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All Pediatric
Citations 151-160 of 280 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly
- U. Aguglia, A. Gambardella, G. J. Breedveld, R. L. Oliveri, E. Le Piane, D. Messina, A. Quattrone, and P. Heutink
Neurology 2004; 62: 1613-1615.
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- ARTICLES
Long-term sequelae in children after cerebellar astrocytoma surgery
- F. K. Aarsen, H. R. Van Dongen, P. F. Paquier, M. Van Mourik, and C. E. Catsman-Berrevoets
Neurology 2004; 62: 1311-1316.
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- VIEWS & REVIEWS
Aromatic L-amino acid decarboxylase deficiency: Clinical features, treatment, and prognosis
- R. Pons, B. Ford, C. A. Chiriboga, P. T. Clayton, V. Hinton, K. Hyland, R. Sharma, and D. C. De Vivo
Neurology 2004; 62: 1058-1065.
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- BRIEF COMMUNICATIONS
Leukoencephalopathy, cerebral calcifications, and cysts: New observations
- L. M. Nagae-Poetscher, G. Bibat, M. Philippart, S. Rosemberg, A. Fatemi, M. T.C. Lacerda, M. O.R. Costa, F. Kok, C. Costa Leite, A. Horská, P. B. Barker, and S. Naidu
Neurology 2004; 62: 1206-1209.
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- EDITORIALS
Pediatric neurology’s midlife crisis
- Steven M. Rothman
Neurology 2004; 62: 845-846.
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- SPECIAL ARTICLES
Practice Parameter: Diagnostic assessment of the child with cerebral palsy: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
- S. Ashwal, B. S. Russman, P. A. Blasco, G. Miller, A. Sandler, M. Shevell, and R. Stevenson
Neurology 2004; 62: 851-863.
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- CONTEMPORARY ISSUES
State of training in child neurology 1997–2002
- E. Laureta and S.L. Moshé
Neurology 2004; 62: 864-869.
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- VIEWS & REVIEWS
Cognitive side effects of antiepileptic drugs in children
- David W. Loring and Kimford J. Meador
Neurology 2004; 62: 872-877.
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- ARTICLES
Indian Agarwal megalencephalic leukodystrophy with cysts is caused by a common MLC1 mutation
- J. R. Gorospe, B. S. Singhal, T. Kainu, F. Wu, D. Stephan, J. Trent, E. P. Hoffman, and S. Naidu
Neurology 2004; 62: 878-882.
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- BRIEF COMMUNICATIONS
Mevalonate kinase deficiency: Evidence for a phenotypic continuum
- A. Simon, H. P.H. Kremer, R. A. Wevers, H. Scheffer, J. G. de Jong, J. W.M. van der Meer, and J. P.H. Drenth
Neurology 2004; 62: 994-997.
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