Last Updated: 09/26/2026
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Found 91 publications
Mutation-specific cellular mechanisms in Drosophila models of ATL1-associated hereditary spastic paraplegia.
Journal: Neurobiology of disease
Published: April 28, 2026
Dynamic conformational ensembles of soluble Tau encode neuronal toxicity prior to aggregation.
Journal: bioRxiv : the preprint server for biology
Published: February 09, 2026
LXR agonist rescues synaptic dysfunction and degeneration in SPG3A patient-specific iPSC-derived neurons.
Journal: Acta neuropathologica communications
Published: June 17, 2025
Editorial: Translational research in hereditary spastic paraplegias: filling the diagnosis gap and therapeutic perspectives.
Journal: Frontiers in neuroscience
Published: March 18, 2025
Small peptide P110 mitigates axonal degeneration of SPG15 patient iPSC-derived neurons by targeting mitochondrial dysfunction.
Journal: Neurobiology of disease
Published: March 17, 2025
Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration.
Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration.
Journal: Annals of clinical and translational neurology
Published: February 04, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic Paraplegia.
Journal: Neurology. Genetics
Published: September 26, 2024
A depression-associated protein FKBP5 functions in autophagy initiation through scaffolding the VPS34 complex.
Journal: Molecular neurobiology
Published: July 16, 2024
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Journal: Neurobiology of disease
Published: January 13, 2024
Last Updated: 09/26/2026