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Parkinson's disease/Parkinsonism
Citations 51-60 of 519 total displayed.
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Past content
(since Jan 2000):
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- ARTICLES
Incidence and remaining lifetime risk of Parkinson disease in advanced age
- Jane A. Driver, Giancarlo Logroscino, J. Michael Gaziano, and Tobias Kurth
Neurology 2009; 72: 432-438.
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- ARTICLES
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset
- W. C. Nichols, N. Pankratz, D. K. Marek, M. W. Pauciulo, V. E. Elsaesser, C. A. Halter, A. Rudolph, J. Wojcieszek, R. F. Pfeiffer, T. Foroud For the Parkinson Study Group–PROGENI Investigators
Neurology 2009; 72: 310-316.
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- ARTICLES
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome
- A. Di Fonzo, M.C.J. Dekker, P. Montagna, A. Baruzzi, E. H. Yonova, L. Correia Guedes, A. Szczerbinska, T. Zhao, L. O.M. Dubbel-Hulsman, C. H. Wouters, E. de Graaff, W. J.G. Oyen, E. J. Simons, G. J. Breedveld, B. A. Oostra, M. W. Horstink, and V. Bonifati
Neurology 2009; 72: 240-245.
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- CLINICAL/SCIENTIFIC NOTES
INFLAMMATORY PSEUDOTUMOR ASSOCIATED WITH HIV, JCV, AND IMMUNE RECONSTITUTION SYNDROME
- A. Gonzalez-Duarte, S. Sullivan, G. J. Sips, T. Naidich, G. Kleinman, J. Murray, S. Morgello, I. Germano, M. Mullen, and D. Simpson
Neurology 2009; 72: 289-290.
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- EDITORIALS
Parkinson disease(s): Is "Parkin disease" a distinct clinical entity?
- Christine Klein and Katja Lohmann
Neurology 2009; 72: 106-107.
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- ARTICLES
A multidisciplinary study of patients with early-onset PD with and without parkin mutations
- E. Lohmann, S. Thobois, S. Lesage, E. Broussolle, S. Tezenas du Montcel, M. -J. Ribeiro, P. Remy, A. Pelissolo, B. Dubois, L. Mallet, P. Pollak, Y. Agid, A. Brice, and The French Parkinson's Disease Genetics Study Group
Neurology 2009; 72: 110-116.
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- ARTICLE
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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- 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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