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Mental retardation
Citations 1-10 of 32 total displayed.
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Most recent content
(23 Sep 2008):
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- ARTICLES
CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy
- M. Elia, M. Falco, R. Ferri, A. Spalletta, M. Bottitta, G. Calabrese, M. Carotenuto, S. A. Musumeci, M. Lo Giudice, and M. Fichera
Neurology 2008; 71: 997-999.
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Past content
(since Sep 2001):
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- ARTICLES
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome
- J. Nectoux, N. Bahi-Buisson, I. Guellec, J. Coste, N. De Roux, H. Rosas, M. Tardieu, J. Chelly, and T. Bienvenu
Neurology 2008; 70: 2145-2151.
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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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- EDITORIALS
Complicated autosomal recessive hereditary spastic paraplegia: A complex picture is emerging
- Peter Hedera and Oliver Bandmann
Neurology 2008; 70: 1375-1376.
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- ARTICLES
Cognitive impairment in tuberous sclerosis complex is a multifactorial condition
- F. E. Jansen, K. L. Vincken, A. Algra, P. Anbeek, O. Braams, M. Nellist, B. A. Zonnenberg, A. Jennekens-Schinkel, A. van den Ouweland, D. Halley, A. C. van Huffelen, and O. van Nieuwenhuizen
Neurology 2008; 70: 916-923.
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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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- ARTICLES
New POMT2 mutations causing congenital muscular dystrophy: Identification of a founder mutation
- A. Yanagisawa, C. Bouchet, P.Y.K. Van den Bergh, J. -M. Cuisset, L. Viollet, F. Leturcq, N. B. Romero, S. Quijano-Roy, M. Fardeau, N. Seta, and P. Guicheney
Neurology 2007; 69: 1254-1260.
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- EDITORIALS
The ARX story: A new twist
- Cecil D. Hahn
Neurology 2007; 69: 421-422.
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DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation
- H. Engels, A. Brockschmidt, A. Hoischen, C. Landwehr, K. Bosse, C. Walldorf, G. Toedt, B. Radlwimmer, P. Propping, P. Lichter, and R. G. Weber
Neurology 2007; 68: 743-750.
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