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Neurology
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Parkinson's disease/Parkinsonism

Citations 231-240 of 519 total displayed.

Past content (since Jan 2000):

ARTICLES
Dementia in Parkinson disease: Functional imaging of cholinergic and dopaminergic pathways
R. Hilker, A. V. Thomas, J. C. Klein, S. Weisenbach, E. Kalbe, L. Burghaus, A. H. Jacobs, K. Herholz, and W. D. Heiss
Neurology 2005; 65: 1716-1722. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Two patients with COMT inhibitor–induced hepatic dysfunction and UGT1A9 genetic polymorphism
E. Martignoni, M. Cosentino, M. Ferrari, G. Porta, E. Mattarucchi, F. Marino, S. Lecchini, and G. Nappi
Neurology 2005; 65: 1820-1822. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study
S. Karamohamed, J. C. Latourelle, B. A. Racette, J. S. Perlmutter, G. F. Wooten, M. Lew, C. Klein, H. Shill, L. I. Golbe, M. H. Mark, M. Guttman, G. Nicholson, J. B. Wilk, M. Saint-Hilaire, A. L. DeStefano, R. Prakash, S. Tobin, J. Williamson, O. Suchowersky, N. Labell, B.N.J. Growdon, C. Singer, R. Watts, S. Goldwurm, G. Pezzoli, K. B. Baker, M. L. Giroux, P. P. Pramstaller, D. J. Burn, P. Chinnery, S. Sherman, P. Vieregge, I. Litvan, J. F. Gusella, R. H. Myers, and A. Parsian
Neurology 2005; 65: 1823-1825. [Abstract] [Full text] [PDF]  

ARTICLES
Occupation and parkinsonism in three movement disorders clinics
S. M. Goldman, C. M. Tanner, C. W. Olanow, R. L. Watts, R. D. Field, and J. W. Langston
Neurology 2005; 65: 1430-1435. [Abstract] [Full text] [PDF]  

ARTICLES
Progression of motor impairment and disability in Parkinson disease: A population-based study
Guido Alves, Tore Wentzel-Larsen, Dag Aarsland, and Jan Petter Larsen
Neurology 2005; 65: 1436-1441. [Abstract] [Full text] [PDF]  

ARTICLES
Excessive daytime sleepiness and subsequent development of Parkinson disease
R. D. Abbott, G. W. Ross, L. R. White, C. M. Tanner, K. H. Masaki, J. S. Nelson, J. D. Curb, and H. Petrovitch
Neurology 2005; 65: 1442-1446. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Mutations in the glucocerebrosidase gene and Parkinson disease: Phenotype–genotype correlation
Judith Aharon-Peretz, Samih Badarny, Hanna Rosenbaum, and Ruth Gershoni-Baruch
Neurology 2005; 65: 1460-1461. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Long-term 24-hour duodenal infusion of levodopa: Outcome and dose requirements
Dag Nyholm, Rasmus Jansson, Thomas Willows, and Ingela Nilsson Remahl
Neurology 2005; 65: 1506-1507. [Full text] [PDF]  

REFLECTIONS: NEUROLOGY AND THE HUMANITIES
Editorial: PLEASE WRITE!
Michael H. Brooke
Neurology 2005; 65: 1511. [Full text] [PDF]  

ARTICLES
Familial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated population
M.J.E. van Rijn, A. J.C. Slooter, A. F.C. Schut, A. Isaacs, Y. S. Aulchenko, P. J.L.M. Snijders, L. J. Kappelle, J. C. van Swieten, B. A. Oostra, and C. M. van Duijn
Neurology 2005; 65: 1203-1209. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* 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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