Criscuolo C - Search Results

1

Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations.

Fasano D, Parisi S, Pierantoni GM, De Rosa A, Picillo M, Amodio G, Pellecchia MT, Barone P, Moltedo O, Bonifati V, De Michele G, Nitsch L, Remondelli P, Criscuolo C, Paladino S. Fasano D, et al. Among authors: criscuolo c. Cell Death Dis. 2018 Mar 7;9(3):385. doi: 10.1038/s41419-018-0410-7. Cell Death Dis. 2018. PMID: 29515184 Free PMC article.

2

Determinants of onset age in Friedreich's ataxia.

De Michele G, Filla A, Criscuolo C, Scarano V, Cavalcanti F, Pianese L, Monticelli A, Cocozza S. De Michele G, et al. Among authors: criscuolo c. J Neurol. 1998 Mar;245(3):166-8. doi: 10.1007/s004150050198. J Neurol. 1998. PMID: 9553847

3

Clinical presentation and treatment of Wilson's disease: a single-centre experience.

Pellecchia MT, Criscuolo C, Longo K, Campanella G, Filla A, Barone P. Pellecchia MT, et al. Among authors: criscuolo c. Eur Neurol. 2003;50(1):48-52. doi: 10.1159/000070858. Eur Neurol. 2003. PMID: 12824712

4

Pure unilateral hyperhidrosis after pontine infarct.

Pellecchia MT, Criscuolo C, De Joanna G, D'Amico A, Santoro L, Barone P. Pellecchia MT, et al. Among authors: criscuolo c. Neurology. 2003 Nov 11;61(9):1305. doi: 10.1212/wnl.61.9.1305. Neurology. 2003. PMID: 14610150 No abstract available.

5

Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia.

Criscuolo C, Saccà F, De Michele G, Mancini P, Combarros O, Infante J, Garcia A, Banfi S, Filla A, Berciano J. Criscuolo C, et al. Mov Disord. 2005 Oct;20(10):1358-61. doi: 10.1002/mds.20579. Mov Disord. 2005. PMID: 16007637

6

PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism.

Criscuolo C, Volpe G, De Rosa A, Varrone A, Marongiu R, Mancini P, Salvatore E, Dallapiccola B, Filla A, Valente EM, De Michele G. Criscuolo C, et al. Mov Disord. 2006 Aug;21(8):1265-7. doi: 10.1002/mds.20933. Mov Disord. 2006. PMID: 16700027

7

Nigrostriatal involvement in ataxia with oculomotor apraxia type 1.

Salvatore E, Varrone A, Criscuolo C, Mancini P, Sansone V, Strisciuglio C, Cicala D, Scarano V, Salvatore M, Pappatà S, De Michele G, Filla A. Salvatore E, et al. Among authors: criscuolo c. J Neurol. 2008 Jan;255(1):45-8. doi: 10.1007/s00415-007-0657-x. Epub 2007 Nov 21. J Neurol. 2008. PMID: 18004640

8

Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism.

Piccoli C, Ripoli M, Quarato G, Scrima R, D'Aprile A, Boffoli D, Margaglione M, Criscuolo C, De Michele G, Sardanelli A, Papa S, Capitanio N. Piccoli C, et al. Among authors: criscuolo c. J Med Genet. 2008 Sep;45(9):596-602. doi: 10.1136/jmg.2008.058628. Epub 2008 Jun 4. J Med Genet. 2008. PMID: 18524835

9

Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy.

De Rosa A, Criscuolo C, Mancini P, De Martino M, Giordano IA, Pappatà S, Filla A, De Michele G. De Rosa A, et al. Among authors: criscuolo c. Parkinsonism Relat Disord. 2009 Mar;15(3):242-4. doi: 10.1016/j.parkreldis.2008.05.011. Epub 2008 Jul 14. Parkinsonism Relat Disord. 2009. PMID: 18621566

10

Complex phenotype in an Italian family with a novel mutation in SPG3A.

de Leva MF, Filla A, Criscuolo C, Tessa A, Pappatà S, Quarantelli M, Bilo L, Peluso S, Antenora A, Longo D, Santorelli FM, De Michele G. de Leva MF, et al. Among authors: criscuolo c. J Neurol. 2010 Mar;257(3):328-31. doi: 10.1007/s00415-009-5311-3. Epub 2009 Sep 19. J Neurol. 2010. PMID: 19768483

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