Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q74095938)
Watch
English
Optic neuropathy in Lhon and Leigh syndrome
scientific article published on 01 July 2001
In more languages
default values for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
title
Optic neuropathy in Lhon and Leigh syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author name string
V Carelli
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
A A Sadun
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
publication date
1 July 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Ophthalmology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
108
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
1172-1173
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
Ocular histopathologic study of a patient with the T 8993-G point mutation in Leigh's syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900618-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations and pathogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900618-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathogenic factors underlying the lesions in Leigh's disease. Tissue responses to cellular energy deprivation and their clinico-pathological consequences
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900618-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900618-2
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900618-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900618-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900618-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0161-6420(01)00618-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed publication ID
11425664
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11425664
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425664%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit