|
Mental retardation
Citations 11-20 of 34 total displayed.
|
Past content
(since Sep 2001):
|
- EDITORIALS
The ARX story: A new twist
- Cecil D. Hahn
Neurology 2007; 69: 421-422.
[Full text]
[PDF]
- ARTICLES
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.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Multiplex ligation-dependent probe amplification detects DCX gene deletions in band heterotopia
- D. Mei, E. Parrini, M. Pasqualetti, G. Tortorella, E. Franzoni, U. Giussani, C. Marini, S. Migliarini, and R. Guerrini
Neurology 2007; 68: 446-450.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Genotype-phenotype associations for ARX gene duplication in X-linked mental retardation
- K. Szczaluba, M. Nawara, K. Poirier, J. Pilch, M. Gajdulewicz, K. Spodar, J. Chelly, J. Bal, and T. Mazurczak
Neurology 2006; 67: 2073-2075.
[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]
- ARTICLES
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia
- G. Zanni, Y. Saillour, M. Nagara, P. Billuart, L. Castelnau, C. Moraine, L. Faivre, E. Bertini, A. Durr, A. Guichet, D. Rodriguez, V. des Portes, C. Beldjord, and J. Chelly
Neurology 2005; 65: 1364-1369.
[Abstract]
[Full text]
[PDF]
- ARTICLES
The nature and frequency of cognitive deficits in children with neurofibromatosis type 1
- Shelley L. Hyman, Arthur Shores, and Kathryn N. North
Neurology 2005; 65: 1037-1044.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Evidence for superior parietal impairment in Williams syndrome
- M. A. Eckert, D. Hu, S. Eliez, U. Bellugi, A. Galaburda, J. Korenberg, D. Mills, and A. L. Reiss
Neurology 2005; 64: 152-153.
[Abstract]
[Full text]
[PDF]
- ARTICLES
The predictive value of a preschool diagnosis of developmental language impairment
- Richard I. Webster, Annette Majnemer, Robert W. Platt, and Michael I. Shevell
Neurology 2004; 63: 2327-2331.
[Abstract]
[Full text]
[PDF]
- ARTICLES
A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation
- Joseph J. Higgins, Joanna Pucilowska, Roni Q. Lombardi, and John P. Rooney
Neurology 2004; 63: 1927-1931.
[Abstract]
[Full text]
[PDF]
|
|
