Liguori M - 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: liguori m. 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

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. Among authors: liguori m. Neurochem Res. 2007 Sep;32(9):1445-9. doi: 10.1007/s11064-007-9329-6. Epub 2007 Apr 4. Neurochem Res. 2007. PMID: 17406980

3

A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.

Liguori M, La Russa A, Manna I, Andreoli V, Caracciolo M, Spadafora P, Cittadella R, Quattrone A. Liguori M, et al. J Neurol. 2008 Jan;255(1):127-9. doi: 10.1007/s00415-008-0571-x. Epub 2008 Jan 22. J Neurol. 2008. PMID: 18204809 No abstract available.

4

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: liguori m. Alzheimers Dement. 2011 Nov;7(6):574-8. doi: 10.1016/j.jalz.2011.02.010. Alzheimers Dement. 2011. PMID: 22055974

5

Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy.

Liguori M, Tagarelli G, Romeo N, Bagalà A, Spadafora P. Liguori M, et al. Neurol Sci. 2016 Nov;37(11):1883-1885. doi: 10.1007/s10072-016-2646-2. Epub 2016 Jun 28. Neurol Sci. 2016. PMID: 27351546 No abstract available.

6

The role of VLA4 polymorphisms in multiple sclerosis: an association study.

Andreoli V, Cittadella R, Valentino P, Condino F, La Russa A, Liguori M, Manna I, Spadafora P, Nisticò R, Pirritano D, Clodomiro A, Quattrone A. Andreoli V, et al. Among authors: liguori m. J Neuroimmunol. 2007 Sep;189(1-2):125-8. doi: 10.1016/j.jneuroim.2007.06.015. Epub 2007 Jul 3. J Neuroimmunol. 2007. PMID: 17609118

7

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: liguori m. 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

8

Gene dosage influences the age at onset of SCA2 in a family from southern Italy.

Spadafora P, Annesi G, Liguori M, Tarantino P, Cutuli N, Carrideo S, Cirò Candiano IC, De Marco EV, Civitelli D, Annesi F, Giuffrida S, Quattrone A. Spadafora P, et al. Among authors: liguori m. Clin Genet. 2007 Oct;72(4):381-3. doi: 10.1111/j.1399-0004.2007.00868.x. Clin Genet. 2007. PMID: 17850638 No abstract available.

9

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. J Neurol. 2004 Feb;251(2):165-70. doi: 10.1007/s00415-004-0293-7. J Neurol. 2004. PMID: 14991350

10

Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia.

Magariello A, Muglia M, Patitucci A, Ungaro C, Mazzei R, Gabriele AL, Sprovieri T, Citrigno L, Conforti FL, Liguori M, Gambardella A, Bono F, Piccoli T, Patti F, Zappia M, Mancuso M, Iemolo F, Quattrone A. Magariello A, et al. Among authors: liguori m. J Neurol Sci. 2010 Jan 15;288(1-2):96-100. doi: 10.1016/j.jns.2009.09.025. Epub 2009 Oct 28. J Neurol Sci. 2010. PMID: 19875132

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