Carelli V - Search Results

1

Infant and Adult Gut Microbiome and Metabolome in Rural Bassa and Urban Settlers from Nigeria.

Ayeni FA, Biagi E, Rampelli S, Fiori J, Soverini M, Audu HJ, Cristino S, Caporali L, Schnorr SL, Carelli V, Brigidi P, Candela M, Turroni S. Ayeni FA, et al. Among authors: carelli v. Cell Rep. 2018 Jun 5;23(10):3056-3067. doi: 10.1016/j.celrep.2018.05.018. Cell Rep. 2018. PMID: 29874590 Free article.

2

The optic nerve: a "mito-window" on mitochondrial neurodegeneration.

Maresca A, la Morgia C, Caporali L, Valentino ML, Carelli V. Maresca A, et al. Among authors: carelli v. Mol Cell Neurosci. 2013 Jul;55(100):62-76. doi: 10.1016/j.mcn.2012.08.004. Epub 2012 Aug 15. Mol Cell Neurosci. 2013. PMID: 22960139 Free PMC article. Review.

3

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: carelli v. Neurology. 2012 Oct 2;79(14):1517-9. doi: 10.1212/WNL.0b013e31826d5f72. Epub 2012 Sep 19. Neurology. 2012. PMID: 22993283 No abstract available.

4

HPLC-UV analysis of thymidine and deoxyuridine in plasma of patients with thymidine phosphorylase deficiency.

Mohamed S, Caporali L, De Giorgio R, Carelli V, Contin M. Mohamed S, et al. Among authors: carelli v. J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Feb 15;949-950:58-62. doi: 10.1016/j.jchromb.2014.01.003. Epub 2014 Jan 8. J Chromatogr B Analyt Technol Biomed Life Sci. 2014. PMID: 24463401

5

'Behr syndrome' with OPA1 compound heterozygote mutations.

Carelli V, Sabatelli M, Carrozzo R, Rizza T, Schimpf S, Wissinger B, Zanna C, Rugolo M, La Morgia C, Caporali L, Carbonelli M, Barboni P, Tonon C, Lodi R, Bertini E. Carelli V, et al. Brain. 2015 Jan;138(Pt 1):e321. doi: 10.1093/brain/awu234. Epub 2014 Aug 21. Brain. 2015. PMID: 25146916 Free PMC article. No abstract available.

6

Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations.

Carelli V, Maresca A, Caporali L, Trifunov S, Zanna C, Rugolo M. Carelli V, et al. Int J Biochem Cell Biol. 2015 Jun;63:21-4. doi: 10.1016/j.biocel.2015.01.023. Epub 2015 Feb 7. Int J Biochem Cell Biol. 2015. PMID: 25666555 Review.

7

DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated?

Maresca A, Zaffagnini M, Caporali L, Carelli V, Zanna C. Maresca A, et al. Among authors: carelli v. Front Genet. 2015 Mar 12;6:90. doi: 10.3389/fgene.2015.00090. eCollection 2015. Front Genet. 2015. PMID: 25815005 Free PMC article.

8

ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy.

D'Angelo R, Rinaldi R, Carelli V, Boschetti E, Caporali L, Capristo M, Casali C, Cenacchi G, Gramegna LL, Lodi R, Pinna AD, Pironi L, Stanzani M, Tonon C, D'Alessandro R, De Giorgio R. D'Angelo R, et al. Among authors: carelli v. Neurol Sci. 2016 Jul;37(7):1149-51. doi: 10.1007/s10072-016-2552-7. Epub 2016 Mar 23. Neurol Sci. 2016. PMID: 27007276

9

Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction.

Santarelli R, Cama E, Scimemi P, La Morgia C, Caporali L, Valentino ML, Liguori R, Carelli V. Santarelli R, et al. Among authors: carelli v. Brain. 2016 Jun;139(Pt 6):e34. doi: 10.1093/brain/aww052. Epub 2016 Mar 25. Brain. 2016. PMID: 27016406 No abstract available.

10

Liver transplant reverses biochemical imbalance in mitochondrial neurogastrointestinal encephalomyopathy.

D'Angelo R, Rinaldi R, Pironi L, Dotti MT, Pinna AD, Boschetti E, Capristo M, Mohamed S, Contin M, Caporali L, Carelli V, De Giorgio R. D'Angelo R, et al. Among authors: carelli v. Mitochondrion. 2017 May;34:101-102. doi: 10.1016/j.mito.2017.02.006. Epub 2017 Mar 2. Mitochondrion. 2017. PMID: 28263873 No abstract available.

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