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Neurology
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All Movement Disorders

Citations 41-50 of 174 total displayed.

Past content (since Jan 2000):

ARTICLES
Hemiparkinsonism-hemiatrophy syndrome
Subhashie Wijemanne and Joseph Jankovic
Neurology 2007; 69: 1585-1594. [Abstract] [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
Minimum incidence of primary cervical dystonia in a multiethnic health care population
C. Marras, S. K. Van den Eeden, R. D. Fross, K. S. Benedict-Albers, J. Klingman, A. D. Leimpeter, L. M. Nelson, N. Risch, A. J. Karter, A. L. Bernstein, and C. M. Tanner
Neurology 2007; 69: 676-680. [Abstract] [Full text] [PDF]  

ARTICLES
Genotype–phenotype correlation of paroxysmal nonkinesigenic dyskinesia
M. K. Bruno, H.-Y Lee, G.W.J. Auburger, A. Friedman, J. E. Nielsen, A. E. Lang, E. Bertini, P. Van Bogaert, Y. Averyanov, M. Hallett, K. Gwinn-Hardy, B. Sorenson, M. Pandolfo, H. Kwiecinski, S. Servidei, Y.-H Fu, and L. Ptácek
Neurology 2007; 68: 1782-1789. [Abstract] [Full text] [PDF]  

EDITORIALS
Clinical heterogeneity of ATP13A2 linked disease (Kufor-Rakeb) justifies a PARK designation
Andrew J. Lees and Andrew B. Singleton
Neurology 2007; 68: 1553-1554. [Full text] [PDF]  

ARTICLES
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
A. Di Fonzo, H. F. Chien, M. Socal, S. Giraudo, C. Tassorelli, G. Iliceto, G. Fabbrini, R. Marconi, E. Fincati, G. Abbruzzese, P. Marini, F. Squitieri, M. W. Horstink, P. Montagna, A. Dalla Libera, F. Stocchi, S. Goldwurm, J. J. Ferreira, G. Meco, E. Martignoni, L. Lopiano, L. B. Jardim, B. A. Oostra, E. R. Barbosa, The Italian Parkinson Genetics Network, and V. Bonifati
Neurology 2007; 68: 1557-1562. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Distinctive MRI findings in pallidopontonigral degeneration (PPND)
Andrew R. Frank, Zbigniew K. Wszolek, Clifford R. Jack, Jr, and Bradley F. Boeve
Neurology 2007; 68: 620-621. [Full text] [PDF]  

REVIEW ARTICLES
Neurologic phenotypes associated with acanthocytosis
R. H. Walker, H. H. Jung, C. Dobson-Stone, L. Rampoldi, A. Sano, F. Tison, and A. Danek
Neurology 2007; 68: 92-98. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Dihydropteridine reductase deficiency: Levodopa’s long-term effectiveness without dyskinesia
F. Sedel, M. J. Ribeiro, P. Remy, N. Blau, J. -M. Saudubray, and Y. Agid
Neurology 2006; 67: 2243-2245. [Abstract] [Full text] [PDF]  

ARTICLES
Brain metal concentrations in chronic liver failure patients with pallidal T1 MRI hyperintensity
K. J. Klos, J. E. Ahlskog, N. Kumar, S. Cambern, J. Butz, M. Burritt, R. D. Fealey, C. T. Cowl, J. E. Parisi, and K. A. Josephs
Neurology 2006; 67: 1984-1989. [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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