Carelli V - Search Results

1

International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy.

Carelli V, Carbonelli M, de Coo IF, Kawasaki A, Klopstock T, Lagrèze WA, La Morgia C, Newman NJ, Orssaud C, Pott JWR, Sadun AA, van Everdingen J, Vignal-Clermont C, Votruba M, Yu-Wai-Man P, Barboni P. Carelli V, et al. J Neuroophthalmol. 2017 Dec;37(4):371-381. doi: 10.1097/WNO.0000000000000570. J Neuroophthalmol. 2017. PMID: 28991104

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

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.

4

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

5

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

6

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.

7

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

8

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.

9

Optic neuropathy in Lhon and Leigh syndrome.

Carelli V, Sadun AA. Carelli V, et al. Ophthalmology. 2001 Jul;108(7):1172-3. doi: 10.1016/s0161-6420(01)00618-2. Ophthalmology. 2001. PMID: 11425664 No abstract available.

10

Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases.

Carelli V, Valentino ML, Liguori R, Meletti S, Vetrugno R, Provini F, Mancardi GL, Bandini F, Baruzzi A, Montagna P. Carelli V, et al. J Neurol Neurosurg Psychiatry. 2001 Dec;71(6):813-6. doi: 10.1136/jnnp.71.6.813. J Neurol Neurosurg Psychiatry. 2001. PMID: 11723211 Free PMC article.

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