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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 3
2004 3
2007 1
2008 2
2010 2
2011 3
2012 1
2013 1
2014 1
2017 1
2021 0
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18 results
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Page 1
Genetic Aspects of Susceptibility to Mercury Toxicity: An Overview.
Andreoli V, Sprovieri F. Andreoli V, et al. Int J Environ Res Public Health. 2017 Jan 18;14(1):93. doi: 10.3390/ijerph14010093. Int J Environ Res Public Health. 2017. PMID: 28106810 Free PMC article. Review.
CAV3 T78M mutation as polymorphic variant in South Italy.
Spadafora P, Liguori M, Andreoli V, Quattrone A, Gambardella A. Spadafora P, et al. Among authors: andreoli v. Neuromuscul Disord. 2012 Jul;22(7):669-70; author reply 670-1. doi: 10.1016/j.nmd.2012.03.007. Epub 2012 May 16. Neuromuscul Disord. 2012. PMID: 22595201 No abstract available.
Presenilin-2 gene mutation presenting as Lewy body dementia?
Raciti L, Nicoletti A, Le Pira F, Andreoli V, Contrafatto D, Lanzafame S, Maci T, Gambardella A, Quattrone A, Zappia M. Raciti L, et al. Among authors: andreoli v. Neurol Sci. 2011 Jun;32(3):533-4. doi: 10.1007/s10072-011-0497-4. Epub 2011 Mar 16. Neurol Sci. 2011. PMID: 21409510 No abstract available.
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy.
Gambardella A, Manna I, Labate A, Chifari R, Serra P, La Russa A, LePiane E, Cittadella R, Andreoli V, Sasanelli F, Zappia M, Aguglia U, Quattrone A. Gambardella A, et al. Among authors: andreoli v. Epilepsia. 2003 Sep;44(9):1255-6. doi: 10.1046/j.1528-1157.2003.18003.x. Epilepsia. 2003. PMID: 12919401 Free article. No abstract available.
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease.
Andreoli V, De Marco EV, Trecroci F, Cittadella R, Di Palma G, Gambardella A. Andreoli V, et al. J Neural Transm (Vienna). 2014 May;121(5):533-42. doi: 10.1007/s00702-013-1125-7. Epub 2013 Dec 1. J Neural Transm (Vienna). 2014. PMID: 24292895
Lack of interaction between LRP1 and A2M polymorphisms for the risk of Alzheimer disease.
Bruno E, Quattrocchi G, Nicoletti A, Le Pira F, Maci T, Mostile G, Andreoli V, Quattrone A, Zappia M. Bruno E, et al. Among authors: andreoli v. Neurosci Lett. 2010 Sep 27;482(2):112-6. doi: 10.1016/j.neulet.2010.07.012. Epub 2010 Jul 14. Neurosci Lett. 2010. PMID: 20637261
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis.
Liguori M, Cittadella R, Manna I, Valentino P, La Russa A, Serra P, Trojano M, Messina D, Ruscica F, Andreoli V, Romeo N, Livrea P, Quattrone A. Liguori M, et al. Among authors: andreoli v. J Neurol. 2004 Feb;251(2):165-70. doi: 10.1007/s00415-004-0293-7. J Neurol. 2004. PMID: 14991350
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.
La Russa A, Cittadella R, Andreoli V, Valentino P, Trecroci F, Caracciolo M, Gallo O, Gambardella A, Quattrone A. La Russa A, et al. Among authors: andreoli v. Mult Scler. 2011 Jun;17(6):763-6. doi: 10.1177/1352458511404033. Mult Scler. 2011. PMID: 21685233
Fas antigen and sporadic Alzheimer's disease in Southern Italy: evaluation of two polymorphisms in the TNFRSF6 gene.
Andreoli V, Nicoletti G, Romeo N, Condino F, La Russa A, Liguori M, Manna I, Spadafora P, Quattrone A, Cittadella R. Andreoli V, et al. Neurochem Res. 2007 Sep;32(9):1445-9. doi: 10.1007/s11064-007-9329-6. Epub 2007 Apr 4. Neurochem Res. 2007. PMID: 17406980
Gender-related effect of clinical and genetic variables on the cognitive impairment in multiple sclerosis.
Savettieri G, Messina D, Andreoli V, Bonavita S, Caltagirone C, Cittadella R, Farina D, Fazio MC, Girlanda P, Le Pira F, Liguori M, Lugaresi A, Nocentini U, Reggio A, Salemi G, Tedeschi G, Trojano M, Valentino P, Quattrone A. Savettieri G, et al. Among authors: andreoli v. J Neurol. 2004 Oct;251(10):1208-14. doi: 10.1007/s00415-004-0508-y. J Neurol. 2004. PMID: 15503099
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