Idebenone treatment in patients with OPA1-mutant dominant optic atrophy-Reference-Cited by-同舟云学术

Idebenone treatment in patients with OPA1-mutant dominant optic atrophy

Published:2013-02 Issue:2 Volume:136 Page:e231-e231
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Barboni Piero,Valentino Maria Lucia,La Morgia Chiara,Carbonelli Michele,Savini Giacomo,De Negri Annamaria,Simonelli Francesca,Sadun Federico,Caporali Leonardo,Maresca Alessandra,Liguori Rocco,Baruzzi Agostino,Zeviani Massimo,Carelli Valerio

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/136/2/e231/11137184/aws280.pdf

Reference20 articles.

1. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to choromosome 3q28;Alexander;Nat Genet,2000

2. OPA1 mutations associated with dominant optic atrophy influence optic nerve head size;Barboni;Ophthalmology,2010

3. Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders;Carelli;Biochim Biophys Acta,2009

4. Idebenone treatment in Leber’s hereditary optic neuropathy;Carelli;Brain,2011

5. Mitochondrial dysfunction as a cause of optic neuropathies;Carelli;Prog Ret Eye Res,2004

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