Caracciolo M - Search Results

1

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

2

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

3

APOE and risk of cognitive impairment in multiple sclerosis.

Oliveri RL, Cittadella R, Sibilia G, Manna I, Valentino P, Gambardella A, Aguglia U, Zappia M, Romeo N, Andreoli V, Bono F, Caracciolo M, Quattrone A. Oliveri RL, et al. Among authors: caracciolo m. Acta Neurol Scand. 1999 Nov;100(5):290-5. doi: 10.1111/j.1600-0404.1999.tb00398.x. Acta Neurol Scand. 1999. PMID: 10536914

4

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. Among authors: caracciolo m. 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.

5

A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3.

Muglia M, Magariello A, Nicoletti G, Patitucci A, Gabriele AL, Conforti FL, Mazzei R, Caracciolo M, Casari G, Ardito B, Lastilla M, Gambardella A, Quattrone A. Muglia M, et al. Among authors: caracciolo m. J Neurol. 2002 Oct;249(10):1413-6. doi: 10.1007/s00415-002-0856-4. J Neurol. 2002. PMID: 12382159

6

A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL.

Mazzei R, Conforti FL, Lanza PL, Sprovieri T, Lupo MR, Gallo O, Patitucci A, Magariello A, Caracciolo M, Gabriele AL, Fera F, Valentino P, Bono F, Cenacchi G, Santoro G, Muglia M, Quattrone A. Mazzei R, et al. Among authors: caracciolo m. Neurology. 2004 Aug 10;63(3):561-4. doi: 10.1212/01.wnl.0000133399.37716.84. Neurology. 2004. PMID: 15304596

7

Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?

Mancuso M, Conforti FL, Rocchi A, Tessitore A, Muglia M, Tedeschi G, Panza D, Monsurrò M, Sola P, Mandrioli J, Choub A, DelCorona A, Manca ML, Mazzei R, Sprovieri T, Filosto M, Salviati A, Valentino P, Bono F, Caracciolo M, Simone IL, La Bella V, Majorana G, Siciliano G, Murri L, Quattrone A. Mancuso M, et al. Among authors: caracciolo m. Neurosci Lett. 2004 Nov 23;371(2-3):158-62. doi: 10.1016/j.neulet.2004.08.060. Neurosci Lett. 2004. PMID: 15519748

8

Apolipoprotein E polymorphisms and Parkinson's disease.

Oliveri RL, Nicoletti G, Cittadella R, Manna I, Branca D, Zappia M, Gambardella A, Caracciolo M, Quattrone A. Oliveri RL, et al. Among authors: caracciolo m. Neurosci Lett. 1999 Dec 24;277(2):83-6. doi: 10.1016/s0304-3940(99)00853-8. Neurosci Lett. 1999. PMID: 10624815

9

No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case-control sample.

Nicoletti G, Annesi G, Tomaino C, Spadafora P, Pasqua AA, Annesi F, Serra P, Caracciolo M, Messina D, Zappia M, Quattrone A. Nicoletti G, et al. Among authors: caracciolo m. Neurosci Lett. 2002 Aug 2;328(1):65-7. doi: 10.1016/s0304-3940(02)00003-4. Neurosci Lett. 2002. PMID: 12123860

10

DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.

Annesi G, Savettieri G, Pugliese P, D'Amelio M, Tarantino P, Ragonese P, La Bella V, Piccoli T, Civitelli D, Annesi F, Fierro B, Piccoli F, Arabia G, Caracciolo M, Cirò Candiano IC, Quattrone A. Annesi G, et al. Among authors: caracciolo m. Ann Neurol. 2005 Nov;58(5):803-7. doi: 10.1002/ana.20666. Ann Neurol. 2005. PMID: 16240358

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