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English
Cardiomyopathy in congenital complete lipodystrophy
scientific article published on 01 April 2002
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
title
Cardiomyopathy in congenital complete lipodystrophy
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
main subject
cardiomyopathy
1 reference
based on heuristic
inferred from title
author name string
S Bhayana
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
V M Siu
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
G I Joubert
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
C L Clarson
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
H Cao
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
R A Hegele
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
publication date
1 April 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
volume
61
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
page(s)
283-287
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
cites work
Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The envelope, please: nuclear lamins and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Premature atherosclerosis associated with monogenic insulin resistance.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GENERALIZED LIPODYSTROPHY.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A Gene for Congenital Generalized Lipodystrophy Maps to Human Chromosome 9q34
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Echocardiographic assessment of cardiac function and morphology in patients with generalised lipodystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac findings in generalized lipodystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypertrophic cardiomyopathy in total lipodystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac involvement in total generalized lipodystrophy (Berardinelli- Seip syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac septal hypertrophy in hyperinsulinemic infants
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disproportionate ventricular septal thickening in the developing normal human heart
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dual regulation of glycogen metabolism by insulin and insulin-like growth factors in human hepatoma cells (HEP-G2). Analysis with an anti-receptor monoclonal antibody
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leprechaunism: in vitro insulin action despite genetic insulin resistance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypertrophic cardiomyopathy in total lipodystrophy: insulin action in the face of insulin resistance?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long-term follow up in type A insulin resistant syndrome treated by insulin-like growth factor I.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610407.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1034/J.1399-0004.2002.610407.X
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
PubMed ID
12030893
1 reference
stated in
Europe PubMed Central
PubMed ID
12030893
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12030893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
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