Carelli V - Search Results

1

Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases.

Mancuso M, Angelini C, Bertini E, Carelli V, Comi GP, Minetti C, Moggio M, Mongini T, Servidei S, Tonin P, Toscano A, Uziel G, Zeviani M, Siciliano G; Nation-wide Italian Collaborative Network of Mitochondrial Diseases. Mancuso M, et al. Among authors: carelli v. Neuromuscul Disord. 2012 Dec;22 Suppl 3(3-3):S226-9. doi: 10.1016/j.nmd.2012.10.012. Neuromuscul Disord. 2012. PMID: 23182644 Free PMC article. Review.

2

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

3

Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation.

Carelli V, Baracca A, Barogi S, Pallotti F, Valentino ML, Montagna P, Zeviani M, Pini A, Lenaz G, Baruzzi A, Solaini G. Carelli V, et al. Arch Neurol. 2002 Feb;59(2):264-70. doi: 10.1001/archneur.59.2.264. Arch Neurol. 2002. PMID: 11843698

4

X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patients.

Pegoraro E, Vettori A, Valentino ML, Molon A, Mostacciuolo ML, Howell N, Carelli V. Pegoraro E, et al. Among authors: carelli v. Am J Med Genet A. 2003 May 15;119A(1):37-40. doi: 10.1002/ajmg.a.10211. Am J Med Genet A. 2003. PMID: 12707956

5

Nuclear genes in mitochondrial disorders.

Zeviani M, Spinazzola A, Carelli V. Zeviani M, et al. Among authors: carelli v. Curr Opin Genet Dev. 2003 Jun;13(3):262-70. doi: 10.1016/s0959-437x(03)00052-2. Curr Opin Genet Dev. 2003. PMID: 12787788 Review.

6

Mitochondrial disorders.

Zeviani M, Carelli V. Zeviani M, et al. Among authors: carelli v. Curr Opin Neurol. 2003 Oct;16(5):585-94. doi: 10.1097/01.wco.0000093101.34793.c8. Curr Opin Neurol. 2003. PMID: 14501842 Review.

7

Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case report.

Barboni P, Savini G, Plazzi G, Bellan M, Valentino ML, Zanini M, Montagna P, Hirano M, Carelli V. Barboni P, et al. Among authors: carelli v. Graefes Arch Clin Exp Ophthalmol. 2004 Oct;242(10):878-80. doi: 10.1007/s00417-004-0914-y. Epub 2004 Mar 24. Graefes Arch Clin Exp Ophthalmol. 2004. PMID: 15042378

8

Dominance in mitochondrial disorders.

Zeviani M, Carelli V. Zeviani M, et al. Among authors: carelli v. J Inherit Metab Dis. 2005;28(3):287-99. doi: 10.1007/s10545-005-0307-3. J Inherit Metab Dis. 2005. PMID: 15868464 Review.

9

The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype.

Valentino ML, Barboni P, Rengo C, Achilli A, Torroni A, Lodi R, Tonon C, Barbiroli B, Fortuna F, Montagna P, Baruzzi A, Carelli V. Valentino ML, et al. Among authors: carelli v. J Med Genet. 2006 Jul;43(7):e38. doi: 10.1136/jmg.2005.037507. J Med Genet. 2006. PMID: 16816025 Free PMC article.

10

Mitochondrial optic neuropathies: how two genomes may kill the same cell type?

Carelli V, La Morgia C, Iommarini L, Carroccia R, Mattiazzi M, Sangiorgi S, Farne' S, Maresca A, Foscarini B, Lanzi L, Amadori M, Bellan M, Valentino ML. Carelli V, et al. Biosci Rep. 2007 Jun;27(1-3):173-84. doi: 10.1007/s10540-007-9045-0. Biosci Rep. 2007. PMID: 17479363 Review.

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