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Items: 32

1.

GSK3β genetic variability in patients with Multiple Sclerosis.

Galimberti D, Macmurray J, Scalabrini D, Fenoglio C, De Riz M, Comi C, Comings D, Cortini F, Villa C, Serpente M, Cantoni C, Ridolfi E, Fardipoor MH, Leone M, Monaco F, Bresolin N, Scarpini E.

Neurosci Lett. 2011 Jun 15;497(1):46-8. doi: 10.1016/j.neulet.2011.04.024. Epub 2011 Apr 17.

PMID:
21527318
2.

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Scalabrini D, Cortini F, Fumagalli G, Cappa S, Binetti G, Franceschi M, Rainero I, Giordana MT, Mariani C, Bresolin N, Scarpini E, Galimberti D.

Neurosci Lett. 2010 Oct 4;482(3):240-4. doi: 10.1016/j.neulet.2010.07.047. Epub 2010 Jul 27.

PMID:
20670673
3.

Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males.

Fenoglio C, Scalabrini D, Esposito F, Comi C, Cavalla P, De Riz M, Martinelli V, Piccio LM, Venturelli E, Fumagalli G, Capra R, Collimedaglia L, Ghezzi A, Rodegher ME, Vercellino M, Leone M, Giordana MT, Bresolin N, Monaco F, Comi G, Scarpini E, Martinelli-Boneschi F, Galimberti D.

Genes Immun. 2010 Sep;11(6):497-503. doi: 10.1038/gene.2010.18. Epub 2010 May 13.

PMID:
20463744
4.

Loss of epidermal growth factor regulation by cobalamin in multiple sclerosis.

Scalabrino G, Galimberti D, Mutti E, Scalabrini D, Veber D, De Riz M, Bamonti F, Capello E, Mancardi GL, Scarpini E.

Brain Res. 2010 May 28;1333:64-71. doi: 10.1016/j.brainres.2010.03.073. Epub 2010 Mar 27.

PMID:
20347721
5.

Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort.

Martinelli-Boneschi F, Esposito F, Scalabrini D, Fenoglio C, Rodegher ME, Brambilla P, Colombo B, Ghezzi A, Capra R, Collimedaglia L, Coniglio G, De Riz M, Serpente M, Cantoni C, Scarpini E, Martinelli V, Galimberti D, Comi G.

Eur J Neurol. 2010 May;17(5):740-5. doi: 10.1111/j.1468-1331.2009.02925.x. Epub 2010 Jan 7.

PMID:
20067515
6.

GRN variability contributes to sporadic frontotemporal lobar degeneration.

Galimberti D, Fenoglio C, Cortini F, Serpente M, Venturelli E, Villa C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Scalabrini D, Restelli I, Martinelli Boneschi F, Cappa S, Binetti G, Mariani C, Rainero I, Giordana MT, Bresolin N, Scarpini E.

J Alzheimers Dis. 2010;19(1):171-7. doi: 10.3233/JAD-2010-1225.

PMID:
20061636
7.

FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration.

Cantoni C, Fenoglio C, Cortini F, Venturelli E, Villa C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Scalabrini D, Franceschi M, Cappa S, Binetti G, Mariani C, Rainero I, Giordana MT, Bresolin N, Scarpini E, Galimberti D.

J Alzheimers Dis. 2010;19(4):1317-22. doi: 10.3233/JAD-2010-1328.

PMID:
20061612
8.

Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypes.

De Riz M, Galimberti D, Fenoglio C, Piccio LM, Scalabrini D, Venturelli E, Pietroboni A, Piola M, Naismith RT, Parks BJ, Fumagalli G, Bresolin N, Cross AH, Scarpini E.

Neurosci Lett. 2010 Jan 22;469(2):234-6. doi: 10.1016/j.neulet.2009.12.002. Epub 2009 Dec 4.

9.

Candidate gene analysis of semaphorins in patients with Alzheimer's disease.

Villa C, Venturelli E, Fenoglio C, De Riz M, Scalabrini D, Cortini F, Serpente M, Cantoni C, Bresolin N, Scarpini E, Galimberti D.

