A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation-Reference-Cited by-同舟云学术

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A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation

Published:2007-07-23 Issue:4 Volume:69 Page:368-375
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Warnecke T.,Duning T.,Schwan A.,Lohmann H.,Epplen J. T.,Young P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 52 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An MRI evaluation of white matter involvement in paradigmatic forms of spastic ataxia: results from the multi-center PROSPAX study;Journal of Neurology;2024-06-16

2. Pluripotent Stem Cells as a Preclinical Cellular Model for Studying Hereditary Spastic Paraplegias;International Journal of Molecular Sciences;2024-02-23

3. Periodic Alternating Nystagmus, Ataxia, and Spasticity: A Unique Presentation of Spastic Paraplegia 7‐Related Hereditary Spastic Paraplegia;Movement Disorders Clinical Practice;2024-02-23

4. Neuroimaging in hereditary spastic paraplegias: from qualitative cues to precision biomarkers;Expert Review of Molecular Diagnostics;2022-07-03

5. Hereditary Spastic Paraplegia: An Update;International Journal of Molecular Sciences;2022-02-01

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