Squitieri F - Search Results

1

Tractography of the corpus callosum in Huntington's disease.

Phillips O, Sanchez-Castaneda C, Elifani F, Maglione V, Di Pardo A, Caltagirone C, Squitieri F, Sabatini U, Di Paola M. Phillips O, et al. Among authors: squitieri f. PLoS One. 2013 Sep 3;8(9):e73280. doi: 10.1371/journal.pone.0073280. eCollection 2013. PLoS One. 2013. PMID: 24019913 Free PMC article.

2

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.

3

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

4

Highly disabling cerebellar presentation in Huntington disease.

Squitieri F, Pustorino G, Cannella M, Toscano A, Maglione V, Morgante L, Tortorella G. Squitieri F, et al. Eur J Neurol. 2003 Jul;10(4):443-4. doi: 10.1046/j.1468-1331.2003.00601.x. Eur J Neurol. 2003. PMID: 12823498 No abstract available.

5

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

6

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

7

New Huntington disease mutation arising from a paternal CAG34 allele showing somatic length variation in serially passaged lymphoblasts.

Cannella M, Maglione V, Martino T, Simonelli M, Ragona G, Squitieri F. Cannella M, et al. Among authors: squitieri f. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):127-30. doi: 10.1002/ajmg.b.30125. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15546151

8

Adenosine A2A receptor dysfunction correlates with age at onset anticipation in blood platelets of subjects with Huntington's disease.

Maglione V, Giallonardo P, Cannella M, Martino T, Frati L, Squitieri F. Maglione V, et al. Among authors: squitieri f. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):101-5. doi: 10.1002/ajmg.b.30223. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16184606

9

The platelet maximum number of A2A-receptor binding sites (Bmax) linearly correlates with age at onset and CAG repeat expansion in Huntington's disease patients with predominant chorea.

Maglione V, Cannella M, Martino T, De Blasi A, Frati L, Squitieri F. Maglione V, et al. Among authors: squitieri f. Neurosci Lett. 2006 Jan 23;393(1):27-30. doi: 10.1016/j.neulet.2005.09.037. Epub 2005 Oct 10. Neurosci Lett. 2006. PMID: 16221531

10

Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for Huntington disease mutation.

Squitieri F, Cannella M, Sgarbi G, Maglione V, Falleni A, Lenzi P, Baracca A, Cislaghi G, Saft C, Ragona G, Russo MA, Thompson LM, Solaini G, Fornai F. Squitieri F, et al. Mech Ageing Dev. 2006 Feb;127(2):217-20. doi: 10.1016/j.mad.2005.09.010. Epub 2005 Nov 9. Mech Ageing Dev. 2006. PMID: 16289240

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