|
Developmental disorders
Citations 21-30 of 105 total displayed.
|
Past content
(since Jan 2001):
|
- VIEWS & REVIEWS
The molar tooth sign: A new Joubert syndrome and related cerebellar disorders classification system tested in Egyptian families
- M. S. Zaki, A. Abdel-Aleem, G. Abdel-Salam, S. E. Marsh, J. L. Silhavy, A. J. Barkovich, M. E. Ross, S. N. Saleem, W. B. Dobyns, and J. G. Gleeson
Neurology 2008; 70: 556-565.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
PHANTOM ARM AND LEG AFTER PONTINE HEMORRHAGE
- H. Tanaka, M. Arai, T. Kadowaki, H. Takekawa, N. Kokubun, and K. Hirata
Neurology 2008; 70: 82-83.
[Full text]
[PDF]
- ARTICLES
A structural basis for reading fluency: White matter defects in a genetic brain malformation
- B. S. Chang, T. Katzir, T. Liu, K. Corriveau, M. Barzillai, K. A. Apse, A. Bodell, D. Hackney, D. Alsop, S. Wong, and C. A. Walsh
Neurology 2007; 69: 2146-2154.
[Abstract]
[Full text]
[PDF]
- EDITORIALS
Smooth mosaics: Genotype and phenotype in lissencephaly
- Hans H. Jung
Neurology 2007; 69: 425-426.
[Full text]
[PDF]
- ARTICLES
Location and type of mutation in the LIS1 gene do not predict phenotypic severity
- G. Uyanik, D. J. Morris-Rosendahl, J. Stiegler, J. Klapecki, C. Gross, Y. Berman, P. Martin, L. Dey, S. Spranger, G. C. Korenke, I. Schreyer, C. Hertzberg, T. E. Neumann, P. Burkart, C. Spaich, M. Meng, H. Holthausen, L. Adès, J. Seidel, E. Mangold, G. Buyse, P. Meinecke, U. Schara, C. Zeschnigk, D. Muller, G. Helland, B. Schulze, M. L. Wright, S. Kortge-Jung, A. Hehr, U. Bogdahn, G. Schuierer, J. Kohlhase, L. Aigner, G. Wolff, U. Hehr, and J. Winkler
Neurology 2007; 69: 442-447.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
MONOZYGOTIC TWINS WITH MIRROR IMAGE CYSTS: INDICATION OF A GENETIC MECHANISM IN ARACHNOID CYSTS?
- Christian A. Helland and Knut Wester
Neurology 2007; 69: 110-111.
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
NEUROLOGICAL FINDINGS IN AMINOACYLASE 1 DEFICIENCY
- J. O. Sass, H. Olbrich, V. Mohr, C. Hart, B. Woldseth, S. Krywawych, B. Bjurulf, P. K. Lakhani, R. M. Buchdahl, and H. Omran
Neurology 2007; 68: 2151-2153.
[Full text]
[PDF]
- ARTICLES
Infantile spasm–associated microencephaly in tuberous sclerosis complex and cortical dysplasia
- P. S. Chandra, N. Salamon, S. T. Nguyen, J. W. Chang, M. N. Huynh, C. Cepeda, J. P. Leite, L. Neder, S. Koh, H. V. Vinters, and G. W. Mathern
Neurology 2007; 68: 438-445.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Abnormal orbitofrontal development due to prematurity
- M. Giménez, C. Junqué, P. Vendrell, A. Narberhaus, N. Bargalló, F. Botet, and J. M. Mercader
Neurology 2006; 67: 1818-1822.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Absence of cognitive, behavioral, or emotional dysfunction in progressive muscular atrophy
- P. Wicks, S. Abrahams, P. N. Leigh, T. Williams, and L. H. Goldstein
Neurology 2006; 67: 1718-1719.
[Full text]
[PDF]
|
|
