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Items: 1 to 20 of 329

1.

Diseases of adipose tissue: genetic and acquired lipodystrophies.

Capeau J, Magré J, Lascols O, Caron M, Béréziat V, Vigouroux C, Bastard JP.

Biochem Soc Trans. 2005 Nov;33(Pt 5):1073-7. Review.

PMID:
16246048
2.

[Lipodystrophic syndromes: congenital or acquired diseases of adipose tissue].

Capeau J, Vigouroux C, Magré J, Lascols O, Caron M, Bastard JP.

C R Biol. 2006 Aug;329(8):639-52; discussion 653-5. Epub 2006 Apr 27. French.

PMID:
16860281
3.

[Primary lipodystrophies].

Capeau J, Magré J, Lascols O, Caron M, Béréziat V, Vigouroux C.

Ann Endocrinol (Paris). 2007 Feb;68(1):10-20. Epub 2007 Feb 21. French.

PMID:
17320032
4.

Lipodystrophies.

Garg A.

Am J Med. 2000 Feb;108(2):143-52. Review.

PMID:
11126308
5.

Human lipodystrophies: genetic and acquired diseases of adipose tissue.

Capeau J, Magré J, Caron-Debarle M, Lagathu C, