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Neurology
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Parkinson's disease/Parkinsonism

Citations 121-130 of 519 total displayed.

Past content (since Jan 2000):

ARTICLES
Neurocirculatory and nigrostriatal abnormalities in Parkinson disease from LRRK2 mutation
D. S. Goldstein, R. Imrich, E. Peckham, C. Holmes, G. Lopez, C. Crews, J. Hardy, A. Singleton, and M. Hallett
Neurology 2007; 69: 1580-1584. [Abstract] [Full text] [PDF]  

ARTICLES
Hemiparkinsonism-hemiatrophy syndrome
Subhashie Wijemanne and Joseph Jankovic
Neurology 2007; 69: 1585-1594. [Abstract] [Full text] [PDF]  

ARTICLES
The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: Is there a gender effect?
A. Orr-Urtreger, C. Shifrin, U. Rozovski, S. Rosner, D. Bercovich, T. Gurevich, H. Yagev-More, A. Bar-Shira, and N. Giladi
Neurology 2007; 69: 1595-1602. [Abstract] [Full text] [PDF]  

ARTICLES
Predictors of fitness to drive in people with Parkinson disease
H. Devos, W. Vandenberghe, A. Nieuwboer, M. Tant, G. Baten, and W. De Weerdt
Neurology 2007; 69: 1434-1441. [Abstract] [Full text] [PDF]  

ARTICLES
Reduced cardiac 123I-MIBG uptake reflects cardiac sympathetic dysfunction in Lewy body disease
H. Oka, M. Yoshioka, M. Morita, K. Onouchi, M. Suzuki, Y. Ito, T. Hirai, S. Mochio, and K. Inoue
Neurology 2007; 69: 1460-1465. [Abstract] [Full text] [PDF]  

REFLECTIONS: NEUROLOGY AND THE HUMANITIES
Black substance
Dawn McGuire
Neurology 2007; 69: 1380. [Full text] [PDF]  

ARTICLES
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease
L. N. Clark, B. M. Ross, Y. Wang, H. Mejia-Santana, J. Harris, E. D. Louis, L. J. Cote, H. Andrews, S. Fahn, C. Waters, B. Ford, S. Frucht, R. Ottman, and K. Marder
Neurology 2007; 69: 1270-1277. [Abstract] [Full text] [PDF]  

ARTICLES
San Francisco/Oakland Bay Bridge Welder Study: Olfactory function
Marcelo B. Antunes, Rosemarie Bowler, and Richard L. Doty
Neurology 2007; 69: 1278-1284. [Abstract] [Full text] [PDF]  

ARTICLES
Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease
P. T. Luoma, J. Eerola, S. Ahola, A. H. Hakonen, O. Hellström, K. T. Kivistö, P. J. Tienari, and A. Suomalainen
Neurology 2007; 69: 1152-1159. [Abstract] [Full text] [PDF]  

ARTICLES
Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia
F. Binkofski, K. Reetz, C. Gaser, R. Hilker, J. Hagenah, K. Hedrich, T. van Eimeren, A. Thiel, C. Büchel, P. P. Pramstaller, H. R. Siebner, and C. Klein
Neurology 2007; 69: 842-850. [Abstract] [Full text] [PDF]  

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* Related collections:
 Movement Disorders
 All Movement Disorders
 Dystonia
 Blepharospasm
 Gait disorders/ataxia
 Cerebellum
 Huntington's disease
 Basal ganglia
 Parkinson's disease/Parkinsonism
 Motor Control
 Progressive supranuclear palsy
 Motor cortex
 Stiff person syndrome
 Surgery/Stimulation
 Tourette syndrome
 Tremor
 Tics
 Chorea
 Botulinum toxin
 Multiple system atrophy
 Rett Syndrome
 Myoclonus
 Spastic paraplegia


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