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English
Wolfram (DIDMOAD) syndrome.
scientific article published on October 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Wolfram (DIDMOAD) syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
author
Timothy Barrett
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
author name string
S E Bundey
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
language of work or name
English
0 references
publication date
1 October 1997
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
34
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
10
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
838-841
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
cites work
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.
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=1051091
retrieved
6 October 2017
Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion
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=1051091
retrieved
6 October 2017
Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4
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=1051091
retrieved
6 October 2017
Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) 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=1051091
retrieved
6 October 2017
DIDMOAD syndrome with megacystis and megaureter
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=1051091
retrieved
6 October 2017
Wolfram's syndrome: a clinical, diagnostic, and interpretative contribution
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=1051091
retrieved
6 October 2017
Psychiatric findings in Wolfram syndrome homozygotes
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=1051091
retrieved
6 October 2017
Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive 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=1051091
retrieved
6 October 2017
Wolfram syndrome: Evidence of a diffuse neurodegenerative disease by magnetic resonance imaging
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=1051091
retrieved
6 June 2018
Juvenile diabetes mellitus, optic atrophy, sensory nerve deafness, and diabetes insipidus--a 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=1051091
retrieved
6 June 2018
Recessive inheritance of diabetes: the syndrome of diabetes insipidus, diabetes mellitus, optic atrophy and deafness.
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=1051091
retrieved
6 June 2018
Simultaneous occurrence of diabetes mellitus, diabetes insipidus, and optic atrophy in a brother and sister
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=1051091
retrieved
6 June 2018
The relation of spinal cord diseases to gynecomastia and testicular atrophy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9350817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Primary optic atrophy in diabetes mellitus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9350817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Successful pregnancy in two sisters with Wolfram syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9350817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Optic atrophy in Wolfram syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9350817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
DIDMOAD syndrome; further studies and muscle biochemistry
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9350817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Vasopressin secretion in the DIDMOAD (Wolfram) syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9350817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mitochondrial abnormalities in the DIDMOAD syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9350817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Wolfram syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9350817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.34.10.838
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
PMCID
1051091
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
PubMed ID
9350817
1 reference
stated in
Europe PubMed Central
PMCID
1051091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9350817%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
ResearchGate publication ID
13878185
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