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Subclinical multisystem neurologic disease in "pure" OPA1 autosomal dominant optic atrophy
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
title
Subclinical multisystem neurologic disease in "pure" OPA1 autosomal dominant optic atrophy
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
main subject
autosomal dominant optic atrophy
0 references
author
Mark R Baker
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
Roger Whittaker
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
Patrick Yu-Wai-Man
series ordinal
5
object named as
P Yu-Wai-Man
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
author name string
K M Fisher
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
P G Griffiths
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
P F Chinnery
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
language of work or name
English
0 references
publication date
14 September 2011
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
published in
Neurology
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
volume
77
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
issue
13
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
page(s)
1309-1312
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
cites work
Heterozygous OPA1 mutations in Behr syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179647
retrieved
13 July 2018
Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179647
retrieved
13 July 2018
Multi-system neurological disease is common in patients with OPA1 mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179647
retrieved
13 July 2018
Mitochondrial defects in acute multiple sclerosis lesions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179647
retrieved
13 July 2018
OPA1 mutations and mitochondrial DNA damage: keeping the magic circle in shape
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179647
retrieved
13 July 2018
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179647
retrieved
26 September 2018
Central motor conduction differs between acute relapsing–remitting and chronic progressive multiple sclerosis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21917770
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1212/WNL.0B013E318230A15A
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
PMC publication ID
3179647
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
PubMed publication ID
21917770
1 reference
stated in
Europe PubMed Central
PMC publication ID
3179647
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21917770%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 February 2020
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