Leber hereditary optic neuropathy: respiratory chain dysfunction and degeneration of the optic nerve (Q74783603)

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scientific article published on 01 May 1998

Language	Label	Description	Also known as
English	Leber hereditary optic neuropathy: respiratory chain dysfunction and degeneration of the optic nerve	scientific article published on 01 May 1998

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference

Europe PubMed Central

Leber hereditary optic neuropathy: respiratory chain dysfunction and degeneration of the optic nerve (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

Leber hereditary optic neuropathy

1 reference

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author name string

N Howell

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

publication date

1 May 1998

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

Vision Research

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

38

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1495-1504

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

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

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Race-, age-, gender-, and refractive error-related differences in the normal optic disc

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Number of people with glaucoma worldwide

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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mtDNA Mutations That Cause Optic Neuropathy: How Do We Know?

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mastocytosis-induced nyctalopia

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for preserved direct pupillary light response in Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A case-control study of Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of the 11778 mitochondrial DNA mutation and demyelinating disease

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Leber's hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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Tobacco amblyopia

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Leber's hereditary optic neuropathy and complex I deficiency in muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Platelet mitochondrial function in Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype.

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chain

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Adenosine triphosphate deficiency: a genre of optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Energy metabolism of rabbit retina as related to function: high cost of Na+ transport

1 reference

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7 January 2021

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Chloramphenicol for long-term therapy of cystic fibrosis

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based on heuristic

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Optic neuritis with prolonged use of chloramphenicol. Case report and relationship to fundus changes in cystic fibrosis

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Visual disturbances in cystic fibrosis following chloramphenicol administration

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Optic disk risk factors for nonarteritic anterior ischemic optic neuropathy.

1 reference

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7 January 2021

based on heuristic

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Mechanisms of optic nerve damage in primary open angle glaucoma

1 reference

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7 January 2021

based on heuristic

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The histochemical localization of cytochrome oxidase in the retina and lateral geniculate nucleus of the ferret, cat, and monkey, with particular reference to retinal mosaics and ON/OFF-center visual channels

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence of constriction of optic nerve axons at the lamina cribrosa in the normotensive eye in humans and other mammals

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

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Mitochondrial permeability transition is a central coordinating event of apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial dysfunction is a primary event in glutamate neurotoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Why are mitochondria involved in apoptosis? Permeability transition pores and apoptosis as selective mechanisms to eliminate superoxide-producing mitochondria and cell.

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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Mitochondrial production of reactive oxygen species in cortical neurons following exposure to N-methyl-D-aspartate

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

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Complex I inhibitors induce dose-dependent apoptosis in PC12 cells: relevance to Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

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Mitochondrial respiratory chain inhibitors induce apoptosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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Apoptotic cell death induced by optic nerve lesion in the neonatal rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

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Long-term survival of retinal ganglion cells following optic nerve section in adult bcl-2 transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

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The nerve of glaucoma!

1 reference

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7 January 2021

based on heuristic

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1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2897%2900444-6

7 January 2021

based on heuristic

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Identifiers

10.1016/S0042-6989(97)00444-6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9667014%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

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