Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber’s Hereditary Optic Neuropathy during One Year of Follow-up-Reference-Cited by-同舟云学术

Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber’s Hereditary Optic Neuropathy during One Year of Follow-up

Published:2019-07 Issue:7 Volume:126 Page:1033-1044
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Parisi Vincenzo,Ziccardi Lucia^ORCID,Sadun Federico,De Negri Anna Maria,La Morgia Chiara,Barbano Lucilla,Carelli Valerio,Barboni Piero

Funder

Fondazione Roma

Ministero della Salute

Publisher

Elsevier BV

Subject

Ophthalmology

Reference49 articles.

1. Mitochondrial ophthalmology;Carelli,2006

2. Mitochondrial dysfunction as a cause of optic neuropathies;Carelli;Prog Retin Eye Res,2004

3. Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber’s hereditary optic neuropathy;Fauser;Ophthalmic Genet,2002

4. Low-penetrance branches in matrilineal pedigrees with Leber hereditary optic neuropathy;Howell;Am J Hum Genet,1998

5. Leber’s hereditary optic neuropathy;Carelli,2002

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3. PhNR and peripapillary RNFL changes in Leber hereditary optic neuropathy with m.G11778A mutation;Mitochondrion;2023-05

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