Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.

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

Optic neuropathies.

Gene therapy, CMT1X, and the inherited neuropathies.

Ischemic Optic Neuropathies.

Inflammatory optic neuropathies.

Congenital optic nerve anomalies and hereditary optic neuropathies.

Effect of pain in pediatric inherited neuropathies.

Metabolic, hereditary, traumatic, and neoplastic optic neuropathies.

Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness Measurements.

Charcot-Marie-Tooth disease and other inherited neuropathies.

Diffusion Tensor Imaging Mapping of Brain White Matter Pathology in Mitochondrial Optic Neuropathies.

Medical management of hereditary optic neuropathies.

Infectious optic neuropathies: a clinical update.

Improving diagnosis of inherited peripheral neuropathies through gene panel analysis.

Autophagy as an Emerging Common Pathomechanism in Inherited Peripheral Neuropathies.

The morphological difference between glaucoma and other optic neuropathies.

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies.

Altered mitochondrial membrane activities associated with cytoplasmically-inherited disease sensitivity in maize.

Molecular regulators of nerve conduction - Lessons from inherited neuropathies and rodent genetic models.

Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges.

ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia.

Mitochondrial DNA deletions in inherited recurrent myoglobinuria.

Blocking mitochondrial calcium release in Schwann cells prevents demyelinating neuropathies.

Mitochondrial mutations in maternally inherited hearing loss.

Suggest Documents

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

Optic neuropathies.

Gene therapy, CMT1X, and the inherited neuropathies.

Ischemic Optic Neuropathies.

Inflammatory optic neuropathies.

Congenital optic nerve anomalies and hereditary optic neuropathies.

Effect of pain in pediatric inherited neuropathies.

Metabolic, hereditary, traumatic, and neoplastic optic neuropathies.

Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness Measurements.

Charcot-Marie-Tooth disease and other inherited neuropathies.

Diffusion Tensor Imaging Mapping of Brain White Matter Pathology in Mitochondrial Optic Neuropathies.

Medical management of hereditary optic neuropathies.

Infectious optic neuropathies: a clinical update.

Improving diagnosis of inherited peripheral neuropathies through gene panel analysis.

Autophagy as an Emerging Common Pathomechanism in Inherited Peripheral Neuropathies.

The morphological difference between glaucoma and other optic neuropathies.

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies.

Altered mitochondrial membrane activities associated with cytoplasmically-inherited disease sensitivity in maize.

Molecular regulators of nerve conduction - Lessons from inherited neuropathies and rodent genetic models.

Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges.

ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia.

Mitochondrial DNA deletions in inherited recurrent myoglobinuria.

Blocking mitochondrial calcium release in Schwann cells prevents demyelinating neuropathies.

Mitochondrial mutations in maternally inherited hearing loss.

Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.

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