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Neurology
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Basal ganglia

Citations 21-30 of 36 total displayed.

Past content (since Mar 2003):

ARTICLES
Homoplasmy, heteroplasmy, and mitochondrial dystonia
R. McFarland, P. F. Chinnery, E. L. Blakely, A. M. Schaefer, A.A.M. Morris, S. M. Foster, H. A.L. Tuppen, V. Ramesh, P. J. Dorman, D. M. Turnbull, and R. W. Taylor
Neurology 2007; 69: 911-916. [Abstract] [Full text] [PDF]  

EDITORIALS
The ARX story: A new twist
Cecil D. Hahn
Neurology 2007; 69: 421-422. [Full text] [PDF]  

EDITORIALS
Writer’s cramp: Questions of causation
Joel S. Perlmutter and W. Thomas Thach
Neurology 2007; 69: 331-332. [Full text] [PDF]  

ARTICLES
Structural abnormalities in the cerebellum and sensorimotor circuit in writer's cramp
C. Delmaire, M. Vidailhet, A. Elbaz, F. Bourdain, J. P. Bleton, S. Sangla, S. Meunier, A. Terrier, and S. Lehéricy
Neurology 2007; 69: 376-380. [Abstract] [Full text] [PDF]  

ARTICLES
Hypomyelination with atrophy of the basal ganglia and cerebellum: Follow-up and pathology
M. S. van der Knaap, T. Linnankivi, A. Paetau, A. Feigenbaum, K. Wakusawa, K. Haginoya, W. Köhler, M. Henneke, A. Dinopoulos, P. Grattan-Smith, K. Brockmann, R. Schiffmann, and S. Blaser
Neurology 2007; 69: 166-171. [Abstract] [Full text] [PDF]  

RESIDENT AND FELLOW PAGE
Symmetric basal ganglia calcification in a 9-year-old child with MELAS
Sheng-Horng Chung, Shyr-Chyr Chen, Wen-Jone Chen, and Chien-Chang Lee
Neurology 2005; 65: E19. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement
P. Maciel, V. T. Cruz, M. Constante, I. Iniesta, M. C. Costa, S. Gallati, N. Sousa, J. Sequeiros, P. Coutinho, and M. M. Santos
Neurology 2005; 65: 603-605. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Bi-hemispheric anterior cerebral artery with drop attacks and limb shaking TIAs
Elizabeth Gerstner, Bernardo Liberato, and Clinton B. Wright
Neurology 2005; 65: 174. [Full text] [PDF]  

ARTICLES
Sonographic detection of basal ganglia lesions in asymptomatic and symptomatic Wilson disease
U. Walter, K. Krolikowski, B. Tarnacka, R. Benecke, A. Czlonkowska, and D. Dressler
Neurology 2005; 64: 1726-1732. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)
J. R.M. Oliveira, E. Spiteri, M. J. Sobrido, S. Hopfer, J. Klepper, T. Voit, J. Gilbert, Z. K. Wszolek, D. B. Calne, A. J. Stoessl, M. Hutton, B. V. Manyam, F. Boller, M. Baquero, and D. H. Geschwind
Neurology 2004; 63: 2165-2167. [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
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 Botulinum toxin
 Multiple system atrophy
 Rett Syndrome
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