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All Pediatric
Citations 161-170 of 278 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
Benign alternating hemiplegia of childhood: New features and associations
- Megan Kavanaugh and Gary J. Myers
Neurology 2004; 62: 672.
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- ARTICLES
Muscle weakness in critically ill children
- B. L. Banwell, R. J. Mildner, A. C. Hassall, L. E. Becker, J. Vajsar, and S. D. Shemie
Neurology 2003; 61: 1779-1782.
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- ARTICLES
Atypical cerebral laterality in adults with persistent developmental stuttering
- A. L. Foundas, D. M. Corey, V. Angeles, A. M. Bollich, E. Crabtree–Hartman, and K. M. Heilman
Neurology 2003; 61: 1378-1385.
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- ARTICLES
Neurodevelopmental outcome after endovascular treatment of vein of Galen malformations
- H. J. Fullerton, A. R. Aminoff, D. M. Ferriero, N. Gupta, and C. F. Dowd
Neurology 2003; 61: 1386-1390.
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- EDITORIALS
The brainstem and vulnerability to sudden infant death syndrome
- Bradley T. Thach
Neurology 2003; 61: 1170-1171.
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- BRIEF COMMUNICATIONS
Distinct cytokine profile in SIDS brain: A common denominator in a multifactorial syndrome?
- Hazim Kadhim, André Kahn, and Guillaume Sébire
Neurology 2003; 61: 1256-1259.
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- CLINICAL/SCIENTIFIC NOTES
Contralateral rhinorrhea as a feature of infantile Horner’s syndrome
- J. Takanashi, H. Tada, M. Tomita, K. Fujii, Y. Iida, N. Saeki, and Y. Kohno
Neurology 2003; 61: 1309-1310.
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- ARTICLES
Mosaic mutations of the LIS1 gene cause subcortical band heterotopia
- F. Sicca, A. Kelemen, P. Genton, S. Das, D. Mei, F. Moro, W.B. Dobyns, and R. Guerrini
Neurology 2003; 61: 1042-1046.
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- BRIEF COMMUNICATIONS
SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiency
- A.-R. Moslemi, M. Tulinius, N. Darin, P. Åman, E. Holme, and A. Oldfors
Neurology 2003; 61: 991-993.
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- CLINICAL/SCIENTIFIC NOTES
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit
- V. Petruzzella, G. Di Giacinto, S. Scacco, F. Piemonte, A. Torraco, R. Carrozzo, R. Vergari, C. Dionisi-Vici, D. Longo, A. Tessa, S. Papa, and E. Bertini
Neurology 2003; 61: 1017-1018.
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