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Page 1
Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis.
Giacalone G, Clarelli F, Osiceanu AM, Guaschino C, Brambilla P, Sorosina M, Liberatore G, Zauli A, Esposito F, Rodegher M, Ghezzi A, Galimberti D, Patti F, Barizzone N, Guerini F, Martinelli V, Leone M, Comi G, D'Alfonso S, Martinelli Boneschi F. Giacalone G, et al. Among authors: galimberti d, d alfonso s. Mult Scler. 2015 Oct;21(11):1431-42. doi: 10.1177/1352458514564590. Epub 2015 Jan 12. Mult Scler. 2015. PMID: 25583839
Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients.
Guidi I, Galimberti D, Venturelli E, Lovati C, Del Bo R, Fenoglio C, Gatti A, Dominici R, Galbiati S, Virgilio R, Pomati S, Comi GP, Mariani C, Forloni G, Bresolin N, Scarpini E. Guidi I, et al. Among authors: galimberti d. Neurobiol Aging. 2005 Jun;26(6):789-94. doi: 10.1016/j.neurobiolaging.2004.07.003. Neurobiol Aging. 2005. PMID: 15718036 Clinical Trial.
Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis.
Del Bo R, Scarlato M, Ghezzi S, Martinelli-Boneschi F, Fenoglio C, Galimberti G, Galbiati S, Virgilio R, Galimberti D, Ferrarese C, Scarpini E, Bresolin N, Comi GP. Del Bo R, et al. Among authors: galimberti g, galimberti d. Neurobiol Aging. 2006 May;27(5):770.e1-770.e5. doi: 10.1016/j.neurobiolaging.2005.05.025. Epub 2005 Aug 15. Neurobiol Aging. 2006. PMID: 16099550
ICOS gene haplotypes correlate with IL10 secretion and multiple sclerosis evolution.
Castelli L, Comi C, Chiocchetti A, Nicola S, Mesturini R, Giordano M, D'Alfonso S, Cerutti E, Galimberti D, Fenoglio C, Tesser F, Yagi J, Rojo JM, Perla F, Leone M, Scarpini E, Monaco F, Dianzani U. Castelli L, et al. Among authors: galimberti d, d alfonso s. J Neuroimmunol. 2007 May;186(1-2):193-8. doi: 10.1016/j.jneuroim.2007.03.022. Epub 2007 May 3. J Neuroimmunol. 2007. PMID: 17481737
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy.
D'Alfonso S, Bolognesi E, Guerini FR, Barizzone N, Bocca S, Ferrante D, Castelli L, Bergamaschi L, Agliardi C, Ferrante P, Naldi P, Leone M, Caputo D, Ballerini C, Salvetti M, Galimberti D, Massacesi L, Trojano M, Momigliano-Richiardi P. D'Alfonso S, et al. Among authors: galimberti d. Genes Immun. 2008 Jan;9(1):7-15. doi: 10.1038/sj.gene.6364437. Epub 2007 Oct 11. Genes Immun. 2008. PMID: 17928868
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. Galimberti D, et al. Mult Scler. 2008 May;14(4):547-9. doi: 10.1177/1352458507084268. Epub 2008 Jan 21. Mult Scler. 2008. PMID: 18208895
Variations of the perforin gene in patients with multiple sclerosis.
Cappellano G, Orilieri E, Comi C, Chiocchetti A, Bocca S, Boggio E, Bernardone IS, Cometa A, Clementi R, Barizzone N, D'Alfonso S, Corrado L, Galimberti D, Scarpini E, Guerini FR, Caputo D, Paolicelli D, Trojano M, Figà-Talamanca L, Salvetti M, Perla F, Leone M, Monaco F, Dianzani U. Cappellano G, et al. Among authors: galimberti d, d alfonso s. Genes Immun. 2008 Jul;9(5):438-44. doi: 10.1038/gene.2008.35. Epub 2008 May 22. Genes Immun. 2008. PMID: 18496551
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. Villa C, et al. Among authors: galimberti d. Eur J Neurol. 2009 Jul;16(7):870-3. doi: 10.1111/j.1468-1331.2009.02611.x. Epub 2009 Mar 31. Eur J Neurol. 2009. PMID: 19473369
619 results