(Q36846748)

16 August 2017

1 reference

title

Inherited lipodystrophies and the metabolic syndrome (English)

1 reference

16 August 2017

1 reference

3

Robert A Hegele

0 references

author name string

Houshang Monajemi

series ordinal

1

1 reference

PubMed ID

17561981

16 August 2017

Erik Stroes

series ordinal

2

1 reference

PubMed ID

17561981

16 August 2017

Eric Fliers

series ordinal

4

1 reference

16 August 2017

11 June 2007

1 reference

16 August 2017

Clinical Endocrinology

1 reference

16 August 2017

67

1 reference

16 August 2017

4

1 reference

16 August 2017

479-484

1 reference

Acquired and inherited lipodystrophies

16 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

A gene for congenital generalized lipodystrophy maps to human chromosome 9q34.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Body fat distribution and metabolic derangements in patients with familial partial lipodystrophy associated with mandibuloacral dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Human laminopathies: nuclei gone genetically awry

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Hutchinson-Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Progeria: A cell culture study and clinical report of familial incidence

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Lipodystrophy of the extremities. A dominantly inherited syndrome associated with lipatrophic diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Köbberling type of familial partial lipodystrophy: an underrecognized syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

A novel heterozygous mutation in peroxisome proliferator-activated receptor-gamma gene in a patient with familial partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

PPARG F388L, a transactivation-deficient mutant, in familial partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferator-activated receptor-gamma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Semi-automated segmentation and quantification of adipose tissue in calf and thigh by MRI: a preliminary study in patients with monogenic metabolic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

A family with severe insulin resistance and diabetes due to a mutation in AKT2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Leptin-replacement therapy for lipodystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.02906.X

Dominant negative mutations in human PPARgamma associated with severe insulin resistance, diabetes mellitus and hypertension

21 January 2018

1 reference

COCI

https://opencitations.net/index/coci/api/v1/citations/10.1038/47254

10.1111/J.1365-2265.2007.02906.X

15 July 2023

Identifiers

DOI

1 reference

16 August 2017

1 reference

PubMed ID

17561981