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Found 11 publications

New possibilities in diagnosis of hereditary optic neuropathies.

Genetic Spectrum and Characteristics of Hereditary Optic Neuropathy in Taiwan.

MCAT Mutations Cause Nuclear LHON-like Optic Neuropathy.

Clinical characteristics and research progress on the treatment of mitochondrial optic neuropathy.

Mitophagy: An Emerging Target in Ocular Pathology.

A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in MT-ND4 Gene (m.11253T>C) and Literature Review.

Sulthiame impairs mitochondrial function in vitro and may trigger onset of visual loss in Leber hereditary optic neuropathy.

Therapeutic Strategies for Attenuation of Retinal Ganglion Cell Injury in Optic Neuropathies: Concepts in Translational Research and Therapeutic Implications.

Multilocus Mitochondrial Mutations Do Not Directly Affect the Efficacy of Gene Therapy for Leber Hereditary Optic Neuropathy.

Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene: A Secondary Analysis of a Phase 1/2 Clinical Trial.

Visual Field Variability after Gene Therapy for Leber's Hereditary Optic Neuropathy.

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