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All Pediatric
Citations 131-140 of 280 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Clinical significance of isolated hippocampal volume asymmetry in childhood epilepsy
- P. Major, J.-C. Décarie, A. Nadeau, P. Diadori, A. Lortie, D. Nguyen, P. Cossette, and L. Carmant
Neurology 2004; 63: 1503-1506.
[Abstract]
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- VIEWS & REVIEWS
FDA-approved neurologic devices intended for use in infants, children, and adolescents
- Carlos Peña, Kristen Bowsher, and Joy Samuels-Reid
Neurology 2004; 63: 1163-1167.
[Abstract]
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- BRIEF COMMUNICATIONS
Differential localization of hamartin and tuberin and increased S6 phosphorylation in a tuber
- F. E. Jansen, R. G.E. Notenboom, M. Nellist, M. A. Goedbloed, D. J. Halley, P. N.E. de Graan, and O. van Nieuwenhuizen
Neurology 2004; 63: 1293-1295.
[Abstract]
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- ARTICLES
Status epilepticus after the initial diagnosis of epilepsy in children
- A. T. Berg, S. Shinnar, F. M. Testa, S. R. Levy, D. Frobish, S. N. Smith, and B. Beckerman
Neurology 2004; 63: 1027-1034.
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- ARTICLES
Language cortex activation in normal children
- A. G. Wood, A. S. Harvey, R. M. Wellard, D. F. Abbott, V. Anderson, M. Kean, M. M. Saling, and G. D. Jackson
Neurology 2004; 63: 1035-1044.
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- ARTICLES
ABILHAND-Kids: A measure of manual ability in children with cerebral palsy
- Carlyne Arnould, Massimo Penta, Anne Renders, and Jean-Louis Thonnard
Neurology 2004; 63: 1045-1052.
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- NEUROIMAGES
MRI in acute intermittent maple syrup urine disease
- M. Di Rocco, R. Biancheri, A. Rossi, A. E.M. Allegri, V. Vecchi, and P. Tortori-Donati
Neurology 2004; 63: 1078.
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- BRIEF COMMUNICATIONS
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy
- P. Prandini, A. Berardinelli, M. Fanin, F. Morello, E. Zardini, A. Pichiecchio, C. Uggetti, G. Lanzi, C. Angelini, and E. Pegoraro
Neurology 2004; 63: 1118-1121.
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- VIEWS & REVIEWS
Krabbe disease: Neurophysiologic studies and MRI correlations
- Aatif M. Husain, Maha Altuwaijri, and Mohammed Aldosari
Neurology 2004; 63: 617-620.
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- BRIEF COMMUNICATIONS
Cortical malformations are associated with a rare polymorphism of cellular prion protein
- R. Walz, R. M.R.P.S. Castro, M. C. Landemberger, T. R. Velasco, V. C. Terra-Bustamante, A. C. Bastos, M. Bianchin, L. Wichert-Ana, D. Araújo, V. Alexandre, Jr., A. C. Santos, H. R. Machado, C. G. Carlotti, Jr., R. R. Brentani, V. R. Martins, and A. C. Sakamoto
Neurology 2004; 63: 557-560.
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