Associated Papers
Dorsolateral Cervical Cord T2 Hyperintensity in KIF1C-Related Disease (Spastic Paraplegia 58): Two Long-Duration Cases.
Mitsutake A et al.
Annals of Clinical and Translational Neurology, 2025
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.
Zhi Y et al.
Cns Neuroscience & Therapeutics, 2025
39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG58
Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype.
Mahale R et al.
Acta Neurologica Belgica, 2024
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.
Yücel-Yılmaz D et al.
Brain & Development, 2018
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