Leber hereditary optic neuropathy: bridging the translational gap.

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Pluripotent Stem Cell-Based Approaches to Explore and Treat Optic Neuropathies Principles of OCTA and Applications in Clinical Neurology

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Leber hereditary optic neuropathy: bridging the translational gap.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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name

Leber hereditary optic neuropathy: bridging the translational gap.

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Leber hereditary optic neuropathy: bridging the translational gap.

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Leber hereditary optic neuropathy: bridging the translational gap.

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Leber hereditary optic neuropathy: bridging the translational gap.

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Leber hereditary optic neuropathy: bridging the translational gap.

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Leber hereditary optic neuropathy: bridging the translational gap.

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P1476

Leber hereditary optic neuropathy: bridging the translational gap.

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Neringa Jurkute

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Patrick Yu-Wai-Man

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Creative Commons Attribution 4.0 International

P2860

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder

Allotopic expression of mitochondrial-encoded genes in mammals: achieved goal, undemonstrated mechanism or impossible task?

The epidemiology of Leber hereditary optic neuropathy in the North East of England

Genetic manipulation for inherited neurodegenerative diseases: myth or reality?

A neurodegenerative perspective on mitochondrial optic neuropathies

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

Towards clinical application of pronuclear transfer to prevent mitochondrial DNA disease.

Natural history of Leber's hereditary optic neuropathy: longitudinal analysis of the retinal nerve fiber layer by optical coherence tomography.

Treatment strategies for inherited optic neuropathies: past, present and future

Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy

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403-409

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10.1097/ICU.0000000000000410

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2017-06-24T00:00:00Z

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2017-09-01T00:00:00Z

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sensory system

Leber hereditary optic neuropathy

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Leber hereditary optic neuropathy: bridging the translational gap.

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P2860

P2860

Leber hereditary optic neuropathy: bridging the translational gap.

description

name

type

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P1433

P1476

P2093

P275

P2860

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P356

P1433

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P356

P433

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P921

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