Further delineation of the executive deficit in males with fragile-X syndrome

Neuropsychologia

Volumn 40, Issue 8, 2002, Pages 1343-1349

  Wilding, John ^a   Cornish, Kim ^b   Munir, Fehmidah ^b  

^a UNIVERSITY OF LONDON   (United Kingdom)

^b UNIVERSITY OF NOTTINGHAM   (United Kingdom)

Author keywords

Down's syndrome; False alarms; Fragile X syndrome; Inhibition; Response repetition; Response switching

Indexed keywords

ANALYSIS OF VARIANCE; ARTICLE; ATTENTION DEFICIT DISORDER; CLINICAL ARTICLE; CONFUSION; DOWN SYNDROME; ERROR; FEMALE; FRAGILE X SYNDROME; HUMAN; LEARNING DISORDER; MALE; MEMORY; PERFORMANCE; PERSEVERATION; RATING SCALE; SCHOOL CHILD;

EID: 0036131435     PISSN: 00283932     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0028-3932(01)00212-3     Document Type: Article

References (32)

1. Cognitive and behavioural profile of fragile-X boys: correlations to molecular data
2. Early development, temperament, and functional impairment in autism and fragile-X syndrome
3. Specifications of the neurobehavioural associations in males with FX syndrome
4. The nature of the spatial deficit in young females with fragile-X syndrome: a neuropsychological and molecular perspective
5. Spatial cognition in males with fragile-X syndrome: evidence for a neuropsychological phenotype
6. Differential impact of the FMR-1 full mutation on memory and attention functioning: a neuropsychological perspective
7. Variation of the CGG repeat at the fragile-X site results in genetic instability: resolution of the Sherman Paradox
8. Executive functions in young children with autism
9. Fragile-X syndrome
10. Behavioural style of young boys with fragile-X syndrome
11. Early behaviour signs of psychiatric phenotypes in fragile-X syndrome
12. Genotype, molecular phenotype, and cognitive phenotype: correlations in fragile-X syndrome
13. Specific frontal lobe deficits among women with the fragile-X gene
14. Problem solving limitations among cytogenetically expressing fragile-X women
15. The neurocognitive phenotype of female carriers of fragile-X: additional evidence for specificity
16. Molecular-clinical correlations in males with an expanded FMRI mutation
17. Attending, ignoring and repetition: on the relation between negative priming and inhibition of return
18. The unity and diversity of executive functions and their contribution of complex frontal lobe tasks: a latent variable analysis
19. Probing distracter inhibition in visual search: inhibition of return
20. A neuropsychological profile of attention deficits in young males with fragile-X syndrome
21. Executive functions and developmental psychopathology
22. The attention system of the human brain
23. Contribution of the FMRI gene mutation to human intellectual dysfunction
24. Molecular-intelligence correlations in young fragile-X males with a mild CGG repeat expansion in the FMRI gene
25. Fragile-X syndrome and attentional deficits
26. A new rating scale for diagnosis and monitoring of ADD children
27. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile-X syndrome