Treatment strategies for inherited optic neuropathies: past, present and future (Q33595163)

28 July 2017

1 reference

25 April 2019

Treatment strategies for inherited optic neuropathies: past, present and future (English)

1 reference

autosomal dominant optic atrophy

28 July 2017

1 reference

Leber hereditary optic neuropathy

25 April 2019

1 reference

25 April 2019

M Votruba

2

0 references

Patrick F. Chinnery

series ordinal

4

object named as

P F Chinnery

1 reference

28 July 2017

1

P Yu-Wai-Man

1 reference

28 July 2017

3

A T Moore

1 reference

28 July 2017

language of work or name

1 reference

7 March 2014

1 reference

28 July 2017

1 May 2014

4 references

5 March 2019

24 March 2019

22 April 2019

25 April 2019

5 references

28 July 2017

5 March 2019

24 March 2019

22 April 2019

25 April 2019

28

1 reference

28 July 2017

5

1 reference

28 July 2017

521-537

1 reference

Creative Commons Attribution 3.0 Unported

28 July 2017

4 references

5 March 2019

24 March 2019

22 April 2019

on focus list of Wikimedia project

25 April 2019

copyright status

copyrighted

0 references

ScienceSource

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/eye.2014.37

0 references

cites work

Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Next-generation sequencing of mitochondrial targeted AAV transfer of human ND4 in mice

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic Neuropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Loss of OPA1 disturbs cellular calcium homeostasis and sensitizes for excitotoxicity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mouse mtDNA mutant model of Leber hereditary optic neuropathy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Towards germline gene therapy of inherited mitochondrial diseases

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Treatment of hereditary optic neuropathies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber's hereditary optic neuropathy in a mouse model.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Treatment for mitochondrial disorders

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Effect of EPI-743 on the clinical course of the mitochondrial disease Leber hereditary optic neuropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Disorders of the optic nerve in mitochondrial cytopathies: new ideas on pathogenesis and therapeutic targets

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial gene therapy improves respiration, biogenesis, and transcription in G11778A Leber's hereditary optic neuropathy and T8993G Leigh's syndrome cells.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Autologous mesenchymal stem cells for the treatment of secondary progressive multiple sclerosis: an open-label phase 2a proof-of-concept study

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial DNA disease: new options for prevention

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Stemming vision loss with stem cells

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

A neurological perspective on mitochondrial disease.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

The neuro-ophthalmology of mitochondrial disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

The prevalence and natural history of dominant optic atrophy due to OPA1 mutations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Neuroprotective effects of intravitreal mesenchymal stem cell transplantation in experimental glaucoma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Multiple sclerosis associated with Leber's Hereditary Optic Neuropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Efficiency and safety of AAV-mediated gene delivery of the human ND4 complex I subunit in the mouse visual system

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Quality of life in patients with leber hereditary optic neuropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mammalian mitochondrial nucleoids: organizing an independently minded genome.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Axonal loss and neuroprotection in optic neuropathies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Use of mitochondrial antioxidant defenses for rescue of cells with a Leber hereditary optic neuropathy-causing mutation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial DNA polymerase-gamma and human disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Clinical and Experimental Applications of NIR-LED Photobiomodulation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Prophylaxis for second eye involvement in leber hereditary optic neuropathy: an open-labeled, nonrandomized multicenter trial of topical brimonidine purite

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial dysfunction as a cause of optic neuropathies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial respiratory-chain diseases

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

The epidemiology of Leber hereditary optic neuropathy in the North East of England

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Leber's hereditary optic neuropathy differentially affects smaller axons in the optic nerve.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

New therapies for optic neuropathies: development in experimental models

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Do idebenone and vitamin therapy shorten the time to achieve visual recovery in Leber hereditary optic neuropathy?

28 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

28 July 2018

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Remission of Leber's hereditary optic neuropathy with idebenone

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.

28 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Inherited mitochondrial optic neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Association of optic disc size with development and prognosis of Leber's hereditary optic neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Gene-environment interactions in Leber hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Multi-system neurological disease is common in patients with OPA1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Hereditary optic neuropathies share a common mitochondrial coupling defect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Visual and psychological morbidity among patients with autosomal dominant optic atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

New treatments for mitochondrial disease-no time to drop our standards

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Idebenone treatment in Leber's hereditary optic neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Current prospects in optic nerve protection and regeneration: sixth ARVO/Pfizer Ophthalmics Research Institute conference.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

mtDNA mutations confer cellular sensitivity to oxidant stress that is partially rescued by calcium depletion and cyclosporin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Idebenone treatment in patients with OPA1-mutant dominant optic atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Acetyl-L-carnitine supplementation to old rats partially reverts the age-related mitochondrial decay of soleus muscle by activating peroxisome proliferator-activated receptor gamma coactivator-1alpha-dependent mitochondrial biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Acetyl-L-carnitine activates the peroxisome proliferator-activated receptor-γ coactivators PGC-1α/PGC-1β-dependent signaling cascade of mitochondrial biogenesis and decreases the oxidized peroxiredoxins content in old rat liver.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

In vivo complementation of complex I by the yeast Ndi1 enzyme. Possible application for treatment of Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Current approaches and future prospects for stem cell rescue and regeneration of the retina and optic nerve.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Mitochondrial gene replacement in primate offspring and embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Subclinical carriers and conversions in Leber hereditary optic neuropathy: a prospective psychophysical study

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Leber's hereditary optic neuropathy with childhood onset

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017118

Evidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy

30 October 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2014.37

Hyperbaric oxygen therapy in the treatment of radiation optic neuropathy

21 January 2018

1 reference

12 December 2020

Rapid visual recovery after coenzyme q10 treatment of leber hereditary optic neuropathy

1 reference

12 December 2020

Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation

1 reference

12 December 2020

Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations

1 reference

12 December 2020

Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function

1 reference

12 December 2020

[Response to idebenone and multivitamin therapy in Leber's hereditary optic neuropathy]

1 reference

12 December 2020

Mitochondrial diseases

1 reference

12 December 2020

Identifiers

DOI

10.1038/EYE.2014.37

1 reference

Dimensions Publication ID

28 July 2017

0 references

1 reference

28 July 2017

1 reference