Advertisement
Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
 QUICK SEARCH:   [advanced]


     


All Pediatric

Citations 51-60 of 278 total displayed.

Past content (since Jan 2001):

CLINICAL/SCIENTIFIC NOTES
DIAGNOSTIC APPROACHES TO IMPORTED SCHISTOSOMAL MYELORADICULOPATHY IN TRAVELERS
A. Makinson, R. Juntas Morales, D. Basset, O. Bouchaud, R. Verdon, H. Hosseini, V. Le Moing, E. Delaporte, and J. Reynes
Neurology 2008; 71: 66-67. [Full text] [PDF]  

RESIDENT AND FELLOW SECTION
Emerging Subspecialties in Neurology: Building a career and a field: Pediatric neurocritical care
Kerri L. LaRovere and James J. Riviello, Jr
Neurology 2008; 70: e89-91e. [Full text] [PDF]  

EDITORIALS
Still orphans: Antiepileptic drug trials in children under 2 years of age
Howard P. Goodkin and Marcia L. Buck
Neurology 2008; 70: 2093-2094. [Full text] [PDF]  

ARTICLES
Adjunctive lamotrigine for partial seizures in patients aged 1 to 24 months
J. E. Piña-Garza, P. Levisohn, K. Gucuyener, M. A. Mikati, C. R. Warnock, H. S. Conklin, and J. Messenheimer
Neurology 2008; 70: 2099-2108. [Abstract] [Full text] [PDF]  

EDITORIALS
Children get their due: A study of pediatric epilepsy patients before drug approval
W. Donald Shields
Neurology 2008; 70: 1946-1947. [Full text] [PDF]  

ARTICLES
Rufinamide for generalized seizures associated with Lennox–Gastaut syndrome
T. Glauser, G. Kluger, R. Sachdeo, G. Krauss, C. Perdomo, and S. Arroyo
Neurology 2008; 70: 1950-1958. [Abstract] [Full text] [PDF]  

ARTICLES
Endoscopic resection of hypothalamic hamartomas for refractory symptomatic epilepsy
Y. -T. Ng, H. L. Rekate, E. C. Prenger, N. C. Wang, S. S. Chung, I. Feiz-Erfan, R. E. Johnsonbaugh, M. R. Varland, and J. F. Kerrigan
Neurology 2008; 70: 1543-1548. [Abstract] [Full text] [PDF]  

ARTICLES
Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome
J. L. Neul, P. Fang, J. Barrish, J. Lane, E. B. Caeg, E. O. Smith, H. Zoghbi, A. Percy, and D. G. Glaze
Neurology 2008; 70: 1313-1321. [Abstract] [Full text] [PDF]  

ARTICLES
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease
M. Henneke, P. Combes, S. Diekmann, E. Bertini, K. Brockmann, A. P. Burlina, J. Kaiser, A. Ohlenbusch, B. Plecko, D. Rodriguez, O. Boespflug-Tanguy, and J. Gärtner
Neurology 2008; 70: 748-754. [Abstract] [Full text] [PDF]  

EDITORIALS
Epilepsy-associated bone mineral density loss should be prevented
Edwin Trevathan
Neurology 2008; 70: 166-167. [Full text] [PDF]  

[First page]   [Previous page]   [Next page]
Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28

* Collected Resources Home

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


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
Copyright © 2009 by AAN Enterprises, Inc.
Advertisement