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Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case
scientific article published on 01 October 1995
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1 reference
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Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
title
Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
author name string
J B Kerrison
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
N Howell
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
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2 November 2019
N R Miller
series ordinal
3
1 reference
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Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
L Hirst
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
W R Green
series ordinal
5
1 reference
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Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
publication date
1 October 1995
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
published in
Ophthalmology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
volume
102
1 reference
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Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
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2 November 2019
issue
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
page(s)
1509-1516
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
cites work
Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's hereditary optic atrophy: some clinical and aetiological considerations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Further clinical and pathological observations on Leber's optic atrophy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
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Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findings
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber hereditary optic neuropathy in Australia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
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Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
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The effect of formalin fixation on DNA and the extraction of high-molecular-weight DNA from fixed and embedded tissues
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetic analyses of the Tyrolean Ice Man
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
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7 January 2021
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inferred from DOI database lookup
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1 reference
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7 January 2021
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Tobacco-alcohol amblyopia. Further comments on its pathology
1 reference
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Crossref
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7 January 2021
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Ocular Fundus in Acute Leber Optic Neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The early phase in Leber hereditary optic atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Fundus changes in acute malnutritional optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
retrieved
7 January 2021
based on heuristic
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Leber's hereditary optic neuroretinopathy, a mitochondrial disease?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930838-X
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7 January 2021
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Leber's disease and dystonia: a mitochondrial disease
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Crossref
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7 January 2021
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Studies on the pathogenesis of ischemic cell injury. VI. Mitochondrial flocculent densities in autolysis
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Excitotoxins: possible mechanisms of action
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1 reference
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7 January 2021
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Identifiers
DOI
10.1016/S0161-6420(95)30838-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
PubMed publication ID
9097799
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9097799
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9097799%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
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