Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2-Reference-Cited by-同舟云学术

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Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2

Published:1996 Issue:5 Volume:119 Page:1487-1496
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Dürr A.,Davoine C.-S.,Paternotte C.,von Fellenberg J.,Cogilnicean S.,Coutinho P.,Lamy C.,Bourgeois S.,Prud'homme J.-F.,Penet C.,Mas J.-L.,Burgunder J.-M.,Hazan J.,Weissenbach J.,Brice A.,Fontaine B.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/119/5/1487/1051733/119-5-1487.pdf

Cited by 76 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. Long-term progression of clinician-reported and gait performance outcomes in hereditary spastic paraplegias;Frontiers in Neuroscience;2023-09-22

2. Identification of c.1495C > T mutation in SPAST gene in a family of Han Chinese with hereditary spastic paraplegia;Neuroscience Letters;2023-08

3. Static Balance in Hereditary Spastic Paraplegias: a Cross-sectional Study;The Cerebellum;2023-01-24

4. Multiple sclerosis in patients with hereditary spastic paraplegia: a case report and systematic review;Neurological Sciences;2022-05-21

5. Genetics in hereditary spastic paraplegias: Essential but not enough;Current Opinion in Neurobiology;2022-02

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