Bone imaging findings in genetic and acquired lipodystrophic syndromes: an imaging study of 24 cases-Reference-Cited by-同舟云学术

Bone imaging findings in genetic and acquired lipodystrophic syndromes: an imaging study of 24 cases

Published:2016-09-08 Issue:11 Volume:45 Page:1495-1506
ISSN:0364-2348
Container-title:Skeletal Radiology
language:en
Short-container-title:Skeletal Radiol

Author:

Teboul-Coré Stephanie,Rey-Jouvin Caroline,Miquel Anne,Vatier Camille,Capeau Jacqueline,Robert Jean-Jacques,Pham Thao,Lascols Olivier,Berenbaum Francis,Laredo Jean-Denis,Vigouroux Corinne,Sellam Jérémie

Publisher

Springer Science and Business Media LLC

Subject

Radiology, Nuclear Medicine and imaging

Link

http://link.springer.com/content/pdf/10.1007/s00256-016-2457-9.pdf

Reference30 articles.

1. Robbins AL, Savage DB. The genetics of lipid storage and human lipodystrophies. Trends Mol Med. 2015;21(7):433–8.

2. Agarwal AK, Arioglu E, de Almeida S, et al. AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34. Nat Genet. 2002;31(1):21–3.

3. Magré J, Delépine M, Khallouf E, et al. Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nat Genet. 2001;28(4):365–70.

4. Shackleton S, Lloyd DJ, Jackson SN, et al. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy. Nat Genet. 2000;24(2):153–6.

5. Barroso I, Gurnell M, Crowley VEF, et al. Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension. Nature. 1999;402(6764):880–3.

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