Giordano C - Search Results

1

Pantethine treatment is effective in recovering the disease phenotype induced by ketogenic diet in a pantothenate kinase-associated neurodegeneration mouse model.

Brunetti D, Dusi S, Giordano C, Lamperti C, Morbin M, Fugnanesi V, Marchet S, Fagiolari G, Sibon O, Moggio M, d'Amati G, Tiranti V. Brunetti D, et al. Among authors: giordano c. Brain. 2014 Jan;137(Pt 1):57-68. doi: 10.1093/brain/awt325. Epub 2013 Dec 6. Brain. 2014. PMID: 24316510 Free PMC article.

2

[Mitochondrial diseases].

D'Amati G, Casali C, Giordano C. D'Amati G, et al. Among authors: giordano c. Pathologica. 1999 Feb;91(1):49-50. Pathologica. 1999. PMID: 10396951 Review. Italian. No abstract available.

3

Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction.

Carelli V, Giordano C, d'Amati G. Carelli V, et al. Among authors: giordano c. Trends Genet. 2003 May;19(5):257-62. doi: 10.1016/S0168-9525(03)00072-6. Trends Genet. 2003. PMID: 12711217 Review.

4

[Cardiomyopathies due to defective energy metabolism: morphological and functional features].

Giordano C, D'Amati G. Giordano C, et al. Pathologica. 2005 Dec;97(6):361-8. Pathologica. 2005. PMID: 16619977 Review. Italian.

5

Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion.

Giordano C, Sebastiani M, De Giorgio R, Travaglini C, Tancredi A, Valentino ML, Bellan M, Cossarizza A, Hirano M, d'Amati G, Carelli V. Giordano C, et al. Am J Pathol. 2008 Oct;173(4):1120-8. doi: 10.2353/ajpath.2008.080252. Epub 2008 Sep 11. Am J Pathol. 2008. PMID: 18787099 Free PMC article.

6

Fatal congenital myopathy and gastrointestinal pseudo-obstruction due to POLG1 mutations.

Giordano C, Powell H, Leopizzi M, De Curtis M, Travaglini C, Sebastiani M, Gallo P, Taylor RW, d'Amati G. Giordano C, et al. Neurology. 2009 Mar 24;72(12):1103-5. doi: 10.1212/01.wnl.0000345002.47396.e1. Neurology. 2009. PMID: 19307547 Free PMC article. No abstract available.

7

Isolated distal myopathy of the upper limbs associated with mitochondrial DNA depletion and polymerase gamma mutations.

Giordano C, Pichiorri F, Blakely EL, Perli E, Orlandi M, Gallo P, Taylor RW, Inghilleri M, d'Amati G. Giordano C, et al. Arch Neurol. 2010 Sep;67(9):1144-6. doi: 10.1001/archneurol.2010.200. Arch Neurol. 2010. PMID: 20837862

8

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.

Giordano C, Montopoli M, Perli E, Orlandi M, Fantin M, Ross-Cisneros FN, Caparrotta L, Martinuzzi A, Ragazzi E, Ghelli A, Sadun AA, d'Amati G, Carelli V. Giordano C, et al. Brain. 2011 Jan;134(Pt 1):220-34. doi: 10.1093/brain/awq276. Epub 2010 Oct 13. Brain. 2011. PMID: 20943885 Free PMC article.

9

Evaluation of gastrointestinal mtDNA depletion in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).

Giordano C, d'Amati G. Giordano C, et al. Methods Mol Biol. 2011;755:223-32. doi: 10.1007/978-1-61779-163-5_18. Methods Mol Biol. 2011. PMID: 21761307

10

Teaching anatomical pathology in the undergraduate curriculum in medicine: the experience of 'C Course', Sapienza University, Rome.

Gallo P, D'amati G, Di Gioia C, Giordano C. Gallo P, et al. Among authors: giordano c. Pathologica. 2011 Apr;103(2):27-31. Pathologica. 2011. PMID: 21797139

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