Mariani C - Search Results

1

Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's disease.

Galimberti D, Venturelli E, Gatti A, Lovati C, Fenoglio C, Mariani C, Forloni G, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: mariani c. J Neurol. 2005 Aug;252(8):985-6. doi: 10.1007/s00415-005-0783-2. Epub 2005 Mar 17. J Neurol. 2005. PMID: 15765269 No abstract available.

2

CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration.

Villa C, Venturelli E, Fenoglio C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Cortini F, Scalabrini D, Serpente M, Binetti G, Cappa S, Mariani C, Rainero I, Bresolin N, Scarpini E, Galimberti D. Villa C, et al. Among authors: mariani c. J Neurol. 2009 Aug;256(8):1379-81. doi: 10.1007/s00415-009-5138-y. Epub 2009 May 5. J Neurol. 2009. PMID: 19415413

3

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.

Venturelli E, Villa C, Scarpini E, Fenoglio C, Guidi I, Lovati C, Marcone A, Cortini F, Scalabrini D, Clerici F, Bresolin N, Mariani C, Cappa S, Galimberti D. Venturelli E, et al. Among authors: mariani c. Eur J Neurol. 2008 Jan;15(1):77-81. doi: 10.1111/j.1468-1331.2007.02007.x. Epub 2007 Nov 27. Eur J Neurol. 2008. PMID: 18042235

4

The T-786C NOS3 polymorphism in Alzheimer's disease: association and influence on gene expression.

Venturelli E, Galimberti D, Lovati C, Fenoglio C, Scalabrini D, Mariani C, Forloni G, Bresolin N, Scarpini E. Venturelli E, et al. Among authors: mariani c. Neurosci Lett. 2005 Jul 15;382(3):300-3. doi: 10.1016/j.neulet.2005.03.032. Epub 2005 Apr 7. Neurosci Lett. 2005. PMID: 15925107

5

Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's disease in Italy.

Albani D, Vittori A, Batelli S, Polito L, De Mauro S, Galimberti D, Scarpini E, Lovati C, Mariani C, Forloni G. Albani D, et al. Among authors: mariani c. Eur Neurol. 2009;62(2):120-3. doi: 10.1159/000222784. Epub 2009 Jun 12. Eur Neurol. 2009. PMID: 19521089

6

Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease.

Cortini F, Fenoglio C, Venturelli E, Villa C, Clerici F, Serpente M, Cantoni C, Fumagalli G, Mariani C, Bresolin N, Scarpini E, Galimberti D. Cortini F, et al. Among authors: mariani c. J Neurol. 2011 Apr;258(4):704-5. doi: 10.1007/s00415-010-5816-9. Epub 2010 Nov 11. J Neurol. 2011. PMID: 21069533 No abstract available.

7

MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levels.

Fenoglio C, Galimberti D, Lovati C, Guidi I, Gatti A, Fogliarino S, Tiriticco M, Mariani C, Forloni G, Pettenati C, Baron P, Conti G, Bresolin N, Scarpini E. Fenoglio C, et al. Among authors: mariani c. Neurobiol Aging. 2004 Oct;25(9):1169-73. doi: 10.1016/j.neurobiolaging.2003.11.008. Neurobiol Aging. 2004. PMID: 15312962

8

CCR2-64I polymorphism and CCR5Delta32 deletion in patients with Alzheimer's disease.

Galimberti D, Fenoglio C, Lovati C, Gatti A, Guidi I, Venturelli E, Cutter GR, Mariani C, Forloni G, Pettenati C, Baron P, Conti G, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: mariani c. J Neurol Sci. 2004 Oct 15;225(1-2):79-83. doi: 10.1016/j.jns.2004.07.005. J Neurol Sci. 2004. PMID: 15465089

9

CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical course.

Galimberti D, Scalabrini D, Fenoglio C, Comi C, De Riz M, Venturelli E, Lovati C, Mariani C, Monaco F, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: mariani c. Eur J Neurol. 2007 Feb;14(2):162-7. doi: 10.1111/j.1468-1331.2006.01629.x. Eur J Neurol. 2007. PMID: 17250724

10

IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease.

Galimberti D, Venturelli E, Fenoglio C, Lovati C, Guidi I, Scalabrini D, Mariani C, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: mariani c. Eur J Neurol. 2007 Apr;14(4):e3-4. doi: 10.1111/j.1468-1331.2006.01637.x. Eur J Neurol. 2007. PMID: 17388976 No abstract available.

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