SPG15: a cause of juvenile atypical levodopa responsive parkinsonism-Reference-Cited by-同舟云学术

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SPG15: a cause of juvenile atypical levodopa responsive parkinsonism

Published:2013-12-24 Issue:2 Volume:261 Page:435-437
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Mallaret Martial,Lagha-Boukbiza Ouhaid,Biskup Saskia,Namer Izzie Jacques,Rudolf Gabrielle,Anheim Mathieu,Tranchant Christine

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-013-7216-4.pdf

Reference7 articles.

1. Hanein S, Martin E, Boukhris A et al (2008) Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am J Hum Genet 82:992–1002

2. Schicks J, Synofzik M, Pétursson H et al (2011) Atypical juvenile parkinsonism in a consanguineous SPG15 family. Mov Disord 26:564–566

3. Goizet C, Boukhris A, Maltete D et al (2009) SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. Neurology 73:1111–1119

4. Paisán-Ruiz C, Guevara R, Federoff M et al (2010) Early-onset L-dopa responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Mov Disord 25:1791–1800

5. Anheim M, Lagier-Tourenne C, Stevanin G et al (2009) SPG11 spastic paraplegia. A new cause of juvenile parkinsonism. J Neurol 256:104–108

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