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All Clinical Neurology
Citations 11-20 of 226 total displayed.
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Past content
(since Mar 2001):
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- ARTICLES
Neural damage associated with atopic diathesis: A nationwide survey in Japan
- N. Isobe, J. Kira, N. Kawamura, T. Ishizu, K. Arimura, and Y. Kawano
Neurology 2009; 73: 790-797.
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- ARTICLES
Using fast eye movements to study fatigue in multiple sclerosis
- M. Matta, R. J. Leigh, M. Pugliatti, I. Aiello, and A. Serra
Neurology 2009; 73: 798-804.
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- MEDICAL HYPOTHESIS
ALS motor phenotype heterogeneity, focality, and spread: Deconstructing motor neuron degeneration
- John M. Ravits and Albert R. La Spada
Neurology 2009; 73: 805-811.
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- ARTICLES
Detection of anti-MAG antibodies in polyneuropathy associated with IgM monoclonal gammopathy
- M. L. Kuijf, M. Eurelings, A. P. Tio-Gillen, P. A. van Doorn, L. H. van den Berg, H. Hooijkaas, J. Stork, N. C. Notermans, and B. C. Jacobs
Neurology 2009; 73: 688-695.
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- 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.
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- CLINICAL/SCIENTIFIC NOTES
AKINETOPSIA IN THE POSTERIOR CORTICAL VARIANT OF ALZHEIMER DISEASE
- Po-Heng Tsai and Mario F. Mendez
Neurology 2009; 73: 731-732.
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- RESIDENT AND FELLOW SECTION
Clinical Reasoning: A 35-year-old man with a right hemiplegia and a cerebral mass
- G. Moretta, J. P. Pettinicchi, M. E. Talarico, P. A. Lopez, S. Cerrato, M. E. Balbuena, J. J. Poderoso, O. Mazzocchi, A. Dal Verme, C. Menghi, M. Arcavi, M. P. Grecco, and J. L. Ferreiro
Neurology 2009; 73: e35-38e.
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- EDITORIALS
No kidding: High risk of cognitive difficulty in new-onset pediatric epilepsy
- David W. Loring and Kimford J. Meador
Neurology 2009; 73: 496-497.
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- ARTICLES
Neuropsychological status at seizure onset in children: Risk factors for early cognitive deficits
- P. S. Fastenau, C. S. Johnson, S. M. Perkins, A. W. Byars, T. J. deGrauw, J. K. Austin, and D. W. Dunn
Neurology 2009; 73: 526-534.
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- ARTICLES
Consequences of mutations within the C terminus of the FHL1 gene
- B. Schoser, H. H. Goebel, I. Janisch, S. Quasthoff, J. Rother, M. Bergmann, W. Müller-Felber, and C. Windpassinger
Neurology 2009; 73: 543-551.
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