Neurol Sci. 2010 Apr;31(2):169-73. doi: 10.1007/s10072-009-0200-1. Epub 2009 Dec 3.

PMID:
19957197
10.

Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.

Fenoglio C, Galimberti D, Cortini F, Kauwe JS, Cruchaga C, Venturelli E, Villa C, Serpente M, Scalabrini D, Mayo K, Piccio LM, Clerici F, Albani D, Mariani C, Forloni G, Bresolin N, Goate AM, Scarpini E.

J Alzheimers Dis. 2009;18(3):603-12. doi: 10.3233/JAD-2009-1170.

11.

MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels.

Galimberti D, Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Cortini F, Scalabrini D, Perini L, Restelli I, Binetti G, Cappa S, Mariani C, Bresolin N, Scarpini E.

J Alzheimers Dis. 2009;17(1):125-33. doi: 10.3233/JAD-2009-1019.

PMID:
19494437
12.

DCUN1D1 is a risk factor for frontotemporal lobar degeneration.

Villa C, Venturelli E, Fenoglio C, Clerici F, Marcone A, Benussi L, Gallone S, Scalabrini D, Cortini F, Serpente M, Martinelli Boneschi F, Cappa S, Binetti G, Mariani C, Rainero I, Giordana MT, Bresolin N, Scarpini E, Galimberti D.

Eur J Neurol. 2009 Jul;16(7):870-3. doi: 10.1111/j.1468-1331.2009.02611.x. Epub 2009 Mar 31.

PMID:
19473369
13.

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.

J Neurol. 2009 Aug;256(8):1379-81. doi: 10.1007/s00415-009-5138-y. Epub 2009 May 5.

PMID:
19415413
14.

Candidate gene analysis of selectin cluster in patients with multiple sclerosis.

Fenoglio C, Scalabrini D, Piccio L, De Riz M, Venturelli E, Cortini F, Villa C, Serpente M, Parks B, Rinker J, Cross AH, Bresolin N, Scarpini E, Galimberti D.

J Neurol. 2009 May;256(5):832-3. doi: 10.1007/s00415-009-5016-7. Epub 2009 Feb 25.

PMID:
19240957
15.

The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.

Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Ghidoni R, Cortini F, Scalabrini D, Gallone S, Rainero I, Mandelli A, Restelli I, Binetti G, Cappa S, Mariani C, Giordana MT, Bresolin N, Scarpini E, Galimberti D.

Eur J Neurol. 2009 Jan;16(1):37-42. doi: 10.1111/j.1468-1331.2008.02335.x.

PMID:
19087148
16.

Novel exon 1 progranulin gene variant in Alzheimer's disease.

Cortini F, Fenoglio C, Guidi I, Venturelli E, Pomati S, Marcone A, Scalabrini D, Villa C, Clerici F, Dalla Valle E, Mariani C, Cappa S, Bresolin N, Scarpini E, Galimberti D.

Eur J Neurol. 2008 Oct;15(10):1111-7. doi: 10.1111/j.1468-1331.2008.02266.x. Epub 2008 Aug 26.

PMID:
18752597
17.

MDC/CCL22 intrathecal levels in patients with multiple sclerosis.

Galimberti D, Fenoglio C, Comi C, Scalabrini D, De Riz M, Leone M, Venturelli E, Cortini F, Piola M, Monaco F, Bresolin N, Scarpini E.

Mult Scler. 2008 May;14(4):547-9. doi: 10.1177/1352458507084268. Epub 2008 Jan 21.

PMID:
18208895
18.

Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration.

Galimberti D, Venturelli E, Fenoglio C, Guidi I, Villa C, Bergamaschini L, Cortini F, Scalabrini D, Baron P, Vergani C, Bresolin N, Scarpini E.

J Neurol. 2008 Apr;255(4):539-44. doi: 10.1007/s00415-008-0737-6. Epub 2008 Jan 23.

PMID:
18204920
19.

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.

Eur J Neurol. 2008 Jan;15(1):77-81. Epub 2007 Nov 27.

PMID:
18042235
20.

Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis.

Galimberti D, Scalabrini D, Fenoglio C, De Riz M, Comi C, Venturelli E, Cortini F, Piola M, Leone M, Dianzani U, D'Alfonso S, Monaco F, Bresolin N, Scarpini E.

