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Items: 1 to 20 of 75

1.

Fibromyalgia in fragile X mental retardation 1 gene premutation carriers.

Leehey MA, Legg W, Tassone F, Hagerman R.

Rheumatology (Oxford). 2011 Dec;50(12):2233-6. doi: 10.1093/rheumatology/ker273. Epub 2011 Sep 16.

2.

Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in mice.

Hunsaker MR, von Leden RE, Ta BT, Goodrich-Hunsaker NJ, Arque G, Kim K, Willemsen R, Berman RF.

Behav Brain Res. 2011 Sep 12;222(1):117-21. doi: 10.1016/j.bbr.2011.03.039. Epub 2011 Mar 31.

3.

A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis.

Qin M, Entezam A, Usdin K, Huang T, Liu ZH, Hoffman GE, Smith CB.

Neurobiol Dis. 2011 Apr;42(1):85-98. doi: 10.1016/j.nbd.2011.01.008. Epub 2011 Jan 8.

4.

Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers.

Bourgeois JA, Seritan AL, Casillas EM, Hessl D, Schneider A, Yang Y, Kaur I, Cogswell JB, Nguyen DV, Hagerman RJ.

J Clin Psychiatry. 2011 Feb;72(2):175-82. doi: 10.4088/JCP.09m05407blu. Epub 2010 Aug 24.

5.

Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.

Peprah EK, Allen EG, Williams SM, Woodard LM, Sherman SL.

Ann Hum Genet. 2010 Jul;74(4):316-25. doi: 10.1111/j.1469-1809.2010.00582.x.

6.

Parkinsonism and cognitive decline in a fragile X mosaic male.

Hall D, Pickler L, Riley K, Tassone F, Hagerman R.

Mov Disord. 2010 Jul 30;25(10):1523-4. doi: 10.1002/mds.23150. No abstract available.

7.

Involvement of the peripheral nervous system in synucleinopathies, tauopathies and other neurodegenerative proteinopathies of the brain.

Wakabayashi K, Mori F, Tanji K, Orimo S, Takahashi H.

Acta Neuropathol. 2010 Jul;120(1):1-12. doi: 10.1007/s00401-010-0706-x. Epub 2010 Jun 9. Review.

PMID:
20532896
8.

Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome.

Ross-Inta C, Omanska-Klusek A, Wong S, Barrow C, Garcia-Arocena D, Iwahashi C, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Giulivi C.

Biochem J. 2010 Aug 1;429(3):545-52. doi: 10.1042/BJ20091960.

9.

Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation.

Hunsaker MR, Goodrich-Hunsaker NJ, Willemsen R, Berman RF.

Behav Brain Res. 2010 Dec 1;213(2):263-8. doi: 10.1016/j.bbr.2010.05.010. Epub 2010 May 15.

10.

Advances in understanding the molecular basis of FXTAS.

Garcia-Arocena D, Hagerman PJ.

Hum Mol Genet. 2010 Apr 15;19(R1):R83-9. doi: 10.1093/hmg/ddq166. Epub 2010 Apr 29. Review.

11.

Fragile X dementia Parkinsonism Syndrome (FXDPS).

Yachnis AT, Roth HL, Heilman KM.

Cogn Behav Neurol. 2010 Mar;23(1):39-43. doi: 10.1097/WNN.0b013e3181b6e1b9.

PMID:
20299862
12.

Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients.

Sellier C, Rau F, Liu Y, Tassone F, Hukema RK, Gattoni R, Schneider A, Richard S, Willemsen R, Elliott DJ, Hagerman PJ, Charlet-Berguerand N.

EMBO J. 2010 Apr 7;29(7):1248-61. doi: 10.1038/emboj.2010.21. Epub 2010 Feb 25.

13.

Ubiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation.

Wenzel HJ, Hunsaker MR, Greco CM, Willemsen R, Berman RF.

Brain Res. 2010 Mar 8;1318:155-66. doi: 10.1016/j.brainres.2009.12.077. Epub 2010 Jan 4.

14.

Progressive spatial processing deficits in a mouse model of the fragile X premutation.

Hunsaker MR, Wenzel HJ, Willemsen R, Berman RF.

Behav Neurosci. 2009 Dec;123(6):1315-24. doi: 10.1037/a0017616.

15.

Examination of FMR1 transcript and protein levels among 74 premutation carriers.

Peprah E, He W, Allen E, Oliver T, Boyne A, Sherman SL.

J Hum Genet. 2010 Jan;55(1):66-8. doi: 10.1038/jhg.2009.121. Epub 2009 Nov 20.

16.

Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers.

Adams PE, Adams JS, Nguyen DV, Hessl D, Brunberg JA, Tassone F, Zhang W, Koldewyn K, Rivera SM, Grigsby J, Zhang L, Decarli C, Hagerman PJ, Hagerman RJ.

Am J Med Genet B Neuropsychiatr Genet. 2010 Apr 5;153B(3):775-85. doi: 10.1002/ajmg.b.31046.

17.

Fibroblast phenotype in male carriers of FMR1 premutation alleles.

Garcia-Arocena D, Yang JE, Brouwer JR, Tassone F, Iwahashi C, Berry-Kravis EM, Goetz CG, Sumis AM, Zhou L, Nguyen DV, Campos L, Howell E, Ludwig A, Greco C, Willemsen R, Hagerman RJ, Hagerman PJ.

Hum Mol Genet. 2010 Jan 15;19(2):299-312. doi: 10.1093/hmg/ddp497. Epub 2009 Oct 28.

18.

Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration.

Chen Y, Tassone F, Berman RF, Hagerman PJ, Hagerman RJ, Willemsen R, Pessah IN.

Hum Mol Genet. 2010 Jan 1;19(1):196-208. doi: 10.1093/hmg/ddp479.

19.

Molecular pathogenesis of fragile X-associated tremor/ataxia syndrome.

Raske C, Hagerman PJ.

J Investig Med. 2009 Dec;57(8):825-9. doi: 10.2310/JIM.0b013e3181be329a. Review.

20.

Neuropathology of Lewy body disorders.

Kövari E, Horvath J, Bouras C.

Brain Res Bull. 2009 Oct 28;80(4-5):203-10. doi: 10.1016/j.brainresbull.2009.06.018. Epub 2009 Jul 1. Review.

PMID:
19576266

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