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Parkinson's disease/Parkinsonism
Citations 1-10 of 463 total displayed.
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Most recent content
(6 Jan 2009):
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- ARTICLES
Frontal FDG-PET activity correlates with cognitive outcome after STN-DBS in Parkinson disease
- E. Kalbe, J. Voges, T. Weber, M. Haarer, S. Baudrexel, J. C. Klein, J. Kessler, V. Sturm, W. D. Heiss, and R. Hilker
Neurology 2009; 72: 42-49.
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Past content
(since Jan 2000):
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- ARTICLES
Is olfactory impairment in Parkinson disease related to phenotypic or genotypic characteristics?
- D. Verbaan, S. Boesveldt, S. M. van Rooden, M. Visser, J. Marinus, M. G. Macedo, Y. Fang, P. Heutink, H. W. Berendse, and J. J. van Hilten
Neurology 2008; 71: 1877-1882.
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- EDITORIALS
Early diagnosis of progressive supranuclear palsy: Bucking the odds
- Lawrence I. Golbe
Neurology 2008; 71: 1754-1755.
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- ARTICLES
Progression of dopaminergic dysfunction in a LRRK2 kindred: A multitracer PET study
- R. Nandhagopal, E. Mak, M. Schulzer, J. McKenzie, S. McCormick, V. Sossi, T. J. Ruth, A. Strongosky, M. J. Farrer, Z. K. Wszolek, and A. J. Stoessl
Neurology 2008; 71: 1790-1795.
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- ARTICLES
Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore
- C. H. Lin, E. K. Tan, M. L. Chen, L. C. Tan, H. Q. Lim, G. S. Chen, and R. M. Wu
Neurology 2008; 71: 1727-1732.
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- RESIDENT AND FELLOW SECTION
Teaching NeuroImage: MRI in multiple system atrophy: "Hot cross bun" sign and hyperintense rim bordering the putamina
- João Massano, Fernando Costa, and Goreti Nadais
Neurology 2008; 71: e38.
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- ARTICLES
Progranulin variability has no major role in Parkinson disease genetic etiology
- K. Nuytemans, P. Pals, K. Sleegers, S. Engelborghs, E. Corsmit, K. Peeters, B. Pickut, M. Mattheijssens, P. Cras, P. P. De Deyn, J. Theuns, and C. Van Broeckhoven
Neurology 2008; 71: 1147-1151.
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- ARTICLES
Hyposmia in G2019S LRRK2-related parkinsonism: Clinical and pathologic data
- L. Silveira-Moriyama, L. C. Guedes, A. Kingsbury, H. Ayling, K. Shaw, E. R. Barbosa, V. Bonifati, N. P. Quinn, P. Abou-Sleiman, N. W. Wood, A. Petrie, C. Sampaio, J. J. Ferreira, J. Holton, T. Revesz, and A. J. Lees
Neurology 2008; 71: 1021-1026.
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- ARTICLES
PINK1 mutations and parkinsonism
- L. Ishihara-Paul, M. M. Hulihan, J. Kachergus, R. Upmanyu, L. Warren, R. Amouri, R. Elango, R. K. Prinjha, A. Soto, M. Kefi, M. Zouari, S. B. Sassi, S. B. Yahmed, G. El Euch-Fayeche, P. M. Matthews, L. T. Middleton, R. A. Gibson, F. Hentati, and M. J. Farrer
Neurology 2008; 71: 896-902.
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- ARTICLES
Imaging amyloid deposition in Lewy body diseases
- S. N. Gomperts, D. M. Rentz, E. Moran, J. A. Becker, J. J. Locascio, W. E. Klunk, C. A. Mathis, D. R. Elmaleh, T. Shoup, A. J. Fischman, B. T. Hyman, J. H. Growdon, and K. A. Johnson
Neurology 2008; 71: 903-910.
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