J Neurol Sci. 2008 Apr 15;267(1-2):86-90. Epub 2007 Oct 29.

PMID:
17967467
21.

Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis.

Scalabrini D, Fenoglio C, Scarpini E, De Riz M, Comi C, Venturelli E, Cortini F, Piola M, Villa C, Naldi P, Monaco F, Bresolin N, Galimberti D.

Neurosci Lett. 2007 Oct 2;425(3):173-6. Epub 2007 Aug 17.

PMID:
17825989
22.

Association of a NOS1 promoter repeat with Alzheimer's disease.

Galimberti D, Scarpini E, Venturelli E, Strobel A, Herterich S, Fenoglio C, Guidi I, Scalabrini D, Cortini F, Bresolin N, Lesch KP, Reif A.

Neurobiol Aging. 2008 Sep;29(9):1359-65. Epub 2007 Apr 6.

PMID:
17418914
23.

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.

Eur J Neurol. 2007 Apr;14(4):e3-4. No abstract available.

PMID:
17388976
24.

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.

Eur J Neurol. 2007 Feb;14(2):162-7.

PMID:
17250724
25.

Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration.

Fenoglio C, Galimberti D, Piccio L, Scalabrini D, Panina P, Buonsanti C, Venturelli E, Lovati C, Forloni G, Mariani C, Bresolin N, Scarpini E.

Neurosci Lett. 2007 Jan 10;411(2):133-7. Epub 2006 Nov 7.

PMID:
17088018
26.

Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease.

Venturelli E, Galimberti D, Fenoglio C, Lovati C, Finazzi D, Guidi I, Corrà B, Scalabrini D, Clerici F, Mariani C, Forloni G, Bresolin N, Scarpini E.

Neurosci Lett. 2006 Aug 14;404(1-2):217-21. Epub 2006 Jun 19.

PMID:
16787707
27.

Serum MCP-1 levels are increased in mild cognitive impairment and mild Alzheimer's disease.

Galimberti D, Fenoglio C, Lovati C, Venturelli E, Guidi I, Corrà B, Scalabrini D, Clerici F, Mariani C, Bresolin N, Scarpini E.

Neurobiol Aging. 2006 Dec;27(12):1763-8. Epub 2005 Nov 22.

PMID:
16307829
28.

SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis.

Fenoglio C, Galimberti D, Ban M, Maranian M, Scalabrini D, Venturelli E, Piccio L, De Riz M, Yeo TW, Goris A, Gray J, Bresolin N, Scarpini E, Compston A, Sawcer S.

Neurosci Lett. 2006 Feb 13;394(2):92-6. Epub 2005 Oct 27.

PMID:
16257118
29.

P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis.

Scalabrini D, Galimberti D, Fenoglio C, Comi C, De Riz M, Venturelli E, Castelli L, Piccio L, Ronzoni M, Lovati C, Mariani C, Monaco F, Bresolin N, Scarpini E.

Neurosci Lett. 2005 Nov 18;388(3):149-52.

PMID:
16039046
30.

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.

Neurosci Lett. 2005 Jul 15;382(3):300-3. Epub 2005 Apr 7.

PMID:
15925107
31.

Radiation hybrid mapping of two members of the Toll-like receptor gene family in pigs.

Franceschi A, Cassini P, Scalabrini D, Botti S, Bandi CM, Giuffra E.

Anim Genet. 2004 Jun;35(3):251-2. No abstract available.

PMID:
15147404
32.

VEPEMB in elderly Hodgkin's lymphoma patients. Results from an Intergruppo Italiano Linfomi (IIL) study.

Levis A, Anselmo AP, Ambrosetti A, Adamo F, Bertini M, Cavalieri E, Gavarotti P, Genua A, Liberati M, Pavone V, Pietrasanta D, Ricetti MM, Scalabrini DR, Salvi F, Vitolo U, Angelucci E, Boccadoro M, Gallo E, Mandelli F; Intergruppo Italiano Linfomi (IIL).

Ann Oncol. 2004 Jan;15(1):123-8.

PMID:
14679131

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