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All Pediatric
Citations 211-220 of 280 total displayed.
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Past content
(since Jan 2001):
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- EDITORIALS
Another double trouble: Silent carriers of doublecortin mutations
- Joseph G. Gleeson
Neurology 2003; 60: 164-165.
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- SPECIAL ARTICLES
Practice parameter: Treatment of the child with a first unprovoked seizure: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
- D. Hirtz, A. Berg, D. Bettis, C. Camfield, P. Camfield, P. Crumrine, W. D. Gaillard, S. Schneider, and S. Shinnar
Neurology 2003; 60: 166-175.
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- ARTICLES
Spatial and motor neglect in children
- A. Laurent-Vannier, P. Pradat-Diehl, M. Chevignard, G. Abada, and M. De Agostini
Neurology 2003; 60: 202-207.
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- BRIEF COMMUNICATIONS
Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders
- L. Aigner, G. Uyanik, S. Couillard-Despres, S. Ploetz, G. Wolff, D. Morris-Rosendahl, P. Martin, U. Eckel, S. Spranger, J. Otte, H. Woerle, H. Holthausen, N. Apheshiotis, D. Fluegel, and J. Winkler
Neurology 2003; 60: 329-332.
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- CLINICAL/SCIENTIFIC NOTES
Multiphasic demyelinating disease involving central and peripheral nervous system in a child
- P. Mariotti, A.P. Batocchi, C. Colosimo, M. Lo Monaco, M. Caggiula, F. Colitto, P.A. Tonali, and F. Guzzetta
Neurology 2003; 60: 348-349.
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- ARTICLES
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy
- K. Vahedi, P. Massin, J.-P. Guichard, S. Miocque, M. Polivka, F. Goutières, D. Dress, F. Chapon, M.-M. Ruchoux, F. Riant, A. Joutel, A. Gaudric, M.-G. Bousser, and E. Tournier-Lasserve
Neurology 2003; 60: 57-63.
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- ARTICLES
fMRI identifies regional specialization of neural networks for reading in young children
- W.D. Gaillard, L.M. Balsamo, Z. Ibrahim, B.C. Sachs, and B. Xu
Neurology 2003; 60: 94-100.
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- EDITORIALS
Holoprosencephaly: The face predicts the brain; the image predicts its function
- Marc C. Patterson
Neurology 2002; 59: 1833-1834.
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- ARTICLES
Course and prognosis in early-onset MS: Comparison with adult-onset forms
- I. L. Simone, D. Carrara, C. Tortorella, M. Liguori, V. Lepore, F. Pellegrini, A. Bellacosa, A. Ceccarelli, I. Pavone, and P. Livrea
Neurology 2002; 59: 1922-1928.
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- BRIEF COMMUNICATIONS
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
- A. Fogli, C. Dionisi-Vici, F. Deodato, A. Bartuli, O. Boespflug-Tanguy, and E. Bertini
Neurology 2002; 59: 1966-1968.
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