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All Pediatric
Citations 191-200 of 278 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
- R. Nabbout, E. Gennaro, B. Dalla Bernardina, O. Dulac, F. Madia, E. Bertini, G. Capovilla, C. Chiron, G. Cristofori, M. Elia, E. Fontana, R. Gaggero, T. Granata, R. Guerrini, M. Loi, L. La Selva, M. L. Lispi, A. Matricardi, A. Romeo, V. Tzolas, D. Valseriati, P. Veggiotti, F. Vigevano, L. Vallée, F. Dagna Bricarelli, A. Bianchi, and F. Zara
Neurology 2003; 60: 1961-1967.
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- BRIEF COMMUNICATIONS
A neuropathological, stereo-EEG, and MRI study of subcortical band heterotopia
- R. Mai, L. Tassi, M. Cossu, S. Francione, G. Lo Russo, R. Garbelli, A. Ferrario, C. Galli, F. Taroni, A. Citterio, and R. Spreafico
Neurology 2003; 60: 1834-1838.
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- EDITORIALS
Is language laterality established by 5 years of age?
- Anne L. Foundas
Neurology 2003; 60: 1573-1574.
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- ARTICLES
Auditory comprehension of language in young children: Neural networks identified with fMRI
- Z. Ahmad, L. M. Balsamo, B. C. Sachs, B. Xu, and W. D. Gaillard
Neurology 2003; 60: 1598-1605.
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- ARTICLES
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21
- A. Rajab, G. H. Mochida, A. Hill, V. Ganesh, A. Bodell, A. Riaz, P. E. Grant, Y. Y. Shugart, and C. A. Walsh
Neurology 2003; 60: 1664-1667.
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- CLINICAL/SCIENTIFIC NOTES
A child with spinal cord AVM presenting with raised intracranial pressure
- A. G. Bassuk, D. M. Burrowes, B. Velimirovic, J. Grant, and G. F. Keating
Neurology 2003; 60: 1724-1725.
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- VIEWS & REVIEWS
Clinical spectrum of succinic semialdehyde dehydrogenase deficiency
- P. L. Pearl, K. M. Gibson, M. T. Acosta, L. G. Vezina, W. H. Theodore, M. A. Rogawski, E. J. Novotny, A. Gropman, J. A. Conry, G. T. Berry, and M. Tuchman
Neurology 2003; 60: 1413-1417.
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- BRIEF COMMUNICATIONS
X-linked myotubular myopathy in a female infant caused by a new MTM1 gene mutation
- Ulrike Schara, Wolfram Kress, Jens Tücke, and Wilhelm Mortier
Neurology 2003; 60: 1363-1365.
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- ARTICLES
Autosomal recessive form of periventricular heterotopia
- V. L. Sheen, M. Topçu, S. Berkovic, D. Yalnizoglu, I. Blatt, A. Bodell, R. S. Hill, V. S. Ganesh, T. J. Cherry, Y. Y. Shugart, and C. A. Walsh
Neurology 2003; 60: 1108-1112.
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- ARTICLES
Natural history of cognitive deficits and their relationship to MRI T2-hyperintensities in NF1
- S.L. Hyman, D.S. Gill, E.A. Shores, A. Steinberg, P. Joy, S.V. Gibikote, and K.N. North
Neurology 2003; 60: 1139-1145.
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