335 related articles for article (PubMed ID: 17932962)
1. Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP).
Gothelf D; Furfaro JA; Hoeft F; Eckert MA; Hall SS; O'Hara R; Erba HW; Ringel J; Hayashi KM; Patnaik S; Golianu B; Kraemer HC; Thompson PM; Piven J; Reiss AL
Ann Neurol; 2008 Jan; 63(1):40-51. PubMed ID: 17932962
[TBL] [Abstract][Full Text] [Related]
2. Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS).
Adams JS; Adams PE; Nguyen D; Brunberg JA; Tassone F; Zhang W; Koldewyn K; Rivera SM; Grigsby J; Zhang L; DeCarli C; Hagerman PJ; Hagerman RJ
Neurology; 2007 Aug; 69(9):851-9. PubMed ID: 17724287
[TBL] [Abstract][Full Text] [Related]
3. Functional neuroanatomy of visuospatial working memory in fragile X syndrome: relation to behavioral and molecular measures.
Kwon H; Menon V; Eliez S; Warsofsky IS; White CD; Dyer-Friedman J; Taylor AK; Glover GH; Reiss AL
Am J Psychiatry; 2001 Jul; 158(7):1040-51. PubMed ID: 11431225
[TBL] [Abstract][Full Text] [Related]
4. A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndrome.
Hashimoto R; Javan AK; Tassone F; Hagerman RJ; Rivera SM
Brain; 2011 Mar; 134(Pt 3):863-78. PubMed ID: 21354978
[TBL] [Abstract][Full Text] [Related]
5. The behavioral neurogenetics of fragile X syndrome: analyzing gene-brain-behavior relationships in child developmental psychopathologies.
Reiss AL; Dant CC
Dev Psychopathol; 2003; 15(4):927-68. PubMed ID: 14984133
[TBL] [Abstract][Full Text] [Related]
6. Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction.
Brunberg JA; Jacquemont S; Hagerman RJ; Berry-Kravis EM; Grigsby J; Leehey MA; Tassone F; Brown WT; Greco CM; Hagerman PJ
AJNR Am J Neuroradiol; 2002; 23(10):1757-66. PubMed ID: 12427636
[TBL] [Abstract][Full Text] [Related]
7. [Fragile X syndrome and white matter abnormalities: Case study of two brothers].
Wallach E; Bieth E; Sevely A; Cances C
Arch Pediatr; 2017 Mar; 24(3):244-248. PubMed ID: 28131561
[TBL] [Abstract][Full Text] [Related]
8. Quantitative measurement of FMRP in blood platelets as a new screening test for fragile X syndrome.
Lessard M; Chouiali A; Drouin R; Sébire G; Corbin F
Clin Genet; 2012 Nov; 82(5):472-7. PubMed ID: 21992468
[TBL] [Abstract][Full Text] [Related]
9. Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation.
Hessl D; Wang JM; Schneider A; Koldewyn K; Le L; Iwahashi C; Cheung K; Tassone F; Hagerman PJ; Rivera SM
Biol Psychiatry; 2011 Nov; 70(9):859-65. PubMed ID: 21783174
[TBL] [Abstract][Full Text] [Related]
10. Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome.
Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL
Brain; 2001 Aug; 124(Pt 8):1610-8. PubMed ID: 11459752
[TBL] [Abstract][Full Text] [Related]
11. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
Taylor AK; Safanda JF; Fall MZ; Quince C; Lang KA; Hull CE; Carpenter I; Staley LW; Hagerman RJ
JAMA; 1994 Feb; 271(7):507-14. PubMed ID: 8301764
[TBL] [Abstract][Full Text] [Related]
12. FMR1 gene mutations cause neurodevelopmental-degenerative disorders: Importance of fragile X testing in Serbia.
Budimirovic DB; Protic D
Vojnosanit Pregl; 2016 Dec; 73(12):1089-93. PubMed ID: 29341564
[No Abstract] [Full Text] [Related]
13. FMRP Expression Levels in Mouse Central Nervous System Neurons Determine Behavioral Phenotype.
Arsenault J; Gholizadeh S; Niibori Y; Pacey LK; Halder SK; Koxhioni E; Konno A; Hirai H; Hampson DR
Hum Gene Ther; 2016 Dec; 27(12):982-996. PubMed ID: 27604541
[TBL] [Abstract][Full Text] [Related]
14. Effects of a social stimulus on gene expression in a mouse model of fragile X syndrome.
Rogers TD; Anacker AMJ; Kerr TM; Forsberg CG; Wang J; Zhang B; Veenstra-VanderWeele J
Mol Autism; 2017; 8():30. PubMed ID: 28649315
[TBL] [Abstract][Full Text] [Related]
15. Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
Sheridan SD; Theriault KM; Reis SA; Zhou F; Madison JM; Daheron L; Loring JF; Haggarty SJ
PLoS One; 2011; 6(10):e26203. PubMed ID: 22022567
[TBL] [Abstract][Full Text] [Related]
16. Volumetric neuroimaging in children with neurodevelopmental disorders--mapping the brain and behavior.
Chang YC; Huang CC; Huang SC
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1998; 39(5):285-92. PubMed ID: 9823671
[TBL] [Abstract][Full Text] [Related]
17. Fear-specific amygdala function in children and adolescents on the fragile x spectrum: a dosage response of the FMR1 gene.
Kim SY; Burris J; Bassal F; Koldewyn K; Chattarji S; Tassone F; Hessl D; Rivera SM
Cereb Cortex; 2014 Mar; 24(3):600-13. PubMed ID: 23146966
[TBL] [Abstract][Full Text] [Related]
18. Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 gene.
Govaerts LC; Smit AE; Saris JJ; VanderWerf F; Willemsen R; Bakker CE; De Zeeuw CI; Oostra BA
Clin Genet; 2007 Aug; 72(2):138-44. PubMed ID: 17661818
[TBL] [Abstract][Full Text] [Related]
19. Newborn, carrier, and early childhood screening recommendations for fragile X.
Abrams L; Cronister A; Brown WT; Tassone F; Sherman SL; Finucane B; McConkie-Rosell A; Hagerman R; Kaufmann WE; Picker J; Coffey S; Skinner D; Johnson V; Miller R; Berry-Kravis E
Pediatrics; 2012 Dec; 130(6):1126-35. PubMed ID: 23129072
[TBL] [Abstract][Full Text] [Related]
20. Atypical clinical course of FXTAS: rapidly progressive dementia as the major symptom.
Gonçalves MR; Capelli LP; Nitrini R; Barbosa ER; Porto CS; Lucato LT; Vianna-Morgante AM
Neurology; 2007 May; 68(21):1864-6. PubMed ID: 17515552
[No Abstract] [Full Text] [Related]
[Next] [New Search]