(Q34453418)

2 August 2017

title

Hepatic steatosis in Dunnigan-type familial partial lipodystrophy (English)

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familial partial lipodystrophy

2 August 2017

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Angelika Lüdtke

1

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2 August 2017

Janine Genschel

2

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2 August 2017

Georg Brabant

3

1 reference

2 August 2017

Jürgen Bauditz

4

1 reference

2 August 2017

Matthias Taupitz

5

1 reference

2 August 2017

Martin Koch

6

1 reference

2 August 2017

Wolfram Wermke

7

1 reference

2 August 2017

Howard J Worman

8

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2 August 2017

Hartmut H-J Schmidt

9

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2 August 2017

language of work or name

English

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publication date

1 October 2005

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The American Journal of Gastroenterology

2 August 2017

published in

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2 August 2017

volume

100

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2 August 2017

issue

10

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2 August 2017

page(s)

2218-2224

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Definition of metabolic syndrome: report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

Nonalcoholic fatty liver disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.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.1572-0241.2005.00234.X

Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in the LMNA gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.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.1572-0241.2005.00234.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

Mutations in the LMNA gene encoding lamin A/C

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

The inner nuclear membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

Post-mortem findings in familial partial lipodystrophy, Dunnigan variety

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

An International Classification of Hyperlipidemias and Hyperlipoproteinemias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2005.00234.X

10.1111/J.1572-0241.2005.00234.X

21 January 2018

Identifiers

DOI

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2 August 2017

1 reference