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All Pediatric
Citations 141-150 of 280 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Progressive myoclonus epilepsy with polyglucosans (Lafora disease): Evidence for a third locus
- E. M. Chan, S. Omer, M. Ahmed, L. R. Bridges, C. Bennett, S. W. Scherer, and B. A. Minassian
Neurology 2004; 63: 565-567.
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- ARTICLES
EKG abnormalities in children and adolescents with symptomatic temporal lobe epilepsy
- H. Mayer, F. Benninger, L. Urak, B. Plattner, J. Geldner, and M. Feucht
Neurology 2004; 63: 324-328.
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- BRIEF COMMUNICATIONS
Neonatal lower motor neuron syndrome associated with maternal neuropathy with anti-GM1 IgG
- S. Attarian, J. -Ph. Azulay, B. Chabrol, N. Escande-Beillard, J. Pouget, and J. Boucraut
Neurology 2004; 63: 379-381.
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- BRIEF COMMUNICATIONS
Detection of novel mutations in the SMN Tudor domain in type I SMA patients
- I. Cuscó, M. Jesus Barceló, E. del Río, M. Baiget, and E. F. Tizzano
Neurology 2004; 63: 146-149.
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- ARTICLES
Dysembryoplastic neuroepithelial tumors in childhood: Long-term outcome and prognostic features
- M. A. Nolan, R. Sakuta, N. Chuang, H. Otsubo, J. T. Rutka, O. C. Snead, III, C. E. Hawkins, and S. K. Weiss
Neurology 2004; 62: 2270-2276.
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- ARTICLES
Anomalous brain activation during face and gaze processing in Williams syndrome
- D. Mobbs, A. S. Garrett, V. Menon, F. E. Rose, U. Bellugi, and A. L. Reiss
Neurology 2004; 62: 2070-2076.
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- BRIEF COMMUNICATIONS
Perinatal stroke in term infants with neonatal encephalopathy
- V. Ramaswamy, S. P. Miller, A. J. Barkovich, J. C. Partridge, and D. M. Ferriero
Neurology 2004; 62: 2088-2091.
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Bilateral generalized polymicrogyria (BGP): A distinct syndrome of cortical malformation
- B. S. Chang, X. Piao, C. Giannini, G. D. Cascino, I. Scheffer, C. G. Woods, M. Topcu, K. Tezcan, A. Bodell, R. J. Leventer, A. J. Barkovich, P. E. Grant, and C. A. Walsh
Neurology 2004; 62: 1722-1728.
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Altered neurometabolite development in HIV-infected children: Correlation with neuropsychological tests
- M. A. Keller, T. N. Venkatraman, A. Thomas, A. Deveikis, C. LoPresti, J. Hayes, N. Berman, I. Walot, S. Padilla, J. Johnston-Jones, T. Ernst, and L. Chang
Neurology 2004; 62: 1810-1817.
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- BRIEF COMMUNICATIONS
Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations
- Vincent Procaccio and Douglas C. Wallace
Neurology 2004; 62: 1899-1901.
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