Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome

Brain

Volumn 124, Issue 8, 2001, Pages 1610-1618

  Eliez, Stephan ^a   Blasey, Christine M ^a   Freund, Lisa S ^c   Hastie, Trevor ^b   Reiss, Allan L ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b STANFORD UNIVERSITY   (United States)

^c EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

Author keywords

Brain development; FMR1; Fragile X syndrome; MRI

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BRAIN; CEREBROSPINAL FLUID ANALYSIS; CHILD; CLINICAL ARTICLE; COGNITION; CORRELATION FUNCTION; DEVELOPMENTAL DISORDER; FEMALE; FRAGILE X SYNDROME; GENDER; GRAY MATTER; HANDICAPPED CHILD; HUMAN; INTELLIGENCE QUOTIENT; MALE; NEUROANATOMY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; STATISTICAL ANALYSIS;

EID: 0034896495     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/124.8.1610     Document Type: Article

References (53)

1. Intelligence and brain structure in normal individuals
2. Specification of the neurobehavioral phenotype in males with fragile X syndrome
3. Improvement of Kittler and Illingworth's minimum error thresholding
4. Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits
5. Neuropsychological dimensions of the fragile X syndrome: Support for a non-dominant hemisphere dysfunction hypothesis
6. Orthopaedic aspects of fragile-X syndrome
7. Screening and diagnosis for the fragile X syndrome among the mentally retarded: An epidemiological and psychological survey
8. The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation
9. Behavioural and emotional disturbance in fragile X syndrome
10. Autism: The point of view from fragile X studies
11. Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes
12. Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis
13. Psychiatric disorders associated with fragile X in the young female
14. Quantitative magnetic resonance imaging of human brain development: Ages 4-18
15. Brain development during childhood and adolescence: A longitudinal MRI study
16. Fragile X syndrome. Clinical, electroencephalographic and neuroimaging characteristics
17. Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county
18. Analysis of neocortex in three males with the fragile X syndrome
19. Developmental implications of changing trajectories of IQ in males with fragile X syndrome
20. Individual variation of cortical surface area asymmetries
21. Fragile-X: Neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes
22. Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome
23. Cognitive profiles of boys with the fragile X syndrome
24. How can we learn about developmental processes from cross-sectional studies, or can we?
25. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
26. Do young boys with fragile X syndrome have macroorchidism?
27. Aberrant behaviors of young boys with fragile X syndrome
28. Clinical features and reproductive patterns in fragile X female heterozygotes
29. A marker X chromosome
30. Brief report: Autistic behaviors among children with fragile X or Rett syndrome: Implications for the classification of pervasive developmental disorder
31. An anthropometric study of males with the fragile-X syndrome
32. Decreased cerebellar posterior vermis size in fragile X syndrome: Correlation with neurocognitive performance
33. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
34. A treshold selection method from gray-level histograms
35. A quantitative magnetic resonance imaging study of changes in brain morphology from infancy to late adulthood
36. Neuroanatomy of fragile X syndrome: The temporal lobe
37. Neurodevelopmental effects of the FMR-1 full mutation in humans
38. Brain development, gender and IQ in children. A volumetric imaging study
39. Phenotypic involvement in females with the FMR1 gene mutation
40. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation
41. Adult fragile X syndrome. Clinico-neuropathologic findings
42. Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis
43. The fragile-X syndrome. On the way to a behavioural phenotype
44. Face recognition and emotion perception in boys with fragile-X syndrome
45. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
46. Statistical methods for summarizing independent correlational results
47. Triplet repeat expansion mutations: The example of fragile X syndrome
48. Synaptic synthesis of the fragile X protein: Possible involvement in synapse maturation and elimination
49. The Fra(X) syndrome: Neurological, electrophysiological, and neuropathological abnormalities
50. Women have greater density of neurons in posterior temporal cortex
51. A controlled study of longitudinal IQ changes in females and males with fragile X syndrome