(Q34404123)

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Trial end points and natural history in patients with G11778A Leber hereditary optic neuropathy : preparation for gene therapy clinical trial

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Trial end points and natural history in patients with G11778A Leber hereditary optic neuropathy : preparation for gene therapy clinical trial (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

0 references

Leber hereditary optic neuropathy

1 reference

based on heuristic

inferred from title

Giovanni Gregori

7

object named as

Giovanni Gregori

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

author name string

Byron L Lam

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

William J Feuer

2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Joyce C Schiffman

3

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Vittorio Porciatti

4

1 reference

Europe PubMed Central

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2 August 2017

Ruth Vandenbroucke

5

1 reference

Europe PubMed Central

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2 August 2017

Potyra R Rosa

6

1 reference

Europe PubMed Central

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2 August 2017

John Guy

8

1 reference

Europe PubMed Central

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2 August 2017

language of work or name

0 references

publication date

1 April 2014

1 reference

Europe PubMed Central

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2 August 2017

JAMA Ophthalmology

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Europe PubMed Central

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2 August 2017

132

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Europe PubMed Central

PubMed publication ID

2 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

428-436

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Leber hereditary optic neuropathy gene therapy clinical trial recruitment: year 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Induction of rapid and highly efficient expression of the human ND4 complex I subunit in the mouse visual system by self-complementary adeno-associated virus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Agreement between spectral-domain and time-domain OCT for measuring RNFL thickness.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Reproducibility of pattern electroretinogram in glaucoma patients with a range of severity of disease with the new glaucoma paradigm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Genetic testing for inherited eye disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

The relationship between retinal ganglion cell function and retinal nerve fiber thickness in early glaucoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Pattern electroretinogram abnormality and glaucoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Normative data for a user-friendly paradigm for pattern electroretinogram recording

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Macular nerve fibers temporal to fovea may have a greater potential to recover function in patients with Leber's hereditary optic neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Variable pattern of visual recovery of Leber's hereditary optic neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Protein import into mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

6 July 2018

Idebenone treatment in Leber's hereditary optic neuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

27 October 2018

Screening the three LHON primary mutations in the general Chinese population by using an optimized multiplex allele-specific PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

27 October 2018

Comparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber's hereditary optic neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

27 October 2018

Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

27 October 2018

Leber’s Hereditary Optic Neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266137

27 October 2018

Protein import into mitochondria: two systems acting in tandem?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24525545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/24525545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progression of visual field defects in leber hereditary optic neuropathy: experience of the LHON treatment trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/24525545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visual observations of an American patient with Leber hereditary optic neuropathy after purported injections of stem cells in China

1 reference

https://pubmed.ncbi.nlm.nih.gov/24525545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/24525545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1001/JAMAOPHTHALMOL.2013.7971

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

release_wsdr7z4usjeapo3a6aihvp772y

1 reference

https://api.fatcat.wiki/v0/release/wsdr7z4usjeapo3a6aihvp772y

24 November 2022

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mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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