Tassone F - Search Results

1

Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond.

Loesch DZ, Churchyard A, Brotchie P, Marot M, Tassone F. Loesch DZ, et al. Among authors: tassone f. Clin Genet. 2005 May;67(5):412-7. doi: 10.1111/j.1399-0004.2005.00425.x. Clin Genet. 2005. PMID: 15811008

2

Tremor/ataxia syndrome and fragile X premutation: diagnostic caveats.

Loesch DZ, Litewka L, Churchyard A, Gould E, Tassone F, Cook M. Loesch DZ, et al. Among authors: tassone f. J Clin Neurosci. 2007 Mar;14(3):245-8. doi: 10.1016/j.jocn.2006.01.015. Epub 2006 Dec 27. J Clin Neurosci. 2007. PMID: 17194594

3

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. Loesch DZ, et al. Among authors: tassone f. Clin Genet. 2012 Jul;82(1):88-92. doi: 10.1111/j.1399-0004.2011.01675.x. Epub 2011 Apr 28. Clin Genet. 2012. PMID: 21476992

4

New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease.

Loesch DZ, Tassone F, Lo J, Slater HR, Hills LV, Bui MQ, Silburn PA, Mellick GD. Loesch DZ, et al. Among authors: tassone f. Clin Genet. 2013 Oct;84(4):382-5. doi: 10.1111/cge.12070. Epub 2012 Dec 25. Clin Genet. 2013. PMID: 23198693

5

Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion.

Loesch DZ, Bui MQ, Hammersley E, Schneider A, Storey E, Stimpson P, Burgess T, Francis D, Slater H, Tassone F, Hagerman RJ, Hessl D. Loesch DZ, et al. Among authors: tassone f. Clin Genet. 2015 Feb;87(2):173-8. doi: 10.1111/cge.12347. Epub 2014 Feb 17. Clin Genet. 2015. PMID: 24428240 Free PMC article.

6

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Tassone F, et al. Am J Med Genet. 2000 Sep 18;94(3):232-6. doi: 10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10995510

7

A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes.

Loesch DZ, Cook M, Litewka L, Gould E, Churchyard A, Tassone F, Slater HR, Storey E. Loesch DZ, et al. Among authors: tassone f. J Med Genet. 2008 Mar;45(3):179-81. doi: 10.1136/jmg.2007.054171. Epub 2007 Dec 5. J Med Genet. 2008. PMID: 18057083

8

Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome.

Cohen S, Masyn K, Adams J, Hessl D, Rivera S, Tassone F, Brunberg J, DeCarli C, Zhang L, Cogswell J, Loesch D, Leehey M, Grigsby J, Hagerman PJ, Hagerman R. Cohen S, et al. Among authors: tassone f. Neurology. 2006 Oct 24;67(8):1426-31. doi: 10.1212/01.wnl.0000239837.57475.3a. Neurology. 2006. PMID: 17060569

9

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

Liu Y, Winarni TI, Zhang L, Tassone F, Hagerman RJ. Liu Y, et al. Among authors: tassone f. Clin Genet. 2013 Jul;84(1):74-7. doi: 10.1111/cge.12026. Epub 2012 Oct 17. Clin Genet. 2013. PMID: 23009394 Free PMC article.

10

FXTAS in an unmethylated mosaic male with fragile X syndrome from Chile.

Santa María L, Pugin A, Alliende MA, Aliaga S, Curotto B, Aravena T, Tang HT, Mendoza-Morales G, Hagerman R, Tassone F. Santa María L, et al. Among authors: tassone f. Clin Genet. 2014 Oct;86(4):378-82. doi: 10.1111/cge.12278. Epub 2013 Oct 13. Clin Genet. 2014. PMID: 24028275 Free PMC article.

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