Funding agencies: This work was undertaken at UCLH/UCL, which received a proportion of funding from the Department of Health's NIHR Biomedical Research Centres funding scheme.
Article first published online: 2 NOV 2012
Copyright © 2012 Movement Disorder Society
Volume 27, Issue 14, pages 1769–1774, December 2012
How to Cite
Rubio-Agusti, I., Kojovic, M., Edwards, M. J., Murphy, E., Chandrashekar, H. S., Lachmann, R. H. and Bhatia, K. P. (2012), Atypical parkinsonism and cerebrotendinous xanthomatosis: Report of a family with corticobasal syndrome and a literature review. Mov. Disord., 27: 1769–1774. doi: 10.1002/mds.25229
Relevant conflicts of interest/financial disclosures: Nothing to report.
Full financial disclosures and author roles may be found in the online version of this article.
- Issue published online: 31 DEC 2012
- Article first published online: 2 NOV 2012
- Manuscript Accepted: 4 SEP 2012
- Manuscript Revised: 27 AUG 2012
- Manuscript Received: 9 FEB 2012
This article has been cited by:
- 1A suspicion index for early diagnosis and treatment of cerebrotendinous xanthomatosis, Journal of Inherited Metabolic Disease, 2014, 37, 3, 421, , , ,
- 2Parkinsonism and inborn errors of metabolism, Journal of Inherited Metabolic Disease, 2014, 37, 4, 627, ,
- 4Atypical parkinsonism, Current Opinion in Neurology, 2013, 26, 4, 401, ,
- 5Treatable inborn errors of metabolism causing neurological symptoms in adults, Molecular Genetics and Metabolism, 2013, 110, 4, 431, , , ,