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All Pediatric
Citations 1-10 of 240 total displayed.
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Most recent content
(2 Dec 2008):
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- RESIDENT AND FELLOW SECTION
Child Neurology: Chronic inflammatory demyelinating polyradiculoneuropathy in children
- Jennifer A. Markowitz, Shafali S. Jeste, and Peter B. Kang
Neurology 2008; 71: e74-78e.
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Past content
(since Jan 2001):
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- ARTICLES
Diffusion tensor imaging of the pyramidal tracts in infants with motor dysfunction
- N. A. Ludeman, J. I. Berman, Y. W. Wu, R. J. Jeremy, J. Kornak, A. I. Bartha, A. J. Barkovich, D. M. Ferriero, R. G. Henry, and O. A. Glenn
Neurology 2008; 71: 1676-1682.
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- ARTICLES
Neurodegeneration associated with genetic defects in phospholipase A2
- A. Gregory, S. K. Westaway, I. E. Holm, P. T. Kotzbauer, P. Hogarth, S. Sonek, J. C. Coryell, T. M. Nguyen, N. Nardocci, G. Zorzi, D. Rodriguez, I. Desguerre, E. Bertini, A. Simonati, B. Levinson, C. Dias, C. Barbot, I. Carrilho, M. Santos, I. Malik, J. Gitschier, and S. J. Hayflick
Neurology 2008; 71: 1402-1409.
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- RESIDENT AND FELLOW SECTION
Teaching Video NeuroImage: Near complete ophthalmoplegia in GQ1b antibody-positive Miller Fisher: Video and MRI correlation
- David T. Hsieh, Rani Singh, Nassim Zecavati, and Ben Emmanuel
Neurology 2008; 71: e31.
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- ARTICLES
Vanishing MS T2-bright lesions before puberty: A distinct MRI phenotype?
- D. Chabas, T. Castillo-Trivino, E. M. Mowry, J. B. Strober, O. A. Glenn, and E. Waubant
Neurology 2008; 71: 1090-1093.
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- ARTICLES
Prognostic factors after a first attack of inflammatory CNS demyelination in children
- R. F. Neuteboom, M. Boon, C. E. Catsman Berrevoets, J. S. Vles, R. H. Gooskens, H. Stroink, R. J. Vermeulen, J. J. Rotteveel, I. A. Ketelslegers, E. Peeters, B. T. Poll-The, J. F. De Rijk-Van Andel, A. Verrips, and R. Q. Hintzen
Neurology 2008; 71: 967-973.
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- CLINICAL/SCIENTIFIC NOTES
TWO SETS OF IDENTICAL TWINS WITH CERVICAL ARTERY DISSECTION CONCORDANT FOR TEMPORAL ARTERY PATHOLOGY
- W. Völker, G. Kuhlenbäumer, R. Dittrich, S. Appenzeller, S. Grewe, D. Maintz, W. Heindel, K. H. Grotemeyer, and E. B. Ringelstein
Neurology 2008; 71: 1035-1037.
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- CLINICAL/SCIENTIFIC NOTES
KING-DENBOROUGH SYNDROME CAUSED BY A NOVEL MUTATION IN THE RYANODINE RECEPTOR GENE
- C. E. DArcy, A. Bjorksten, E. M. Yiu, A. Bankier, R. Gillies, C. A. McLean, L. K. Shield, and M. M. Ryan
Neurology 2008; 71: 776-777.
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- ARTICLES
Presyrinx in children with Chiari malformations
- S. Goh, C. L. Bottrell, A. H. Aiken, W. P. Dillon, and Y. W. Wu
Neurology 2008; 71: 351-356.
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- EDITORIALS
Prolonged febrile seizures: Underrecognized and perhaps underappreciated?
- Gregory L. Holmes and Marc A. Dichter
Neurology 2008; 71: 162-163.
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