Castaldo I - Search Results

1

Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients.

Vaccaro O, Lapice E, Monticelli A, Giacchetti M, Castaldo I, Galasso R, Pinelli M, Donnarumma G, Rivellese AA, Cocozza S, Riccardi G. Vaccaro O, et al. Among authors: castaldo i. Diabetes Care. 2007 May;30(5):1156-61. doi: 10.2337/dc06-1153. Epub 2007 Jan 26. Diabetes Care. 2007. PMID: 17259473

2

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

3

Recombinant human erythropoietin increases frataxin protein expression without increasing mRNA expression.

Acquaviva F, Castaldo I, Filla A, Giacchetti M, Marmolino D, Monticelli A, Pinelli M, Saccà F, Cocozza S. Acquaviva F, et al. Among authors: castaldo i. Cerebellum. 2008;7(3):360-5. doi: 10.1007/s12311-008-0036-x. Cerebellum. 2008. PMID: 18581197

4

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.

5

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

6

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.

7

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.

8

Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL).

Ragno M, Pianese L, Pinelli M, Silvestri S, Cacchiò G, Di Marzio F, Scarcella M, Coretti F, Altamura F, Monticelli A, Castaldo I. Ragno M, et al. Among authors: castaldo i. Neurogenetics. 2011 Nov;12(4):337-43. doi: 10.1007/s10048-011-0298-1. Epub 2011 Sep 1. Neurogenetics. 2011. PMID: 21881852

9

Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy.

Filla A, De Michele G, Cocozza S, Patrignani A, Volpe G, Castaldo I, Ruggiero G, Bonavita V, Masters C, Casari G, Bruni A. Filla A, et al. Among authors: castaldo i. Neurology. 2002 Mar 26;58(6):922-8. doi: 10.1212/wnl.58.6.922. Neurology. 2002. PMID: 11914409

10

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

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