Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 81

1.

White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism.

Loesch DZ, Kotschet K, Trost N, Greco CM, Kinsella G, Slater HR, Venn A, Horne M.

Am J Med Genet B Neuropsychiatr Genet. 2011 Jun;156B(4):502-6. doi: 10.1002/ajmg.b.31189. Epub 2011 Mar 28.

2.

White matter changes in patients with Parkinson's disease carrying small CGG expansion FMR1 alleles: a pilot study.

Trost N, Cook M, Hammersley E, Bui MQ, Brotchie P, Burgess T, Slater H, Storey E, Loesch DZ.

Neurodegener Dis. 2014;14(2):67-76. doi: 10.1159/000356190. Epub 2013 Dec 24.

PMID:
24401315
3.

Clinical Phenotype of Adult Fragile X Gray Zone Allele Carriers: a Case Series.

Debrey SM, Leehey MA, Klepitskaya O, Filley CM, Shah RC, Kluger B, Berry-Kravis E, Spector E, Tassone F, Hall DA.

Cerebellum. 2016 Oct;15(5):623-31. doi: 10.1007/s12311-016-0809-6.

PMID:
27372099
4.

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
5.

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.

6.

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.

7.

Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism.

Entezari A, Khaniani MS, Bahrami T, Derakhshan SM, Darvish H.

Neurol Sci. 2017 Jan;38(1):123-128. doi: 10.1007/s10072-016-2723-6. Epub 2016 Oct 1.

PMID:
27696273
8.

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism.

Loesch DZ, Khaniani MS, Slater HR, Rubio JP, Bui QM, Kotschet K, D'Souza W, Venn A, Kalitsis P, Choo AK, Burgess T, Johnson L, Evans A, Horne M.

Clin Genet. 2009 Nov;76(5):471-6. doi: 10.1111/j.1399-0004.2009.01275.x. Epub 2009 Sep 30.

9.

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.

10.

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.

11.

Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism.

Loesch DZ, Godler DE, Evans A, Bui QM, Gehling F, Kotschet KE, Trost N, Storey E, Stimpson P, Kinsella G, Francis D, Thorburn DR, Venn A, Slater HR, Horne M.

Genet Med. 2011 May;13(5):392-9. doi: 10.1097/GIM.0b013e3182064362.

12.

FMR1 gray-zone alleles: association with Parkinson's disease in women?

Hall DA, Berry-Kravis E, Zhang W, Tassone F, Spector E, Zerbe G, Hagerman PJ, Ouyang B, Leehey MA.

Mov Disord. 2011 Aug 15;26(10):1900-6. doi: 10.1002/mds.23755. Epub 2011 May 12.

13.

Genetic analysis of FMR1 repeat expansion in essential tremor.

Clark LN, Ye X, Liu X, Louis ED.

Neurosci Lett. 2015 Apr 23;593:114-7. doi: 10.1016/j.neulet.2015.03.027. Epub 2015 Mar 18.

14.

Expansion of an FMR1 grey-zone allele to a full mutation in two generations.

Fernandez-Carvajal I, Lopez Posadas B, Pan R, Raske C, Hagerman PJ, Tassone F.

J Mol Diagn. 2009 Jul;11(4):306-10. doi: 10.2353/jmoldx.2009.080174. Epub 2009 Jun 12.

15.

Parkinsonism, FXTAS, and FMR1 premutations.

Toft M, Aasly J, Bisceglio G, Adler CH, Uitti RJ, Krygowska-Wajs A, Lynch T, Wszolek ZK, Farrer MJ.

Mov Disord. 2005 Feb;20(2):230-3.

PMID:
15390127
16.

Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China.

Zhang X, Zhuang X, Gan S, Wu Z, Chen W, Hu Y, Wang N.

Neurosci Lett. 2012 Apr 11;514(1):16-21. doi: 10.1016/j.neulet.2012.02.036. Epub 2012 Feb 22.

PMID:
22387066
17.

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.

PMID:
16332642
18.

Immune dysregulation as a cause of autoinflammation in fragile X premutation carriers: link between FMRI CGG repeat number and decreased cytokine responses.

Careaga M, Rose D, Tassone F, Berman RF, Hagerman R, Ashwood P.

PLoS One. 2014 Apr 9;9(4):e94475. doi: 10.1371/journal.pone.0094475. eCollection 2014.

19.

The significance of fragile X mental retardation gene 1 CGG repeat sizes in the normal and intermediate range in women with primary ovarian insufficiency.

Voorhuis M, Onland-Moret NC, Janse F, Ploos van Amstel HK, Goverde AJ, Lambalk CB, Laven JS, van der Schouw YT, Broekmans FJ, Fauser BC; Dutch Primary Ovarian Insufficiency Consortium.

Hum Reprod. 2014 Jul;29(7):1585-93. doi: 10.1093/humrep/deu095. Epub 2014 May 7.

PMID:
24812319
20.

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 16;271(7):507-14.

PMID:
8301764

Supplemental Content

Support Center