Squitieri F - Search Results

1

Huntingtin Haplotypes Provide Prioritized Target Panels for Allele-specific Silencing in Huntington Disease Patients of European Ancestry.

Kay C, Collins JA, Skotte NH, Southwell AL, Warby SC, Caron NS, Doty CN, Nguyen B, Griguoli A, Ross CJ, Squitieri F, Hayden MR. Kay C, et al. Among authors: squitieri f. Mol Ther. 2015 Nov;23(11):1759-1771. doi: 10.1038/mt.2015.128. Epub 2015 Jul 23. Mol Ther. 2015. PMID: 26201449 Free PMC article.

2

Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases.

Goldberg YP, Andrew SE, Theilmann J, Kremer B, Squitieri F, Telenius H, Brown JD, Hayden MR. Goldberg YP, et al. Among authors: squitieri f. J Med Genet. 1993 Dec;30(12):987-90. doi: 10.1136/jmg.30.12.987. J Med Genet. 1993. PMID: 8133509 Free PMC article.

3

Molecular analysis of late onset Huntington's disease.

Kremer B, Squitieri F, Telenius H, Andrew SE, Theilmann J, Spence N, Goldberg YP, Hayden MR. Kremer B, et al. Among authors: squitieri f. J Med Genet. 1993 Dec;30(12):991-5. doi: 10.1136/jmg.30.12.991. J Med Genet. 1993. PMID: 8133510 Free PMC article.

4

Update on genetics of Huntington's disease: availability of direct and accurate predictive test.

Squitieri F, Campanella G, Hayden MR. Squitieri F, et al. Ital J Neurol Sci. 1996 Jun;17(3):185-7. doi: 10.1007/BF01995681. Ital J Neurol Sci. 1996. PMID: 8856407 No abstract available.

5

Presymptomatic tests in Huntington's disease and dominant ataxias.

Cannella M, Simonelli M, D'Alessio C, Pierelli F, Ruggieri S, Squitieri F. Cannella M, et al. Among authors: squitieri f. Neurol Sci. 2001 Feb;22(1):55-6. doi: 10.1007/s100720170044. Neurol Sci. 2001. PMID: 11487199

6

Onset and pre-onset studies to define the Huntington's disease natural history.

Squitieri F, Cannella M, Giallonardo P, Maglione V, Mariotti C, Hayden MR. Squitieri F, et al. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):233-8. doi: 10.1016/s0361-9230(01)00648-7. Brain Res Bull. 2001. PMID: 11719256 Review.

7

CAG mutation effect on rate of progression in Huntington's disease.

Squitieri F, Cannella M, Simonelli M. Squitieri F, et al. Neurol Sci. 2002 Sep;23 Suppl 2:S107-8. doi: 10.1007/s100720200092. Neurol Sci. 2002. PMID: 12548366

8

Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course.

Squitieri F, Gellera C, Cannella M, Mariotti C, Cislaghi G, Rubinsztein DC, Almqvist EW, Turner D, Bachoud-Lévi AC, Simpson SA, Delatycki M, Maglione V, Hayden MR, Donato SD. Squitieri F, et al. Brain. 2003 Apr;126(Pt 4):946-55. doi: 10.1093/brain/awg077. Brain. 2003. PMID: 12615650

9

Italian Huntington disease patients--data and tissue bank.

Squitieri F, Cannella M, Gaudio L, Martino T, Maglione V, Giallonardo P, Simonelli M, Simonelli G, Mangeruga D, Ciarmiello A, Pierelli F. Squitieri F, et al. Neurol Sci. 2003 Oct;24(3):215-6. doi: 10.1007/s10072-003-0137-8. Neurol Sci. 2003. PMID: 14598094

10

The gender effect in juvenile Huntington disease patients of Italian origin.

Cannella M, Gellera C, Maglione V, Giallonardo P, Cislaghi G, Muglia M, Quattrone A, Pierelli F, Di Donato S, Squitieri F. Cannella M, et al. Among authors: squitieri f. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):92-8. doi: 10.1002/ajmg.b.20110. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755452

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