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Neurology
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Developmental disorders

Citations 41-50 of 105 total displayed.

Past content (since Jan 2001):

VIEWS & REVIEWS
A developmental and genetic classification for malformations of cortical development
A. J. Barkovich, R. I. Kuzniecky, G. D. Jackson, R. Guerrini, and W. B. Dobyns
Neurology 2005; 65: 1873-1887. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Gender differences in handedness and speech lateralization related to early neurologic insults
John W. Miller, Suman Jayadev, Carl B. Dodrill, and George A. Ojemann
Neurology 2005; 65: 1974-1975. [Abstract] [Full text] [PDF]  

ARTICLES
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia
G. Zanni, Y. Saillour, M. Nagara, P. Billuart, L. Castelnau, C. Moraine, L. Faivre, E. Bertini, A. Durr, A. Guichet, D. Rodriguez, V. des Portes, C. Beldjord, and J. Chelly
Neurology 2005; 65: 1364-1369. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
POLG mutations in Alpers syndrome
K. V. Nguyen, E. Østergaard, S. Holst Ravn, T. Balslev, E. Rubæk Danielsen, A. Vardag, P. J. McKiernan, G. Gray, and R. K. Naviaux
Neurology 2005; 65: 1493-1495. [Abstract] [Full text] [PDF]  

EDITORIALS
To sleep, perchance to speak: The search for epileptic language regression
Edwin Trevathan
Neurology 2005; 65: 11-12. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Epileptiform EEG abnormalities in children with language regression
K. A. McVicar, K. Ballaban-Gil, I. Rapin, S. L. Moshé, and S. Shinnar
Neurology 2005; 65: 129-131. [Abstract] [Full text] [PDF]  

ARTICLES
Saccades in children with spina bifida and Chiari type II malformation
M. S. Salman, J. A. Sharpe, M. Eizenman, L. Lillakas, T. To, C. Westall, M. J. Steinbach, and M. Dennis
Neurology 2005; 64: 2098-2101. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett syndrome
J. L. Neul, S. M. Maricich, M. Islam, J. Barrish, E. O’Brian Smith, T. Bottiglieri, K. Hyland, P. Humphreys, A. Percy, and D. Glaze
Neurology 2005; 64: 2151-2152. [Full text] [PDF]  

BRIEF COMMUNICATIONS
The natural history of Aicardi–Goutières syndrome: Follow-up of 11 Italian patients
G. Lanzi, E. Fazzi, S. D’Arrigo, S. Orcesi, I. Maraucci, C. Uggetti, E. Bertini, and P. Lebon
Neurology 2005; 64: 1621-1624. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Evidence for superior parietal impairment in Williams syndrome
M. A. Eckert, D. Hu, S. Eliez, U. Bellugi, A. Galaburda, J. Korenberg, D. Mills, and A. L. Reiss
Neurology 2005; 64: 152-153. [Abstract] [Full text] [PDF]  

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* Related collections:
 Pediatric
 All Pediatric
 Developmental disorders
 Neonatal
 Mental retardation
 Child psychiatry
 Pediatric depression
 Pediatric conversion
 Adolescence
 Autism


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