Stephanie Millecamps
Paris, 75013, France
Last Updated: 09/26/2026
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Found 49 publications
Familial, neuropathological and cellular analysis identify ARPP21 as a major amyotrophic lateral sclerosis associated gene in French cohorts.
Journal: Acta neuropathologica
Published: May 11, 2026
Neuropathological analysis of an ALS patient carrying a SOD1 missense variant and a C9orf72 repeat expansion.
Journal: Acta neuropathologica
Published: October 14, 2025
MAPT mutations in amyotrophic lateral sclerosis: clinical, neuropathological and functional insights.
Journal: Journal of neurology
Published: November 04, 2024
EVolution in ALS diagnosis: molecular markers in extracellular vesicles.
Journal: Trends in molecular medicine
Published: July 11, 2024
ALS/FTD-linked TBK1 deficiency in microglia induces an aged-like microglial signature and drives social recognition deficits in mice.
Journal: Nature communications
Published: July 06, 2024
Dysregulation of muscle cholesterol transport in amyotrophic lateral sclerosis.
Journal: Brain : a journal of neurology
Published: February 16, 2024
Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes.
Journal: Nature communications
Published: December 04, 2023
Heterozygous SPTLC1 p.Leu39del is a major cause of slow-progressing juvenile ALS.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: April 28, 2023
Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells.
Journal: Brain : a journal of neurology
Published: December 08, 2022
Neurofilament accumulations in amyotrophic lateral sclerosis patients' motor neurons impair axonal initial segment integrity.
Journal: Cellular and molecular life sciences : CMLS
Published: November 04, 2022
The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis.
Journal: International journal of molecular sciences
Published: April 29, 2022
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
Journal: Nature genetics
Published: February 01, 2022
Last Updated: 09/26/2026