(Q34954748)

5 August 2017

title

Cardiomyopathy in congenital and acquired generalized lipodystrophy: a clinical assessment (English)

1 reference

acquired generalized lipodystrophy

5 August 2017

0 references

1 reference

1 reference

Beatrice C Lupsa

1

1 reference

5 August 2017

Vandana Sachdev

2

1 reference

5 August 2017

Andreea O Lungu

3

1 reference

5 August 2017

Douglas R Rosing

4

1 reference

5 August 2017

Phillip Gorden

5

1 reference

5 August 2017

language of work or name

English

0 references

publication date

1 July 2010

1 reference

5 August 2017

1 reference

5 August 2017

volume

89

1 reference

5 August 2017

issue

4

1 reference

5 August 2017

page(s)

245-250

1 reference

Lipodystrophy and hepatomegaly, with diabetes, lipaemia, and other metabolic disturbances; a case throwing new light on the action of insulin.

5 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Efficacy of leptin therapy in the different forms of human lipodystrophy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Dilated cardiomyopathy and myocardial infarction secondary to congenital generalized lipodystrophy.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Forgotten but not gone: the rediscovery of fatty heart, the most common unrecognized disease in America

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Laminopathies: multisystem dystrophy syndromes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Hyperleptinemia prevents lipotoxic cardiomyopathy in acyl CoA synthase transgenic mice

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Leptin reverses insulin resistance and hepatic steatosis in patients with severe lipodystrophy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Cardiac involvement in total generalized lipodystrophy (Berardinelli- Seip syndrome).

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Generalized lipodystrophy, congenital and acquired (lipoatrophy).

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Hypertrophic cardiomyopathy in total lipodystrophy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Recommendations for chamber quantification: a report from the American Society of Echocardiography's Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardio

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Long-term efficacy of leptin replacement in patients with generalized lipodystrophy

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Lipodystrophy and gigantism with associated endocrine manifestations. A new diencephalic syndrome?

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Cardiomyopathy in lipodystrophy and the specificity spillover hypothesis.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090142

Cardiomyopathy in congenital complete lipodystrophy

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20616664

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Total lipodystrophy with heart failure and renal failure: report of a case

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20616664

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Echocardiographic assessment of cardiac function and morphology in patients with generalised lipodystrophy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20616664

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1097/MD.0B013E3181E9442F

1 reference

5 August 2017

1 reference

5 August 2017

1 reference