Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation-Reference-Cited by-同舟云学术

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Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation

Published:2003-11-26 Issue:6 Volume:54 Page:748-759
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

McDermott Christopher J.,Grierson Andrew J.,Wood Jonathan D.,Bingley Megan,Wharton Stephen B.,Bushby Katharine M. D.,Shaw Pamela J.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference37 articles.

1. Hereditary spastic paraparesis: a review of new developments

2. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

3. Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

4. Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

5. A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)

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1. Novel de novo SPAST mutation in a Han Chinese SPG4 patient: a case report;Frontiers in Genetics;2024-07-30

2. Spastin and alsin protein interactome analyses begin to reveal key canonical pathways and suggest novel druggable targets;Neural Regeneration Research;2024-05-13

3. Novel genetic variant in hereditary spastic paraparesis;BMJ Case Reports;2024-04

4. Inhibition of spastin impairs motor function recovery after spinal cord injury;Brain Research Bulletin;2023-12

5. Converging Role for REEP1/SPG31 in Oxidative Stress;International Journal of Molecular Sciences;2023-02-09

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