Giordano C - Search Results

1

Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies.

Iommarini L, Maresca A, Caporali L, Valentino ML, Liguori R, Giordano C, Carelli V. Iommarini L, et al. Among authors: giordano c. Neurology. 2012 Oct 2;79(14):1517-9. doi: 10.1212/WNL.0b013e31826d5f72. Epub 2012 Sep 19. Neurology. 2012. PMID: 22993283 No abstract available.

2

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.

3

Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine.

Giordano C, Sebastiani M, Plazzi G, Travaglini C, Sale P, Pinti M, Tancredi A, Liguori R, Montagna P, Bellan M, Valentino ML, Cossarizza A, Hirano M, d'Amati G, Carelli V. Giordano C, et al. Gastroenterology. 2006 Mar;130(3):893-901. doi: 10.1053/j.gastro.2006.01.004. Gastroenterology. 2006. PMID: 16530527

4

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.

5

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.

6

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.

7

Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number.

Marucci G, Maresca A, Caporali L, Farnedi A, Betts CM, Morandi L, de Biase D, Cerasoli S, Foschini MP, Bonora E, Vidone M, Romeo G, Perli E, Giordano C, d'Amati G, Gasparre G, Baruzzi A, Carelli V, Eusebi V. Marucci G, et al. Among authors: giordano c. Hum Pathol. 2013 Sep;44(9):1867-76. doi: 10.1016/j.humpath.2013.02.014. Epub 2013 May 9. Hum Pathol. 2013. PMID: 23664543

8

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.

Giordano C, Iommarini L, Giordano L, Maresca A, Pisano A, Valentino ML, Caporali L, Liguori R, Deceglie S, Roberti M, Fanelli F, Fracasso F, Ross-Cisneros FN, D'Adamo P, Hudson G, Pyle A, Yu-Wai-Man P, Chinnery PF, Zeviani M, Salomao SR, Berezovsky A, Belfort R Jr, Ventura DF, Moraes M, Moraes Filho M, Barboni P, Sadun F, De Negri A, Sadun AA, Tancredi A, Mancini M, d'Amati G, Loguercio Polosa P, Cantatore P, Carelli V. Giordano C, et al. Among authors: giordano l. Brain. 2014 Feb;137(Pt 2):335-53. doi: 10.1093/brain/awt343. Epub 2013 Dec 24. Brain. 2014. PMID: 24369379 Free PMC article.

9

Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy.

Pippucci T, Maresca A, Magini P, Cenacchi G, Donadio V, Palombo F, Papa V, Incensi A, Gasparre G, Valentino ML, Preziuso C, Pisano A, Ragno M, Liguori R, Giordano C, Tonon C, Lodi R, Parmeggiani A, Carelli V, Seri M. Pippucci T, et al. Among authors: giordano c. EMBO Mol Med. 2015 Jun;7(6):848-58. doi: 10.15252/emmm.201404399. EMBO Mol Med. 2015. PMID: 25870235 Free PMC article.

10

Reply: Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers.

Giordano C, Carelli V. Giordano C, et al. Brain. 2016 Jan;139(Pt 1):e2. doi: 10.1093/brain/awv217. Epub 2015 Jul 23. Brain. 2016. PMID: 26209316 Free PMC article. No abstract available.

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