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Items: 1 to 20 of 548

1.

Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.

Wang JY, Hessl D, Schneider A, Tassone F, Hagerman RJ, Rivera SM.

JAMA Neurol. 2013 Aug;70(8):1022-9. doi: 10.1001/jamaneurol.2013.2934.

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 28;69(9):851-9.

PMID:
17724287
3.

Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males.

Birch RC, Hocking DR, Cornish KM, Menant JC, Georgiou-Karistianis N, Godler DE, Wen W, Hackett A, Rogers C, Trollor JN.

Genes Brain Behav. 2015 Mar;14(3):251-9. doi: 10.1111/gbb.12204. Epub 2015 Mar 25.

PMID:
25689687
4.

Diffusion tensor imaging in male premutation carriers of the fragile X mental retardation gene.

Hashimoto R, Srivastava S, Tassone F, Hagerman RJ, Rivera SM.

Mov Disord. 2011 Jun;26(7):1329-36. doi: 10.1002/mds.23646. Epub 2011 Apr 11.

5.

Unstable mutations in the FMR1 gene and the phenotypes.

Loesch D, Hagerman R.

Adv Exp Med Biol. 2012;769:78-114. Review.

6.

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.

Jacquemont S, Hagerman RJ, Leehey MA, Hall DA, Levine RA, Brunberg JA, Zhang L, Jardini T, Gane LW, Harris SW, Herman K, Grigsby J, Greco CM, Berry-Kravis E, Tassone F, Hagerman PJ.

JAMA. 2004 Jan 28;291(4):460-9.

PMID:
14747503
7.
8.

Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).

Greco CM, Berman RF, Martin RM, Tassone F, Schwartz PH, Chang A, Trapp BD, Iwahashi C, Brunberg J, Grigsby J, Hessl D, Becker EJ, Papazian J, Leehey MA, Hagerman RJ, Hagerman PJ.

Brain. 2006 Jan;129(Pt 1):243-55. Epub 2005 Dec 5.

9.

Age-dependent structural connectivity effects in fragile x premutation.

Wang JY, Hessl DH, Hagerman RJ, Tassone F, Rivera SM.

Arch Neurol. 2012 Apr;69(4):482-9. doi: 10.1001/archneurol.2011.2023.

10.

Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriers.

Liu Y, Winarni TI, Zhang L, Tassone F, Hagerman RJ.

Clin Genet. 2013 Jul;84(1):74-7. doi: 10.1111/cge.12026. Epub 2012 Oct 17.

PMID:
23009394
11.

FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.

Leehey MA, Berry-Kravis E, Goetz CG, Zhang L, Hall DA, Li L, Rice CD, Lara R, Cogswell J, Reynolds A, Gane L, Jacquemont S, Tassone F, Grigsby J, Hagerman RJ, Hagerman PJ.

Neurology. 2008 Apr 15;70(16 Pt 2):1397-402. Epub 2007 Dec 5.

12.

White matter disease and cognitive impairment in FMR1 premutation carriers.

Filley CM, Brown MS, Onderko K, Ray M, Bennett RE, Berry-Kravis E, Grigsby J.

Neurology. 2015 May 26;84(21):2146-52. doi: 10.1212/WNL.0000000000001612. Epub 2015 Apr 29.

13.

Size bias of fragile X premutation alleles in late-onset movement disorders.

Jacquemont S, Leehey MA, Hagerman RJ, Beckett LA, Hagerman PJ.

J Med Genet. 2006 Oct;43(10):804-9. Epub 2006 May 24.

14.

Brain structure in asymptomatic FMR1 premutation carriers at risk for fragile X-associated tremor/ataxia syndrome.

Battistella G, Niederhauser J, Fornari E, Hippolyte L, Gronchi Perrin A, Lesca G, Forzano F, Hagmann P, Vingerhoets FJ, Draganski B, Maeder P, Jacquemont S.

Neurobiol Aging. 2013 Jun;34(6):1700-7. doi: 10.1016/j.neurobiolaging.2012.12.001. Epub 2013 Jan 5.

PMID:
23298734
15.

Sleep apnea in fragile X premutation carriers with and without FXTAS.

Hamlin A, Liu Y, Nguyen DV, Tassone F, Zhang L, Hagerman RJ.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):923-8. doi: 10.1002/ajmg.b.31237. Epub 2011 Sep 19.

16.

High functioning male with fragile X syndrome and fragile X-associated tremor/ataxia syndrome.

Basuta K, Schneider A, Gane L, Polussa J, Woodruff B, Pretto D, Hagerman R, Tassone F.

Am J Med Genet A. 2015 Sep;167A(9):2154-61. doi: 10.1002/ajmg.a.37125. Epub 2015 Apr 29.

PMID:
25920745
17.

Expanded clinical phenotype of women with the FMR1 premutation.

Coffey SM, Cook K, Tartaglia N, Tassone F, Nguyen DV, Pan R, Bronsky HE, Yuhas J, Borodyanskaya M, Grigsby J, Doerflinger M, Hagerman PJ, Hagerman RJ.

Am J Med Genet A. 2008 Apr 15;146A(8):1009-16. doi: 10.1002/ajmg.a.32060.

18.

Fragile X premutation carriers: A systematic review of neuroimaging findings.

Brown SS, Stanfield AC.

J Neurol Sci. 2015 May 15;352(1-2):19-28. doi: 10.1016/j.jns.2015.03.031. Epub 2015 Mar 27. Review.

PMID:
25847019
19.

FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes.

Seixas AI, Vale J, Jorge P, Marques I, Santos R, Alonso I, Fortuna AM, Pinto-Basto J, Coutinho P, Margolis RL, Sequeiros J, Silveira I.

Behav Brain Funct. 2011 Jun 3;7:19. doi: 10.1186/1744-9081-7-19.

20.

Screening for the presence of FMR1 premutation alleles in women with parkinsonism.

Cilia R, Kraff J, Canesi M, Pezzoli G, Goldwurm S, Amiri K, Tang HT, Pan R, Hagerman PJ, Tassone F.

Arch Neurol. 2009 Feb;66(2):244-9. doi: 10.1001/archneurol.2008.548.

PMID:
19204162
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