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Neurology
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Motor Control

Citations 1-10 of 31 total displayed.

Most recent content (10 Nov 2009):

ARTICLES
Children with autism show specific handwriting impairments
Christina T. Fuentes, Stewart H. Mostofsky, and Amy J. Bastian
Neurology 2009; 73: 1532-1537. [Abstract] [Full text] [PDF]  

Past content (since Apr 2003):

EDITORIALS
Can rehabilitation help ataxia?
Susanne M. Morton and Amy J. Bastian
Neurology first published on October 28, 2009 as doi: WNL.0b013e3181c33b21. Rapid PDF  

ARTICLES
Intensive coordinative training improves motor performance in degenerative cerebellar disease
W. Ilg, M. Synofzik, D. Brötz, S. Burkard, M. A. Giese, and L. Schöls
Neurology first published on October 28, 2009 as doi: WNL.0b013e3181c33adf. [Abstract] Rapid PDF  

CLINICAL/SCIENTIFIC NOTES
FAMILIAL CONGENITAL MIRROR MOVEMENTS: REPORT OF A LARGE 4-GENERATION FAMILY
M. Srour, M. Philibert, M. -H. Dion, A. Duquette, F. Richer, G. A. Rouleau, and S. Chouinard
Neurology 2009; 73: 729-731. [Full text] [PDF]  

RESIDENT AND FELLOW SECTION
Emerging Subspecialties in Neurology: Translational research in movement disorders
Sheng-Han Kuo and George R. Jackson
Neurology 2009; 73: e40-41e. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
PARADOXICAL FACILITATION: THE RESOLUTION OF FOREIGN ACCENT SYNDROME AFTER CEREBELLAR STROKE
D. A. Cohen, K. Kurowski, M. S. Steven, S. E. Blumstein, and A. Pascual-Leone
Neurology 2009; 73: 566-567. [Full text] [PDF]  

EDITORIALS
A new sensitive imaging biomarker for Parkinson disease?
Anthony E. Lang and David Mikulis
Neurology 2009; 72: 1374-1375. [Full text] [PDF]  

ARTICLES
High-resolution diffusion tensor imaging in the substantia nigra of de novo Parkinson disease
D. E. Vaillancourt, M. B. Spraker, J. Prodoehl, I. Abraham, D. M. Corcos, X. J. Zhou, C. L. Comella, and D. M. Little
Neurology 2009; 72: 1378-1384. [Abstract] [Full text] [PDF]  

EDITORIALS
Subclinical cortical reorganization: A preclinical imaging marker for recessively inherited PD?
Lin Zhang
Neurology 2009; 72: 1036-1037. [Full text] [PDF]  

ARTICLES
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype
B.F.L. van Nuenen, M. M. Weiss, B. R. Bloem, K. Reetz, T. van Eimeren, K. Lohmann, J. Hagenah, P. P. Pramstaller, F. Binkofski, C. Klein, and H. R. Siebner
Neurology 2009; 72: 1041-1047. [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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