Maglione V - Search Results

1

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: maglione v. 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

2

Cavernous angiomas of the nervous system in Italy: clinical and genetic study.

Squitieri F, Maglione V, Buzzi MG, Nargi E, Novelletto A, Cannella M, Simonelli M, Colonnese C, Simonelli P, Innocenzi G, Gagliardi FM, Caruso R, Ragona G, Cantore GP. Squitieri F, et al. Among authors: maglione v. Neurol Sci. 2000 Jun;21(3):129-34. doi: 10.1007/s100720070087. Neurol Sci. 2000. PMID: 11076000

3

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. Among authors: maglione v. 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.

4

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. Among authors: maglione v. Brain. 2003 Apr;126(Pt 4):946-55. doi: 10.1093/brain/awg077. Brain. 2003. PMID: 12615650

5

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. Among authors: maglione v. 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.

6

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. Among authors: maglione v. Neurol Sci. 2003 Oct;24(3):215-6. doi: 10.1007/s10072-003-0137-8. Neurol Sci. 2003. PMID: 14598094

7

Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations.

Liquori CL, Berg MJ, Siegel AM, Huang E, Zawistowski JS, Stoffer T, Verlaan D, Balogun F, Hughes L, Leedom TP, Plummer NW, Cannella M, Maglione V, Squitieri F, Johnson EW, Rouleau GA, Ptacek L, Marchuk DA. Liquori CL, et al. Among authors: maglione v. Am J Hum Genet. 2003 Dec;73(6):1459-64. doi: 10.1086/380314. Epub 2003 Nov 17. Am J Hum Genet. 2003. PMID: 14624391 Free PMC article.

8

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: maglione v. 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

9

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. 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

10

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. 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

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