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Items: 1 to 20 of 102

1.

Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation.

Kraan CM, Hocking DR, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Bradshaw JL, Cohen J, Cornish KM.

Neurobiol Aging. 2014 Sep;35(9):2179.e7-13. doi: 10.1016/j.neurobiolaging.2014.03.018. Epub 2014 Mar 20.

PMID:
24814676
2.

Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation.

Kraan CM, Hocking DR, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Bradshaw JL, Cohen J, Cornish KM.

Behav Brain Res. 2013 Sep 15;253:329-36. doi: 10.1016/j.bbr.2013.07.033. Epub 2013 Jul 27.

PMID:
23896050
3.

Delineation of the working memory profile in female FMR1 premutation carriers: the effect of cognitive load on ocular motor responses.

Shelton AL, Cornish KM, Godler DE, Clough M, Kraan C, Bui M, Fielding J.

Behav Brain Res. 2015 Apr 1;282:194-200. doi: 10.1016/j.bbr.2015.01.011. Epub 2015 Jan 13.

PMID:
25591477
4.

Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation.

Hocking DR, Kraan CM, Godler DE, Bui QM, Li X, Bradshaw JL, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Turbitt E, Fielding J, Trollor J, Cohen J, Cornish KM.

Neurobiol Aging. 2015 Mar;36(3):1400-8. doi: 10.1016/j.neurobiolaging.2014.11.012. Epub 2014 Nov 26.

PMID:
25541421
5.

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.

6.

Gait and Functional Mobility Deficits in Fragile X-Associated Tremor/Ataxia Syndrome.

O'Keefe JA, Robertson-Dick EE, Hall DA, Berry-Kravis E.

Cerebellum. 2016 Aug;15(4):475-82. doi: 10.1007/s12311-015-0714-4.

PMID:
26298472
7.

Selective executive markers of at-risk profiles associated with the fragile X premutation.

Cornish KM, Hocking DR, Moss SA, Kogan CS.

Neurology. 2011 Aug 16;77(7):618-22. doi: 10.1212/WNL.0b013e3182299e59. Epub 2011 Jul 20.

8.

Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS).

Van Dam D, Errijgers V, Kooy RF, Willemsen R, Mientjes E, Oostra BA, De Deyn PP.

Behav Brain Res. 2005 Jul 30;162(2):233-9.

PMID:
15876460
9.

Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers.

Kraan CM, Hocking DR, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Bradshaw JL, Cohen J, Cornish KM.

Am J Med Genet B Neuropsychiatr Genet. 2014 Jan;165B(1):41-51. doi: 10.1002/ajmg.b.32203. Epub 2013 Oct 26.

PMID:
24166828
10.

Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation.

Hocking DR, Kogan CS, Cornish KM.

Brain Cogn. 2012 Jun;79(1):39-44. doi: 10.1016/j.bandc.2012.02.005. Epub 2012 Mar 12.

PMID:
22417865
11.

Risk of cognitive impairment in female premutation carriers of fragile X premutation: analysis by means of robust segmented linear regression models.

Mínguez M, Ibáñez B, Ribate MP, Ramos F, García-Alegría E, Fernández-Rivas A, Ruiz-Parra E, Poch M, Alonso A, Martinez-Bouzas C, Beristain E, Tejada MI.

Am J Med Genet B Neuropsychiatr Genet. 2009 Mar 5;150B(2):262-70. doi: 10.1002/ajmg.b.30803.

PMID:
18563710
12.

Symbolic sequence learning is associated with cognitive-affective profiles in female FMR1 premutation carriers.

Kraan CM, Hocking DR, Bradshaw JL, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Cohen J, Cornish KM.

Genes Brain Behav. 2014 Apr;13(4):385-93. doi: 10.1111/gbb.12122. Epub 2014 Mar 11.

13.

Exploring inhibitory deficits in female premutation carriers of fragile X syndrome: through eye movements.

Shelton AL, Cornish K, Kraan C, Georgiou-Karistianis N, Metcalfe SA, Bradshaw JL, Hocking DR, Archibald AD, Cohen J, Trollor JN, Fielding J.

Brain Cogn. 2014 Mar;85:201-8. doi: 10.1016/j.bandc.2013.12.006. Epub 2014 Jan 11.

PMID:
24424424
14.

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.

15.

Mapping self-reports of working memory deficits to executive dysfunction in Fragile X Mental Retardation 1 (FMR1) gene premutation carriers asymptomatic for FXTAS.

Kogan CS, Cornish KM.

Brain Cogn. 2010 Aug;73(3):236-43. doi: 10.1016/j.bandc.2010.05.008. Epub 2010 Jun 22.

PMID:
20573435
16.

Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene.

Loesch DZ, Sherwell S, Kinsella G, Tassone F, Taylor A, Amor D, Sung S, Evans A.

Clin Genet. 2012 Jul;82(1):88-92. doi: 10.1111/j.1399-0004.2011.01675.x. Epub 2011 Apr 28.

PMID:
21476992
17.

Fragile X-associated tremor ataxia syndrome in FMR1 gray zone allele carriers.

Hall D, Tassone F, Klepitskaya O, Leehey M.

Mov Disord. 2012 Feb;27(2):296-300. doi: 10.1002/mds.24021. Epub 2011 Dec 11.

18.

Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.

Allen EG, Hunter JE, Rusin M, Juncos J, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SL.

Neuropsychology. 2011 May;25(3):404-11. doi: 10.1037/a0021879.

19.

The role of AGG interruptions in the transcription of FMR1 premutation alleles.

Yrigollen CM, Tassone F, Durbin-Johnson B, Tassone F.

PLoS One. 2011;6(7):e21728. doi: 10.1371/journal.pone.0021728. Epub 2011 Jul 19.

20.

Prevalence and predictors of subjective memory complaints in adult male carriers of the FMR1 premutation.

Birch RC, Hocking DR, Trollor JN.

Clin Neuropsychol. 2016 Aug;30(6):834-48. doi: 10.1080/13854046.2016.1145905. Epub 2016 Jun 29.

PMID:
27355815

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