Carelli V - Search Results

1

Changes in Choroidal Thickness follow the RNFL Changes in Leber's Hereditary Optic Neuropathy.

Borrelli E, Triolo G, Cascavilla ML, La Morgia C, Rizzo G, Savini G, Balducci N, Nucci P, Giglio R, Darvizeh F, Parisi V, Bandello F, Sadun AA, Carelli V, Barboni P. Borrelli E, et al. Among authors: carelli v. Sci Rep. 2016 Nov 17;6:37332. doi: 10.1038/srep37332. Sci Rep. 2016. PMID: 27853297 Free PMC article.

2

Abnormal lactate after effort in healthy carriers of Leber's hereditary optic neuropathy.

Montagna P, Plazzi G, Cortelli P, Carelli V, Lugaresi E, Barboni P, Fiocchi M. Montagna P, et al. Among authors: carelli v. J Neurol Neurosurg Psychiatry. 1995 May;58(5):640-1. doi: 10.1136/jnnp.58.5.640. J Neurol Neurosurg Psychiatry. 1995. PMID: 7745422 Free PMC article. No abstract available.

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

Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy.

Torroni A, Carelli V, Petrozzi M, Terracina M, Barboni P, Malpassi P, Wallace DC, Scozzari R. Torroni A, et al. Among authors: carelli v. Am J Hum Genet. 1996 Jul;59(1):248-52. Am J Hum Genet. 1996. PMID: 8659531 Free PMC article. No abstract available.

5

X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant.

Pegoraro E, Carelli V, Zeviani M, Cortelli P, Montagna P, Barboni P, Angelini C, Hoffman EP. Pegoraro E, et al. Among authors: carelli v. Am J Med Genet. 1996 Feb 2;61(4):356-62. doi: 10.1002/(SICI)1096-8628(19960202)61:4<356::AID-AJMG10>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8834048

6

Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS study.

Cortelli P, Montagna P, Pierangeli G, Lodi R, Barboni P, Liguori R, Carelli V, Iotti S, Zaniol P, Lugaresi E, Barbiroli B. Cortelli P, et al. Among authors: carelli v. J Neurol Sci. 1997 May 1;148(1):25-31. doi: 10.1016/s0022-510x(96)00311-5. J Neurol Sci. 1997. PMID: 9125387

7

Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

Torroni A, Petrozzi M, D'Urbano L, Sellitto D, Zeviani M, Carrara F, Carducci C, Leuzzi V, Carelli V, Barboni P, De Negri A, Scozzari R. Torroni A, et al. Among authors: carelli v. Am J Hum Genet. 1997 May;60(5):1107-21. Am J Hum Genet. 1997. PMID: 9150158 Free PMC article.

8

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient.

Carelli V, Barboni P, Zacchini A, Mancini R, Monari L, Cevoli S, Liguori R, Sensi M, Lugaresi E, Montagna P. Carelli V, et al. J Neurol Sci. 1998 Oct 8;160(2):183-8. doi: 10.1016/s0022-510x(98)00239-1. J Neurol Sci. 1998. PMID: 9849804

9

Congenital encephalomyopathy with epilepsy, chorioretinitis, basal ganglia involvement, and muscle minicores.

Avoni P, Monari L, Carelli V, Carcangiu R, Barboni P, Donati C, Badiali L, Baruzzi A, Montagna P. Avoni P, et al. Among authors: carelli v. Ann Neurol. 2000 Mar;47(3):395-9. Ann Neurol. 2000. PMID: 10716265

10

Leber's hereditary optic neuropathy differentially affects smaller axons in the optic nerve.

Sadun AA, Win PH, Ross-Cisneros FN, Walker SO, Carelli V. Sadun AA, et al. Among authors: carelli v. Trans Am Ophthalmol Soc. 2000;98:223-32; discussion 232-5. Trans Am Ophthalmol Soc. 2000. PMID: 11190025 Free PMC article.

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