Gambardella A - Search Results

1

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: gambardella a. 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.

2

Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia.

Magariello A, Muglia M, Patitucci A, Mazzei R, Conforti FL, Gabriele AL, Sprovieri T, Ungaro C, Gambardella A, Mancuso M, Siciliano G, Branca D, Aguglia U, de Angelis MV, Longo K, Quattrone A. Magariello A, et al. Among authors: gambardella a. Neuromuscul Disord. 2006 Jun;16(6):387-90. doi: 10.1016/j.nmd.2006.03.009. Epub 2006 May 8. Neuromuscul Disord. 2006. PMID: 16684598

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. Among authors: gambardella a. Alzheimers Dement. 2011 Nov;7(6):574-8. doi: 10.1016/j.jalz.2011.02.010. Alzheimers Dement. 2011. PMID: 22055974

4

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: gambardella a. 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.

5

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: gambardella a. Arch Neurol. 2004 Mar;61(3):341-4. doi: 10.1001/archneur.61.3.341. Arch Neurol. 2004. PMID: 15023809

6

NOS2A as a candidate gene in Relapsing-Remitting Multiple Sclerosis: a haplotype study using selected subsets of single nucleotide polymorphisms.

Manna I, Liguori M, Valentino P, Vena L, Condino F, Nisticò R, Di Palma G, Quattrone A, Gambardella A. Manna I, et al. Among authors: gambardella a. J Neurol Sci. 2011 May 15;304(1-2):75-7. doi: 10.1016/j.jns.2011.02.008. Epub 2011 Mar 3. J Neurol Sci. 2011. PMID: 21376344

7

Septo-optic dysplasia plus bilateral perisylvian polymicrogyria: a case report.

Labate A, Gambardella A, Quattrone A. Labate A, et al. Among authors: gambardella a. Neurol Sci. 2013 Aug;34(8):1479-80. doi: 10.1007/s10072-012-1227-2. Epub 2012 Nov 4. Neurol Sci. 2013. PMID: 23124487 No abstract available.

8

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: gambardella a. Mult Scler. 2011 Jun;17(6):763-6. doi: 10.1177/1352458511404033. Mult Scler. 2011. PMID: 21685233

9

Treatment of palatal myoclonus with sumatriptan.

Gambardella A, Quattrone A. Gambardella A, et al. Mov Disord. 1998 Jan;13(1):195. doi: 10.1002/mds.870130145. Mov Disord. 1998. PMID: 9452358 No abstract available.

10

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: gambardella a. 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

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