| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNA
|
Catarino, Claudia B.
|
|
2017
|
36 |
C |
p. 15-20
6 p.
|
article
|
| 2 |
Disturbed mitochondrial function restricts glutamate uptake in the human Müller glia cell line, MIO-M1
|
Vohra, Rupali
|
|
2017
|
36 |
C |
p. 52-59
8 p.
|
article
|
| 3 |
Editorial Board
|
|
|
2017
|
36 |
C |
p. IFC-
1 p.
|
article
|
| 4 |
Establishment of human retinal mitoscriptome gene expression signature for diabetic retinopathy using cadaver eyes
|
Govindarajan, Gowthaman
|
|
2017
|
36 |
C |
p. 150-181
32 p.
|
article
|
| 5 |
Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy
|
Yu-Wai-Man, Patrick
|
|
2017
|
36 |
C |
p. 36-42
7 p.
|
article
|
| 6 |
Incomplete penetrance in mitochondrial optic neuropathies
|
Caporali, Leonardo
|
|
2017
|
36 |
C |
p. 130-137
8 p.
|
article
|
| 7 |
Melanopsin-expressing retinal ganglion cells are resistant to cell injury, but not always
|
Georg, Birgitte
|
|
2017
|
36 |
C |
p. 77-84
8 p.
|
article
|
| 8 |
Mitochondria and the eye diseases - Editorial
|
Kolko, M.
|
|
2017
|
36 |
C |
p. 1-3
3 p.
|
article
|
| 9 |
Mitochondrial dynamics, transport, and quality control: A bottleneck for retinal ganglion cell viability in optic neuropathies
|
Ito, Yoko A.
|
|
2017
|
36 |
C |
p. 186-192
7 p.
|
article
|
| 10 |
Mitochondrial dysfunction and diabetic retinopathy
|
Bek, Toke
|
|
2017
|
36 |
C |
p. 4-6
3 p.
|
article
|
| 11 |
Mitochondrial dysfunction and oxidative stress in corneal disease
|
Vallabh, Neeru A.
|
|
2017
|
36 |
C |
p. 103-113
11 p.
|
article
|
| 12 |
Mitochondrial dysfunction underlying outer retinal diseases
|
Lefevere, Evy
|
|
2017
|
36 |
C |
p. 66-76
11 p.
|
article
|
| 13 |
Mitochondrial function in Müller cells - Does it matter?
|
Toft-Kehler, Anne Katrine
|
|
2017
|
36 |
C |
p. 43-51
9 p.
|
article
|
| 14 |
No evidence of association between optic neuritis and secondary LHON mtDNA mutations in patients with multiple sclerosis
|
Andalib, Sasan
|
|
2017
|
36 |
C |
p. 182-185
4 p.
|
article
|
| 15 |
Optical coherence tomography angiography of the peripapillary retina and optic nerve head in dominant optic atrophy
|
Balducci, Nicole
|
|
2017
|
36 |
C |
p. 60-65
6 p.
|
article
|
| 16 |
Photostimulation of mitochondria as a treatment for retinal neurodegeneration
|
Beirne, Kathy
|
|
2017
|
36 |
C |
p. 85-95
11 p.
|
article
|
| 17 |
Pupillometric evaluation of the melanopsin containing retinal ganglion cells in mitochondrial and non-mitochondrial optic neuropathies
|
Ba-Ali, Shakoor
|
|
2017
|
36 |
C |
p. 124-129
6 p.
|
article
|
| 18 |
Systemic PTEN-Akt1-mTOR pathway activity in patients with normal tension glaucoma and ocular hypertension: A case series
|
Lascaratos, Gerassimos
|
|
2017
|
36 |
C |
p. 96-102
7 p.
|
article
|
| 19 |
Targeting mitochondrial function to treat optic neuropathy
|
Gueven, Nuri
|
|
2017
|
36 |
C |
p. 7-14
8 p.
|
article
|
| 20 |
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy
|
Majander, A.
|
|
2017
|
36 |
C |
p. 138-149
12 p.
|
article
|
| 21 |
Topical Coenzyme Q10 demonstrates mitochondrial-mediated neuroprotection in a rodent model of ocular hypertension
|
Davis, Benjamin Michael
|
|
2017
|
36 |
C |
p. 114-123
10 p.
|
article
|
| 22 |
Visual light effects on mitochondria: The potential implications in relation to glaucoma
|
Osborne, Neville N.
|
|
2017
|
36 |
C |
p. 29-35
7 p.
|
article
|
| 23 |
Whole mitochondrial genome analysis in South Indian patients with Leber's hereditary optic neuropathy
|
Saikia, Bibhuti Ballav
|
|
2017
|
36 |
C |
p. 21-28
8 p.
|
article
|
Journal description