(Q48023965)

7 February 2018

title

Post-mortem findings in familial partial lipodystrophy, Dunnigan variety. (English)

1 reference

7 February 2018

familial partial lipodystrophy

main subject

1 reference

Haque WA

1

1 reference

7 February 2018

Vuitch F

series ordinal

2

1 reference

7 February 2018

Garg A

series ordinal

3

1 reference

7 February 2018

publication date

1 December 2002

1 reference

7 February 2018

published in

Diabetic Medicine

1 reference

7 February 2018

volume

19

1 reference

7 February 2018

issue

12

1 reference

7 February 2018

page(s)

1022-1025

1 reference

7 February 2018

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

1 reference

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/10.1046%2FJ.1464-5491.2002.00796.X

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

Premature atherosclerosis associated with monogenic insulin resistance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

Islet amyloid and type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

Metformin reverses fatty liver disease in obese, leptin-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

A controlled trial of gemfibrozil in the treatment of patients with nonalcoholic steatohepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00796.X

10.1046/J.1464-5491.2002.00796.X

21 January 2018

Identifiers

DOI

1 reference

7 February 2018

PubMed ID

12647844

1 reference

7 February 2018