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Hearing impairment in Parkinson's disease: expanding the nonmotor phenotype.
Vitale C, Marcelli V, Allocca R, Santangelo G, Riccardi P, Erro R, Amboni M, Pellecchia MT, Cozzolino A, Longo K, Picillo M, Moccia M, Agosti V, Sorrentino G, Cavaliere M, Marciano E, Barone P. Vitale C, et al. Mov Disord. 2012 Oct;27(12):1530-5. doi: 10.1002/mds.25149. Epub 2012 Oct 2. Mov Disord. 2012. PMID: 23032708
Possible gluten sensitivity in multiple system atrophy.
Pellecchia MT, Ambrosio G, Salvatore E, Vitale C, De Michele G, Barone P. Pellecchia MT, et al. Among authors: vitale c. Neurology. 2002 Oct 8;59(7):1114-5. doi: 10.1212/wnl.59.7.1114. Neurology. 2002. PMID: 12370481 No abstract available.
Cervico-oculo-Acoustic syndrome in a male with consanguineous parents.
Di Maio L, Marcelli V, Vitale C, Menzione M, De Giorgio A, Briganti F, Perretti A, Marciano E, Filla A, De Michele G. Di Maio L, et al. Among authors: vitale c. Can J Neurol Sci. 2006 May;33(2):237-9. doi: 10.1017/s0317167100005059. Can J Neurol Sci. 2006. PMID: 16736738
Apoptotic mechanisms in mutant LRRK2-mediated cell death.
Iaccarino C, Crosio C, Vitale C, Sanna G, Carrì MT, Barone P. Iaccarino C, et al. Among authors: vitale c. Hum Mol Genet. 2007 Jun 1;16(11):1319-26. doi: 10.1093/hmg/ddm080. Epub 2007 Apr 4. Hum Mol Genet. 2007. PMID: 17409193 Free article.
700 results