Prelle A - Search Results

1

Increased longevity and refractoriness to Ca(2+)-dependent neurodegeneration in Surf1 knockout mice.

Dell'agnello C, Leo S, Agostino A, Szabadkai G, Tiveron C, Zulian A, Prelle A, Roubertoux P, Rizzuto R, Zeviani M. Dell'agnello C, et al. Among authors: prelle a. Hum Mol Genet. 2007 Feb 15;16(4):431-44. doi: 10.1093/hmg/ddl477. Epub 2007 Jan 8. Hum Mol Genet. 2007. PMID: 17210671

2

Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice.

Agostino A, Invernizzi F, Tiveron C, Fagiolari G, Prelle A, Lamantea E, Giavazzi A, Battaglia G, Tatangelo L, Tiranti V, Zeviani M. Agostino A, et al. Among authors: prelle a. Hum Mol Genet. 2003 Feb 15;12(4):399-413. doi: 10.1093/hmg/ddg038. Hum Mol Genet. 2003. PMID: 12566387

3

Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy.

Tiranti V, Viscomi C, Hildebrandt T, Di Meo I, Mineri R, Tiveron C, Levitt MD, Prelle A, Fagiolari G, Rimoldi M, Zeviani M. Tiranti V, et al. Among authors: prelle a. Nat Med. 2009 Feb;15(2):200-5. doi: 10.1038/nm.1907. Epub 2009 Jan 11. Nat Med. 2009. PMID: 19136963

4

Chronic exposure to sulfide causes accelerated degradation of cytochrome c oxidase in ethylmalonic encephalopathy.

Di Meo I, Fagiolari G, Prelle A, Viscomi C, Zeviani M, Tiranti V. Di Meo I, et al. Among authors: prelle a. Antioxid Redox Signal. 2011 Jul 15;15(2):353-62. doi: 10.1089/ars.2010.3520. Epub 2011 Feb 25. Antioxid Redox Signal. 2011. PMID: 20812865

5

Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study.

Mariotti C, Uziel G, Carrara F, Mora M, Prelle A, Tiranti V, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: prelle a. J Neurol. 1995 Sep;242(9):547-56. doi: 10.1007/BF00868806. J Neurol. 1995. PMID: 8551315

6

OXPHOS defects and mitochondrial DNA mutations in cardiomyopathy.

Zeviani M, Mariotti C, Antozzi C, Fratta GM, Rustin P, Prelle A. Zeviani M, et al. Among authors: prelle a. Muscle Nerve Suppl. 1995;3:S170-4. doi: 10.1002/mus.880181433. Muscle Nerve Suppl. 1995. PMID: 7603520

7

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

Comi GP, Bordoni A, Salani S, Franceschina L, Sciacco M, Prelle A, Fortunato F, Zeviani M, Napoli L, Bresolin N, Moggio M, Ausenda CD, Taanman JW, Scarlato G. Comi GP, et al. Among authors: prelle a. Ann Neurol. 1998 Jan;43(1):110-6. doi: 10.1002/ana.410430119. Ann Neurol. 1998. PMID: 9450776

8

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA.

Mariotti C, Savarese N, Suomalainen A, Rimoldi M, Comi G, Prelle A, Antozzi C, Servidei S, Jarre L, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: prelle a. J Neurol. 1995 May;242(5):304-12. doi: 10.1007/BF00878873. J Neurol. 1995. PMID: 7643139

9

Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level.

Prelle A, Fagiolari G, Checcarelli N, Moggio M, Battistel A, Comi GP, Bazzi P, Bordoni A, Zeviani M, Scarlato G. Prelle A, et al. Acta Neuropathol. 1994;87(4):371-6. doi: 10.1007/BF00313606. Acta Neuropathol. 1994. PMID: 8017172

10

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.

Zeviani M, Gellera C, Pannacci M, Uziel G, Prelle A, Servidei S, DiDonato S. Zeviani M, et al. Among authors: prelle a. Ann Neurol. 1990 Jul;28(1):94-7. doi: 10.1002/ana.410280118. Ann Neurol. 1990. PMID: 2375642

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