Leber’s Hereditary Optic Neuropathy as a Promising Disease for Gene Therapy Development

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1865-8652

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Leber’s Hereditary Optic Neuropathy as a Promising Disease for Gene Therapy Development ; volume:36 ; number:12 ; day:11 ; month:10 ; year:2019 ; pages:3299-3307 ; date:12.2019
Advances in therapy ; 36, Heft 12 (11.10.2019), 3299-3307, 12.2019

Creator: Karaarslan, Cuneyt

Contributor: SpringerLink (Online service)

DOI: 10.1007/s12325-019-01113-2

URN: urn:nbn:de:101:1-2020030900250812097268

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:51 AM CEST

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Karaarslan, Cuneyt
SpringerLink (Online service)

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Leber’s Hereditary Optic Neuropathy as a Promising Disease for Gene Therapy Development

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Other Objects (12)

A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy

Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy

Leber’s hereditary optic neuropathy following unilateral painful optic neuritis: a case report

Developments in the Treatment of Leber Hereditary Optic Neuropathy

Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy

Macular thickness changes in a patient with Leber’s hereditary optic neuropathy

Leber’s hereditary optic neuropathy – current status of idebenone and gene replacement therapies

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Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy

Leber’s hereditary optic neuropathy following unilateral painful optic neuritis: a case report

Developments in the Treatment of Leber Hereditary Optic Neuropathy

Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy

Macular thickness changes in a patient with Leber’s hereditary optic neuropathy

Leber’s hereditary optic neuropathy – current status of idebenone and gene replacement therapies

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Cyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy

Magnetic resonance imaging negative myelopathy in Leber’s hereditary optic neuropathy: a case report

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Characterization of macular thickness changes in Leber’s hereditary optic neuropathy by optical coherence tomography

A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy

Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy

Leber’s hereditary optic neuropathy following unilateral painful optic neuritis: a case report

Developments in the Treatment of Leber Hereditary Optic Neuropathy

Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy

Macular thickness changes in a patient with Leber’s hereditary optic neuropathy

Leber’s hereditary optic neuropathy – current status of idebenone and gene replacement therapies

Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy

Cyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy

Magnetic resonance imaging negative myelopathy in Leber’s hereditary optic neuropathy: a case report

Testosterone increases apoptotic cell death and decreases mitophagy in Leber’s hereditary optic neuropathy cells

Characterization of macular thickness changes in Leber’s hereditary optic neuropathy by optical coherence tomography

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