Developments in the Treatment of Leber Hereditary Optic Neuropathy

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1534-6293

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Developments in the Treatment of Leber Hereditary Optic Neuropathy ; volume:22 ; number:12 ; day:21 ; month:11 ; year:2022 ; pages:881-892 ; date:12.2022
Current neurology and neuroscience reports ; 22, Heft 12 (21.11.2022), 881-892, 12.2022

Creator: Chen, Benson S.
Yu-Wai-Man, Patrick
Newman, Nancy J.

Contributor: SpringerLink (Online service)

DOI: 10.1007/s11910-022-01246-y

URN: urn:nbn:de:101:1-2023022321152440010758

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

Last update: 14.08.2025, 10:46 AM CEST

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Chen, Benson S.
Yu-Wai-Man, Patrick
Newman, Nancy J.
SpringerLink (Online service)

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Developments in the Treatment of Leber Hereditary Optic Neuropathy

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Other Objects (12)

Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy

A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy

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

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

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

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

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

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

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Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study

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

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A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy

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

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

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

Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy

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

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

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

Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study

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

Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy

A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy

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

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

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

Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy

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

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

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

Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study

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