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Developmental disorders
Citations 1-10 of 88 total displayed.
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Most recent content
(8 Jul 2008):
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- ARTICLES
Two-year placebo-controlled trial of botulinum toxin A for leg spasticity in cerebral palsy
- A. P. Moore, R. A. Ade-Hall, C. Tudu Smith, L. Rosenbloom, H.P.J. Walsh, K. Mohamed, and P. R. Williamson
Neurology 2008; 71: 122-128.
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Past content
(since Jan 2001):
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- 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.
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- ARTICLES
Investigating genotype–phenotype relationships in Rett syndrome using an international data set
- A. Bebbington, A. Anderson, D. Ravine, S. Fyfe, M. Pineda, N. de Klerk, B. Ben-Zeev, N. Yatawara, A. Percy, W. E. Kaufmann, and H. Leonard
Neurology 2008; 70: 868-875.
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- 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.
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- 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.
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- 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.
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- EDITORIALS
Smooth mosaics: Genotype and phenotype in lissencephaly
- Hans H. Jung
Neurology 2007; 69: 425-426.
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- 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.
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- 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.
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- 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.
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