Castaldo I - Search Results

1

Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.

Pianese L, Cocozza S, Campanella G, Castaldo I, Cavalcanti F, De Michele G, Filla A, Monticelli A, Munaro M, Redolfi E, et al. Pianese L, et al. Among authors: castaldo i. J Med Genet. 1994 Feb;31(2):133-5. doi: 10.1136/jmg.31.2.133. J Med Genet. 1994. PMID: 8182719 Free PMC article.

2

Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.

De Michele G, Filla A, Cavalcanti F, Di Maio L, Pianese L, Castaldo I, Calabrese O, Monticelli A, Varrone S, Campanella G, et al. De Michele G, et al. Among authors: castaldo i. J Neurol Neurosurg Psychiatry. 1994 Aug;57(8):977-9. doi: 10.1136/jnnp.57.8.977. J Neurol Neurosurg Psychiatry. 1994. PMID: 8057123 Free PMC article.

3

DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients.

Castaldo I, Pinelli M, Monticelli A, Acquaviva F, Giacchetti M, Filla A, Sacchetti S, Keller S, Avvedimento VE, Chiariotti L, Cocozza S. Castaldo I, et al. J Med Genet. 2008 Dec;45(12):808-12. doi: 10.1136/jmg.2008.058594. Epub 2008 Aug 12. J Med Genet. 2008. PMID: 18697824

4

Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.

Filla A, De Michele G, Banfi S, Santoro L, Perretti A, Cavalcanti F, Pianese L, Castaldo I, Barbieri F, Campanella G, et al. Filla A, et al. Among authors: castaldo i. Neurology. 1995 Apr;45(4):793-6. doi: 10.1212/wnl.45.4.793. Neurology. 1995. PMID: 7723972

5

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes.

Filla A, De Michele G, Campanella G, Perretti A, Santoro L, Serlenga L, Ragno M, Calabrese O, Castaldo I, De Joanna G, Cocozza S. Filla A, et al. Among authors: castaldo i. J Neurol Sci. 1996 Oct;142(1-2):140-7. doi: 10.1016/0022-510x(96)00177-3. J Neurol Sci. 1996. PMID: 8902734

6

Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families.

Filla A, De Michele G, Santoro L, Calabrese O, Castaldo I, Giuffrida S, Restivo D, Serlenga L, Condorelli DF, Bonuccelli U, Scala R, Coppola G, Caruso G, Cocozza S. Filla A, et al. Among authors: castaldo i. J Neurol. 1999 Jun;246(6):467-71. doi: 10.1007/s004150050385. J Neurol. 1999. PMID: 10431773

7

Can telomere shortening in human peripheral blood leukocytes serve as a disease biomarker of Friedreich's ataxia?

Castaldo I, Vergara P, Pinelli M, Filla A, De Michele G, Cocozza S, Monticelli A. Castaldo I, et al. Antioxid Redox Signal. 2013 Apr 10;18(11):1303-6. doi: 10.1089/ars.2012.5009. Epub 2012 Dec 13. Antioxid Redox Signal. 2013. PMID: 23146029 Free PMC article.

8

The effect of parental gender on the GAA dynamic mutation in the FRDA gene.

Pianese L, Cavalcanti F, De Michele G, Filla A, Campanella G, Calabrese O, Castaldo I, Monticelli A, Cocozza S. Pianese L, et al. Among authors: castaldo i. Am J Hum Genet. 1997 Feb;60(2):460-3. Am J Hum Genet. 1997. PMID: 9012421 Free PMC article. No abstract available.

9

PPAR-gamma agonist Azelaoyl PAF increases frataxin protein and mRNA expression: new implications for the Friedreich's ataxia therapy.

Marmolino D, Acquaviva F, Pinelli M, Monticelli A, Castaldo I, Filla A, Cocozza S. Marmolino D, et al. Among authors: castaldo i. Cerebellum. 2009 Jun;8(2):98-103. doi: 10.1007/s12311-008-0087-z. Epub 2008 Dec 23. Cerebellum. 2009. PMID: 19104905

10

A distinct group of CpG islands shows differential DNA methylation between replicas of the same cell line in vitro.

Cocozza S, Scala G, Miele G, Castaldo I, Monticelli A. Cocozza S, et al. Among authors: castaldo i. BMC Genomics. 2013 Oct 10;14:692. doi: 10.1186/1471-2164-14-692. BMC Genomics. 2013. PMID: 24106769 Free PMC article.

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