Mitochondrial optic neuropathies: our travels from bench to bedside and back again. - Wikidata - wikimedia - TriplyDB

Mitochondrial optic neuropathies: our travels from bench to bedside and back again.

Mitochondrial optic neuropathies: our travels from bench to bedside and back again.

http://www.wikidata.org/entity/Q38083877

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Medical management of hereditary optic neuropathies.Visual pathway neurodegeneration winged by mitochondrial dysfunction.Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways Evidence for Detrimental Cross Interactions between Reactive Oxygen and Nitrogen Species in Leber's Hereditary Optic Neuropathy Cells.A Review of Mitochondrial Optic Neuropathies: From Inherited to Acquired Forms Changes in Choroidal Thickness follow the RNFL Changes in Leber's Hereditary Optic Neuropathy Mitochondrial optic neuropathies: additional facts and concepts.Mitochondrial optic neuropathies: additional facts and concepts - response.Leber's hereditary optic neuropathy - Case report.

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Mitochondrial optic neuropathies: our travels from bench to bedside and back again.

http://www.wikidata.org/entity/Q38083877

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Mitochondrial optic neuropathies: our travels from bench to bedside and back again.

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Clinical and Experimental Ophthalmology

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Mitochondrial optic neuropathies: our travels from bench to bedside and back again

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Alfredo A Sadun

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P2860

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

Linezolid-induced optic neuropathy: a mitochondrial disorder?

The axonal transport of mitochondria

Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy

Mitochondrial dysfunction as a cause of optic neuropathies

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome

Mitochondrial disorders in the nervous system

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702-712

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scholarly article

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10.1111/CEO.12086

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7

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41

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Valerio Carelli

Chiara La Morgia

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2013-04-11T00:00:00Z

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23433229

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