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Mental retardation
Citations 1-10 of 34 total displayed.
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Most recent content
(15 Sep 2009):
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- SPECIAL ARTICLE
Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
- Stephen Ashwal, David Michelson, Lauren Plawner, and William B. Dobyns
Neurology 2009; 73: 887-897.
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Past content
(since Sep 2001):
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- ARTICLES
Decreased GABA-A binding on FMZ-PET in succinic semialdehyde dehydrogenase deficiency
- P. L. Pearl, K. M. Gibson, Z. Quezado, I. Dustin, J. Taylor, S. Trzcinski, J. Schreiber, K. Forester, P. Reeves-Tyer, C. Liew, S. Shamim, P. Herscovitch, R. Carson, J. Butman, C. Jakobs, and W. Theodore
Neurology 2009; 73: 423-429.
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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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- 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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