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Last Updated: 10/31/2025
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Found 133 publications
AAV8-based gene replacement therapy for hereditary spastic paraplegia type 5.
Journal: Molecular therapy. Methods & clinical development
Published: May 16, 2025
Expanding the Phenotypic Spectrum of SPG7 Rare Damaging Variants: Insights From a Hungarian Cohort.
Journal: Clinical genetics
Published: October 24, 2024
Spinal cord cross sign: a potential marker for hereditary spastic paraplegia type 5.
Journal: Neuroradiology
Published: June 14, 2024
Serine Palmitoyltransferase (SPT)-related Neurodegenerative and Neurodevelopmental Disorders.
Journal: Journal of neuromuscular diseases
Published: May 24, 2024
An MRI evaluation of white matter involvement in paradigmatic forms of spastic ataxia: results from the multi-center PROSPAX study.
Journal: Journal of neurology
Published: May 03, 2024
MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 13, 2024
Relationship between brain white matter damage and grey matter atrophy in hereditary spastic paraplegia types 4 and 5.
Journal: European journal of neurology
Published: January 09, 2024
Vitamin D3 deficiency and osteopenia in spastic paraplegia type 5 indicate impaired bone homeostasis.
Journal: Scientific reports
Published: July 24, 2023
Long-term progression of clinician-reported and gait performance outcomes in hereditary spastic paraplegias.
Journal: Frontiers in neuroscience
Published: May 21, 2023
A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A.
Journal: Journal of neurology
Published: May 09, 2023
Last Updated: 10/31/2025