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All Pediatric
Citations 181-190 of 278 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Dysplasia: A common finding in intractable pediatric temporal lobe epilepsy
- B. E. Porter, A. R. Judkins, R. R. Clancy, A. Duhaime, D. J. Dlugos, and J. A. Golden
Neurology 2003; 61: 365-368.
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- BRIEF COMMUNICATIONS
A neonatal form of glycogen storage disease type IV
- M. Nambu, K. Kawabe, T. Fukuda, T. B. Okuno, S. Ohta, I. Nonaka, H. Sugie, and I. Nishino
Neurology 2003; 61: 392-394.
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- BRIEF COMMUNICATIONS
Prolonged treatment for acute symptomatic refractory status epilepticus: Outcome in children
- Mustafa Sahin, Caroline C. Menache, Gregory L. Holmes, and James J. Riviello, Jr.
Neurology 2003; 61: 398-401.
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- EDITORIALS
Mental retardation: X marks the spot
- Marc C. Patterson and Huda Y. Zoghbi
Neurology 2003; 61: 156-157.
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- ARTICLES
Instructional treatment associated with changes in brain activation in children with dyslexia
- E.H. Aylward, T.L. Richards, V.W. Berninger, W.E. Nagy, K.M. Field, A.C. Grimme, A.L. Richards, J.B. Thomson, and S.C. Cramer
Neurology 2003; 61: 212-219.
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- ARTICLES
Autosomal dominant acute necrotizing encephalopathy
- D. E. Neilson, R. M. Eiben, S. Waniewski, C. L. Hoppel, M. E. Varnes, B. A. Bangert, M. Wiznitzer, M. L. Warman, and D. S. Kerr
Neurology 2003; 61: 226-230.
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- BRIEF COMMUNICATIONS
ARX mutations in X-linked lissencephaly with abnormal genitalia
- G. Uyanik, L. Aigner, P. Martin, C. Groß, D. Neumann, H. Marschner-Schäfer, U. Hehr, and J. Winkler
Neurology 2003; 61: 232-235.
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- BRIEF COMMUNICATIONS
Herpes simplex encephalitis relapses in children: Differentiation of two neurologic entities
- X. De Tiège, F. Rozenberg, V. Des Portes, J.B. Lobut, P. Lebon, G. Ponsot, and B. Héron
Neurology 2003; 61: 241-243.
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- CLINICAL/SCIENTIFIC NOTES
Polyalanine expansion of ARX associated with cryptogenic West syndrome
- M. Kato, S. Das, K. Petras, Y. Sawaishi, and W.B. Dobyns
Neurology 2003; 61: 267-276.
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- CLINICAL/SCIENTIFIC NOTES
Serum prolactin in symptomatic and asymptomatic dopa-responsive dystonia due to a GCH1 mutation
- Y. Furukawa, M. Guttman, H. Wong, S.A. Farrell, S. Furtado, and S.J. Kish
Neurology 2003; 61: 269-270.
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