Criscuolo C - Search Results

1

PRICKLE1 progressive myoclonus epilepsy in Southern Italy.

Criscuolo C, de Leva MF, Sorrentino P, Piro R, Carbone R, Guacci A, De Michele G, Filla A. Criscuolo C, et al. Mov Disord. 2010 Nov 15;25(15):2686-7. doi: 10.1002/mds.23350. Mov Disord. 2010. PMID: 20842693 No abstract available.

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

Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia.

De Michele G, Cavalcanti F, Criscuolo C, Pianese L, Monticelli A, Filla A, Cocozza S. De Michele G, et al. Among authors: criscuolo c. Hum Mol Genet. 1998 Nov;7(12):1901-6. doi: 10.1093/hmg/7.12.1901. Hum Mol Genet. 1998. PMID: 9811933

4

A novel mutation in SACS gene in a family from southern Italy.

Criscuolo C, Banfi S, Orio M, Gasparini P, Monticelli A, Scarano V, Santorelli FM, Perretti A, Santoro L, De Michele G, Filla A. Criscuolo C, et al. Neurology. 2004 Jan 13;62(1):100-2. doi: 10.1212/wnl.62.1.100. Neurology. 2004. PMID: 14718706 Free article.

5

Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype.

Criscuolo C, Mancini P, Saccà F, De Michele G, Monticelli A, Santoro L, Scarano V, Banfi S, Filla A. Criscuolo C, et al. Neurology. 2004 Dec 14;63(11):2173-5. doi: 10.1212/01.wnl.0000145604.57000.36. Neurology. 2004. PMID: 15596775

6

Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation.

Coppola G, Criscuolo C, De Michele G, Striano S, Barbieri F, Striano P, Perretti A, Santoro L, Brescia Morra V, Saccà F, Scarano V, D'Adamo AP, Banfi S, Gasparini P, Santorelli FM, Lehesjoki AE, Filla A. Coppola G, et al. Among authors: criscuolo c. J Neurol. 2005 Aug;252(8):897-900. doi: 10.1007/s00415-005-0766-3. Epub 2005 Mar 8. J Neurol. 2005. PMID: 15742102

7

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

8

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

9

Screening for POLG1 mutations in a Southern Italian ataxia population.

Criscuolo C, Mancini P, Ammendola S, Cicala D, Banfi S, De Michele G, Filla A. Criscuolo C, et al. J Neurol. 2008 Mar;255(3):454-5. doi: 10.1007/s00415-007-0736-z. Epub 2007 Dec 19. J Neurol. 2008. PMID: 18080848 No abstract available.

10

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

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