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Neurology, Vol. 65, Issue 5, 664-665, September 13, 2005

EDITORIALS

LRRK2: Both a cause and a risk factor for Parkinson disease?

Tatiana Foroud

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September 13 Highlights
Neurology 2005 65: 660-661. [Full Text] [PDF]

LRRK2 gene in Parkinson disease: Mutation analysis and case control association study
C. Paisán-Ruíz, A. E. Lang, T. Kawarai, C. Sato, S. Salehi-Rad, G. K. Fisman, T. Al-Khairallah, P. St George-Hyslop, A. Singleton, and E. Rogaeva
Neurology 2005 65: 696-700. [Abstract] [Full Text] [PDF]

LRRK2 mutations in Parkinson disease
M. Farrer, J. Stone, I. F. Mata, S. Lincoln, J. Kachergus, M. Hulihan, K. J. Strain, and D. M. Maraganore
Neurology 2005 65: 738-740. [Abstract] [Full Text] [PDF]

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations
C. P. Zabetian, A. Samii, A. D. Mosley, J. W. Roberts, B. C. Leis, D. Yearout, W. H. Raskind, and A. Griffith
Neurology 2005 65: 741-744. [Abstract] [Full Text] [PDF]



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 Proc. Natl. Acad. Sci. USAHome page
W. W. Smith, Z. Pei, H. Jiang, D. J. Moore, Y. Liang, A. B. West, V. L. Dawson, T. M. Dawson, and C. A. Ross
Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration
PNAS, December 20, 2005; 102(51): 18676 - 18681.
[Abstract] [Full Text] [PDF]

This Article
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