Nathalie Streichenberger
Researcher
Lyon College
faculty
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Biography and Research Information
OverviewAI-generated summary
Dr. Nathalie Streichenberger's research encompasses inflammatory myopathies, prion diseases, sarcoidosis, and glioma. Her work addresses muscle physiology, protein misfolding, and the diagnosis and treatment of cancers. Streichenberger's most recent publication was in 2025.
Metrics
- h-index: 47
- Publications: 234
- Citations: 7,076
Selected Publications
- Interplay between microtubule interactome, myonuclei mechanotransduction, and positioning in myopathies (2025) DOI
- Homozygous COQ9 mutation: a new cause of potentially treatable hereditary spastic paraplegia (2025) DOI
- Myosites granulomateuses et hypercalcémie : une entité spécifique? À partir d’une série de cas et revue de la littérature (2024) DOI
- Mitochondrial disorders are associated with morphological neuromuscular junction defects (2024) DOI
- Contribution of major histocompatibility complex class II immunostaining in distinguishing idiopathic inflammatory myopathy subgroups: A histopathological cohort study (2024) DOI
- Prion diseases disrupt glutamate/glutamine metabolism in skeletal muscle (2024) DOI
- Defining the landscape of TIA1 and SQSTM1 digenic myopathy (2024) DOI
- Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy (2024) DOI
- P-223 PROMIND - PROMOTING MENTAL HEALTH AT WORK FOR HEALTHCARE PROFESSIONALS: PARTICIPATORY DEVELOPMENT OF A MINDFULNESS MEDITATION PROGRAM ADAPTED TO THE FRENCH HOSPITAL WORKPLACE (2024) DOI
- Granulomatous myositis: characteristics and outcome from a monocentric retrospective cohort study (2024) DOI
- Author Reply to Peer Reviews of Prion diseases disrupt the glutamate/glutamine metabolism in skeletal muscle (2024) DOI
- Predictors of Progression in a Series of 81 Adult Patients Surgically Managed for an Intracranial Hemangioblastoma: Implications for the Postoperative Follow-Up (2024) DOI
- H2A.Z is involved in premature aging and DSB repair initiation in muscle fibers (2024) DOI
- Mononeuritis multiplex following immune checkpoint inhibitors in malignant pleural mesothelioma (2024) DOI
- Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation. (2023) DOI
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