Andreoli V - Search Results

1

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

2

Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study.

La Russa A, Cittadella R, De Marco EV, Valentino P, Andreoli V, Trecroci F, Latorre V, Gambardella A, Quattrone A. La Russa A, et al. Among authors: andreoli v. J Neuroimmunol. 2010 Aug 25;225(1-2):175-9. doi: 10.1016/j.jneuroim.2010.04.016. Epub 2010 May 14. J Neuroimmunol. 2010. PMID: 20471697

3

Presenilin enhancer-2 gene: identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease.

Andreoli V, Trecroci F, La Russa A, Cittadella R, Liguori M, Spadafora P, Caracciolo M, Di Palma G, Colica C, Gambardella A, Quattrone A. Andreoli V, et al. Alzheimers Dement. 2011 Nov;7(6):574-8. doi: 10.1016/j.jalz.2011.02.010. Alzheimers Dement. 2011. PMID: 22055974

4

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

5

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

6

Gene symbol: PSEN2. Disease: Alzheimer disease.

Andreoli V, Trecroci F, La Russa A, Di Palma G, Quattrone A, Cittadella R. Andreoli V, et al. Hum Genet. 2008 Oct;124(3):304. Hum Genet. 2008. PMID: 18846634 No abstract available.

7

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

8

CASP-9: A susceptibility locus for multiple sclerosis in Italy.

Andreoli V, Trecroci F, La Russa A, Valentino P, Condino F, Latorre V, Nisticò R, Pirritano D, Del Giudice F, Canino M, Cittadella R, Quattrone A. Andreoli V, et al. J Neuroimmunol. 2009 May 29;210(1-2):100-3. doi: 10.1016/j.jneuroim.2009.03.013. Epub 2009 Apr 8. J Neuroimmunol. 2009. PMID: 19359048

9

Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms.

Zappia M, Manna I, Serra P, Cittadella R, Andreoli V, La Russa A, Annesi F, Spadafora P, Romeo N, Nicoletti G, Messina D, Gambardella A, Quattrone A. Zappia M, et al. Among authors: andreoli v. Arch Neurol. 2004 Mar;61(3):341-4. doi: 10.1001/archneur.61.3.341. Arch Neurol. 2004. PMID: 15023809

10

A new human mtDNA polymorphism: MTND6: 14562 (C-->T).

Cittadella R, Andreoli V, Manna I, Oliveri RL, Quattrone A. Cittadella R, et al. Among authors: andreoli v. Hum Mutat. 2001 Mar;17(3):238. doi: 10.1002/humu.16. Hum Mutat. 2001. PMID: 11241853 No abstract available.

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