Tassone F - Search Results

1

'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers.

Loesch DZ, Duffy DL, Martin NG, Tassone F, Atkinson A, Storey E. Loesch DZ, et al. Among authors: tassone f. Twin Res Hum Genet. 2021 Apr;24(2):95-102. doi: 10.1017/thg.2021.10. Epub 2021 Mar 24. Twin Res Hum Genet. 2021. PMID: 33757613

2

Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction.

Brunberg JA, Jacquemont S, Hagerman RJ, Berry-Kravis EM, Grigsby J, Leehey MA, Tassone F, Brown WT, Greco CM, Hagerman PJ. Brunberg JA, et al. Among authors: tassone f. AJNR Am J Neuroradiol. 2002 Nov-Dec;23(10):1757-66. AJNR Am J Neuroradiol. 2002. PMID: 12427636 Free PMC article.

3

Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates.

Jacquemont S, Hagerman RJ, Leehey M, Grigsby J, Zhang L, Brunberg JA, Greco C, Des Portes V, Jardini T, Levine R, Berry-Kravis E, Brown WT, Schaeffer S, Kissel J, Tassone F, Hagerman PJ. Jacquemont S, et al. Among authors: tassone f. Am J Hum Genet. 2003 Apr;72(4):869-78. doi: 10.1086/374321. Epub 2003 Mar 12. Am J Hum Genet. 2003. PMID: 12638084 Free PMC article.

4

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome.

Willemsen R, Hoogeveen-Westerveld M, Reis S, Holstege J, Severijnen LA, Nieuwenhuizen IM, Schrier M, van Unen L, Tassone F, Hoogeveen AT, Hagerman PJ, Mientjes EJ, Oostra BA. Willemsen R, et al. Among authors: tassone f. Hum Mol Genet. 2003 May 1;12(9):949-59. doi: 10.1093/hmg/ddg114. Hum Mol Genet. 2003. PMID: 12700164 Free article.

5

The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter.

Chen LS, Tassone F, Sahota P, Hagerman PJ. Chen LS, et al. Among authors: tassone f. Hum Mol Genet. 2003 Dec 1;12(23):3067-74. doi: 10.1093/hmg/ddg331. Epub 2003 Sep 30. Hum Mol Genet. 2003. PMID: 14519687

6

Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element.

Beilina A, Tassone F, Schwartz PH, Sahota P, Hagerman PJ. Beilina A, et al. Among authors: tassone f. Hum Mol Genet. 2004 Mar 1;13(5):543-9. doi: 10.1093/hmg/ddh053. Epub 2004 Jan 13. Hum Mol Genet. 2004. PMID: 14722156

7

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. Jacquemont S, et al. Among authors: tassone f. JAMA. 2004 Jan 28;291(4):460-9. doi: 10.1001/jama.291.4.460. JAMA. 2004. PMID: 14747503

8

Screen for expanded FMR1 alleles in patients with essential tremor.

Garcia Arocena D, Louis ED, Tassone F, Gilliam TC, Ottman R, Jacquemont S, Hagerman PJ. Garcia Arocena D, et al. Among authors: tassone f. Mov Disord. 2004 Aug;19(8):930-3. doi: 10.1002/mds.20043. Mov Disord. 2004. PMID: 15300658

9

Magnetic resonance imaging study in older fragile X premutation male carriers.

Loesch DZ, Litewka L, Brotchie P, Huggins RM, Tassone F, Cook M. Loesch DZ, et al. Among authors: tassone f. Ann Neurol. 2005 Aug;58(2):326-30. doi: 10.1002/ana.20542. Ann Neurol. 2005. PMID: 16049924

10

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.

Hessl D, Tassone F, Loesch DZ, Berry-Kravis E, Leehey MA, Gane LW, Barbato I, Rice C, Gould E, Hall DA, Grigsby J, Wegelin JA, Harris S, Lewin F, Weinberg D, Hagerman PJ, Hagerman RJ. Hessl D, et al. Among authors: tassone f. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):115-21. doi: 10.1002/ajmg.b.30241. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16184602

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