatory myopathy subgroups: A histopathological cohort study.

Contribution of major histocompatibility complex class II immunostaining in distinguishing idiopathic inflammatory myopathy subgroups: A histopathological cohort study.

Journal: Journal of neuropathology and experimental neurology

Published: September 16, 2024

Mitochondrial disorders are associated with morphological neuromuscular junction defects.

Mitochondrial disorders are associated with morphological neuromuscular junction defects.

Journal: Neuromuscular disorders : NMD

Published: August 11, 2024

Prion diseases disrupt glutamate/glutamine metabolism in skeletal muscle.

Prion diseases disrupt glutamate/glutamine metabolism in skeletal muscle.

Journal: PLoS pathogens

Published: June 19, 2024

Defining the landscape of TIA1 and SQSTM1 digenic myopathy.

Defining the landscape of TIA1 and SQSTM1 digenic myopathy.

Journal: Neuromuscular disorders : NMD

Published: April 22, 2024

Granulomatous myositis: characteristics and outcome from a monocentric retrospective cohort study.

Granulomatous myositis: characteristics and outcome from a monocentric retrospective cohort study.

Journal: Neuromuscular disorders : NMD

Published: March 14, 2024

Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy.

Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy.

Journal: Acta neuropathologica

Published: February 27, 2024

Showing 1-12 of 107

Last Updated: 09/26/2026