Carelli V - Search Results

1

Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines.

Beretta S, Mattavelli L, Sala G, Tremolizzo L, Schapira AH, Martinuzzi A, Carelli V, Ferrarese C. Beretta S, et al. Among authors: carelli v. Brain. 2004 Oct;127(Pt 10):2183-92. doi: 10.1093/brain/awh258. Epub 2004 Sep 1. Brain. 2004. PMID: 15342361

2

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

Vergani L, Martinuzzi A, Carelli V, Cortelli P, Montagna P, Schievano G, Carrozzo R, Angelini C, Lugaresi E. Vergani L, et al. Among authors: carelli v. Biochem Biophys Res Commun. 1995 May 25;210(3):880-8. doi: 10.1006/bbrc.1995.1740. Biochem Biophys Res Commun. 1995. PMID: 7763260

3

Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy.

Degli Esposti M, Carelli V, Ghelli A, Ratta M, Crimi M, Sangiorgi S, Montagna P, Lenaz G, Lugaresi E, Cortelli P. Degli Esposti M, et al. Among authors: carelli v. FEBS Lett. 1994 Oct 3;352(3):375-9. doi: 10.1016/0014-5793(94)00971-6. FEBS Lett. 1994. PMID: 7926004 Free article.

4

Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype.

Carelli V, Ghelli A, Ratta M, Bacchilega E, Sangiorgi S, Mancini R, Leuzzi V, Cortelli P, Montagna P, Lugaresi E, Degli Esposti M. Carelli V, et al. Neurology. 1997 Jun;48(6):1623-32. doi: 10.1212/wnl.48.6.1623. Neurology. 1997. PMID: 9191778

5

Changes in mitochondrial complex I activity and coenzyme Q binding site in Leber's hereditary optic neuropathy (LHON).

Ghelli A, Degli Esposti M, Carelli V, Lenaz G. Ghelli A, et al. Among authors: carelli v. Mol Aspects Med. 1997;18 Suppl:S263-7. doi: 10.1016/s0098-2997(97)00028-9. Mol Aspects Med. 1997. PMID: 9266534

6

Childhood Leber's hereditary optic neuropathy (ND1/3460) with visual recovery.

Pezzi PP, De Negri AM, Sadun F, Carelli V, Leuzzi V. Pezzi PP, et al. Among authors: carelli v. Pediatr Neurol. 1998 Oct;19(4):308-12. doi: 10.1016/s0887-8994(98)00060-5. Pediatr Neurol. 1998. PMID: 9831004

7

Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy.

Carelli V, Ghelli A, Bucchi L, Montagna P, De Negri A, Leuzzi V, Carducci C, Lenaz G, Lugaresi E, Degli Esposti M. Carelli V, et al. Ann Neurol. 1999 Mar;45(3):320-8. Ann Neurol. 1999. PMID: 10072046

8

'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation.

Lodi R, Montagna P, Cortelli P, Iotti S, Cevoli S, Carelli V, Barbiroli B. Lodi R, et al. Among authors: carelli v. Brain. 2000 Sep;123 ( Pt 9):1896-902. doi: 10.1093/brain/123.9.1896. Brain. 2000. PMID: 10960053

9

Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis.

Danielson SR, Wong A, Carelli V, Martinuzzi A, Schapira AH, Cortopassi GA. Danielson SR, et al. Among authors: carelli v. J Biol Chem. 2002 Feb 22;277(8):5810-5. doi: 10.1074/jbc.M110119200. Epub 2001 Dec 11. J Biol Chem. 2002. PMID: 11741983 Free article.

10

Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy.

Lodi R, Carelli V, Cortelli P, Iotti S, Valentino ML, Barboni P, Pallotti F, Montagna P, Barbiroli B. Lodi R, et al. Among authors: carelli v. J Neurol Neurosurg Psychiatry. 2002 Jun;72(6):805-7. doi: 10.1136/jnnp.72.6.805. J Neurol Neurosurg Psychiatry. 2002. PMID: 12023431 Free PMC article.

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