Cislaghi G - Search Results

1

Huntington's disease: the current state of research with peripheral tissues.

Sassone J, Colciago C, Cislaghi G, Silani V, Ciammola A. Sassone J, et al. Among authors: cislaghi g. Exp Neurol. 2009 Oct;219(2):385-97. doi: 10.1016/j.expneurol.2009.05.012. Epub 2009 May 19. Exp Neurol. 2009. PMID: 19460373 Review.

2

Aberrant A2A receptor function in peripheral blood cells in Huntington's disease.

Varani K, Abbracchio MP, Cannella M, Cislaghi G, Giallonardo P, Mariotti C, Cattabriga E, Cattabeni F, Borea PA, Squitieri F, Cattaneo E. Varani K, et al. Among authors: cislaghi g. FASEB J. 2003 Nov;17(14):2148-50. doi: 10.1096/fj.03-0079fje. Epub 2003 Sep 4. FASEB J. 2003. PMID: 12958155

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

4

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: cislaghi g. 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

5

Huntingtin fragmentation and increased caspase 3, 8 and 9 activities in lymphoblasts with heterozygous and homozygous Huntington's disease mutation.

Maglione V, Cannella M, Gradini R, Cislaghi G, Squitieri F. Maglione V, et al. Among authors: cislaghi g. Mech Ageing Dev. 2006 Feb;127(2):213-6. doi: 10.1016/j.mad.2005.09.011. Epub 2005 Nov 10. Mech Ageing Dev. 2006. PMID: 16289252

6

Cause and course in a series of patients with sporadic chorea.

Piccolo I, Defanti CA, Soliveri P, Volontè MA, Cislaghi G, Girotti F. Piccolo I, et al. Among authors: cislaghi g. J Neurol. 2003 Apr;250(4):429-35. doi: 10.1007/s00415-003-1010-7. J Neurol. 2003. PMID: 12700907

7

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. Among authors: cislaghi g. 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

8

Neuroanatomical, Clinical and Cognitive Correlates of Post-Stroke Dysphagia.

Toscano M, Cecconi E, Capiluppi E, Viganò A, Bertora P, Campiglio L, Mariani C, Petolicchio B, Sasso D'Elia T, Verzina A, Vicenzini E, Fiorelli M, Cislaghi G, Di Piero V. Toscano M, et al. Among authors: cislaghi g. Eur Neurol. 2015;74(3-4):171-7. doi: 10.1159/000441056. Epub 2015 Oct 23. Eur Neurol. 2015. PMID: 26492033

9

Predictive testing for persons at risk for homozygosity for CAG expansion in the Huntington disease gene.

Squitieri F, Almqvist EW, Cannella M, Cislaghi G, Hayden MR. Squitieri F, et al. Among authors: cislaghi g. Clin Genet. 2003 Dec;64(6):524-5. doi: 10.1046/j.1399-0004.2003.00155.x. Clin Genet. 2003. PMID: 14986835 No abstract available.

10

An unusual case of PML in HIV patient presenting with diplopia.

Romano L, Capiluppi E, Macerollo A, Cislaghi G. Romano L, et al. Among authors: cislaghi g. Neurol Sci. 2019 May;40(5):1081-1082. doi: 10.1007/s10072-018-3665-y. Epub 2018 Dec 5. Neurol Sci. 2019. PMID: 30515605 No abstract available.

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