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Developmental disorders
Citations 1-10 of 104 total displayed.
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Most recent content
(15 Sep 2009):
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- SPECIAL ARTICLE
Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
- Stephen Ashwal, David Michelson, Lauren Plawner, and William B. Dobyns
Neurology 2009; 73: 887-897.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
FAMILIAL CONGENITAL MIRROR MOVEMENTS: REPORT OF A LARGE 4-GENERATION FAMILY
- M. Srour, M. Philibert, M. -H. Dion, A. Duquette, F. Richer, G. A. Rouleau, and S. Chouinard
Neurology 2009; 73: 729-731.
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- RESIDENT AND FELLOW SECTION
Child Neurology: Autism as a model: Considerations for advanced training in behavioral child neurology
- Shafali S. Jeste, Sandra L. Friedman, and David K. Urion
Neurology 2009; 73: 733-735.
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- ARTICLES
Comorbidities in cerebral palsy and their relationship to neurologic subtype and GMFCS level
- Michael I. Shevell, Lynn Dagenais, Nicholas Hall On behalf of the REPACQ Consortium
Neurology 2009; 72: 2090-2096.
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- ARTICLES
Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia
- M. Carbon, M. Niethammer, S. Peng, D. Raymond, V. Dhawan, T. Chaly, Y. Ma, S. Bressman, and D. Eidelberg
Neurology 2009; 72: 2097-2103.
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- ARTICLES
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
- B. Ben Zeev, A. Bebbington, G. Ho, H. Leonard, N. de Klerk, E. Gak, M. Vecksler, and J. Christodoulou
Neurology 2009; 72: 1242-1247.
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- EDITORIALS
Cortical malformations: Looking behind the cortex
- Harvey B. Sarnat
Neurology 2009; 72: 394-395.
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- EDITORIALS
Epilepsy surgery patients with cortical dysplasia: Present and future therapeutic challenges
- Gary W. Mathern
Neurology 2009; 72: 206-207.
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- ARTICLES
Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1
- D. S. Stamm, C. M. Powell, J. M. Stajich, V. L. Zismann, D. A. Stephan, B. Chesnut, A. S. Aylsworth, S. G. Kahler, K. L. Deak, J. R. Gilbert, and M. C. Speer
Neurology 2008; 71: 1764-1769.
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- ARTICLES
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debré type
- L. Van Maldergem, M. Yuksel-Apak, H. Kayserili, E. Seemanova, S. Giurgea, L. Basel-Vanagaite, E. Leao-Teles, J. Vigneron, M. Foulon, M. Greally, J. Jaeken, S. Mundlos, and W. B. Dobyns
Neurology 2008; 71: 1602-1608.
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