Similar articles for PMID: 27696273

Year	Number of Results
2003	1
2004	2
2005	6
2006	7
2007	7
2008	6
2009	4
2010	1
2011	5
2012	7
2013	4
2014	7
2015	6
2016	4
2017	6
2018	5
2019	1
2020	3
2021	2
2022	1
2024	0

1

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

Entezari A, Khaniani MS, Bahrami T, Derakhshan SM, Darvish H. Entezari A, et al. Neurol Sci. 2017 Jan;38(1):123-128. doi: 10.1007/s10072-016-2723-6. Epub 2016 Oct 1. Neurol Sci. 2017. PMID: 27696273

2

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

Jacquemont S, Leehey MA, Hagerman RJ, Beckett LA, Hagerman PJ. Jacquemont S, et al. J Med Genet. 2006 Oct;43(10):804-9. doi: 10.1136/jmg.2006.042374. Epub 2006 May 24. J Med Genet. 2006. PMID: 16723388 Free PMC article.

3

Parkinsonism, FXTAS, and FMR1 premutations.

Toft M, Aasly J, Bisceglio G, Adler CH, Uitti RJ, Krygowska-Wajs A, Lynch T, Wszolek ZK, Farrer MJ. Toft M, et al. Mov Disord. 2005 Feb;20(2):230-3. doi: 10.1002/mds.20297. Mov Disord. 2005. PMID: 15390127

4

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. Debrey SM, et al. Cerebellum. 2016 Oct;15(5):623-31. doi: 10.1007/s12311-016-0809-6. Cerebellum. 2016. PMID: 27372099

5

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. Loesch DZ, et al. Clin Genet. 2009 Nov;76(5):471-6. doi: 10.1111/j.1399-0004.2009.01275.x. Epub 2009 Sep 30. Clin Genet. 2009. PMID: 19796183 Free PMC article.

6

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. Cilia R, et al. Arch Neurol. 2009 Feb;66(2):244-9. doi: 10.1001/archneurol.2008.548. Arch Neurol. 2009. PMID: 19204162

7

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. Zhang X, et al. Neurosci Lett. 2012 Apr 11;514(1):16-21. doi: 10.1016/j.neulet.2012.02.036. Epub 2012 Feb 22. Neurosci Lett. 2012. PMID: 22387066

8

Evidence for the role of FMR1 gray zone alleles as a risk factor for parkinsonism in females.

Loesch DZ, Tassone F, Mellick GD, Horne M, Rubio JP, Bui MQ, Francis D, Storey E. Loesch DZ, et al. Mov Disord. 2018 Jul;33(7):1178-1181. doi: 10.1002/mds.27420. Mov Disord. 2018. PMID: 30153395 Free PMC article.

9

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. Hall DA, et al. Mov Disord. 2011 Aug 15;26(10):1900-6. doi: 10.1002/mds.23755. Epub 2011 May 12. Mov Disord. 2011. PMID: 21567456 Free PMC article.

10

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. Loesch DZ, et al. Genet Med. 2011 May;13(5):392-9. doi: 10.1097/GIM.0b013e3182064362. Genet Med. 2011. PMID: 21270637 Free PMC article.

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