The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene-Reference-Cited by-同舟云学术

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

Published:2007-02-04 Issue:3 Volume:130 Page:828-835
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Brashear A.,Dobyns W. B.,de Carvalho Aguiar P.,Borg M.,Frijns C. J. M.,Gollamudi S.,Green A.,Guimaraes J.,Haake B. C.,Klein C.,Linazasoro G.,Munchau A.,Raymond D.,Riley D.,Saunders-Pullman R.,Tijssen M. A. J.,Webb D.,Zaremba J.,Bressman S. B.,Ozelius L. J.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/130/3/828/778538/awl340.pdf

Reference24 articles.

1. Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonism

2. Rapid-onset dystonia-parkinsonism in a second family

3. Variable phenotype of rapid-onset dystonia-parkinsonism

4. PET imaging of the pre-synaptic dopamine uptake sites in rapid-onset dystonia-parkinsonism (RDP)

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