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All Pediatric
Citations 231-240 of 278 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Diffusion tensor imaging of periventricular leukomalacia shows affected sensory cortex white matter pathways
- A. H. Hoon, Jr., W. T. Lawrie, Jr., E. R. Melhem, E. M. Reinhardt, P. C.M. van Zijl, M. Solaiyappan, H. Jiang, M. V. Johnston, and S. Mori
Neurology 2002; 59: 752-756.
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- CLINICAL/SCIENTIFIC NOTES
Adverse effects of phenytoin given for late-onset seizures in adults with Down syndrome
- John A. Tsiouris, Paul J. Patti, Omer Tipu, and Simhachalam Raguthu
Neurology 2002; 59: 779-780.
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- SPECIAL ARTICLES
Practice parameter: Evaluation of children and adolescents with recurrent headaches: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
- D. W. Lewis, S. Ashwal, G. Dahl, D. Dorbad, D. Hirtz, A. Prensky, and I. Jarjour
Neurology 2002; 59: 490-498.
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- BRIEF COMMUNICATIONS
Valproate embryopathy in three sets of siblings: Further proof of hereditary susceptibility
- H. Malm, E. Kajantie, S. Kivirikko, H. Kääriäinen, M. Peippo, and M. Somer
Neurology 2002; 59: 630-633.
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- CLINICAL/SCIENTIFIC NOTES
Abnormal cortical development shown by 3D MRI in Prader–Willi syndrome
- Akira Yoshii, Kalpathy S. Krishnamoorthy, and P. Ellen Grant
Neurology 2002; 59: 644.
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- VIEWS & REVIEWS
The neurogenetics of mucolipidosis type IV
- G. Altarescu, M. Sun, D. F. Moore, J. A. Smith, E. A. Wiggs, B. I. Solomon, N. J. Patronas, K. P. Frei, S. Gupta, C. R. Kaneski, O. W. Quarrell, S. A. Slaugenhaupt, E. Goldin, and R. Schiffmann
Neurology 2002; 59: 306-313.
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- BRIEF COMMUNICATIONS
Multiple risk factors in neonatal sinovenous thrombosis
- Y. W. Wu, S. P. Miller, K. Chin, A. E. Collins, S. C. Lomeli, N. A. Chuang, A. J. Barkovich, and D. M. Ferriero
Neurology 2002; 59: 438-440.
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- ARTICLES
Developmental language disorder associated with polymicrogyria
- M. M. Guerreiro, S. R.V. Hage, C. A. Guimarães, D. V. Abramides, W. Fernandes, P. S. Pacheco, A. M.S.G. Piovesana, M. A. Montenegro, and F. Cendes
Neurology 2002; 59: 245-250.
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- BRIEF COMMUNICATIONS
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores
- H. Jungbluth, C. R. Müller, B. Halliger–Keller, M. Brockington, S. C. Brown, L. Feng, A. Chattopadhyay, E. Mercuri, A. Y. Manzur, A. Ferreiro, N. G. Laing, M. R. Davis, H. P. Roper, V. Dubowitz, G. Bydder, C. A. Sewry, and F. Muntoni
Neurology 2002; 59: 284-287.
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- EDITORIALS
Neurocognitive sequelae of cancer treatment
- Roger J. Packer and Minesh Mehta
Neurology 2002; 59: 8-10.
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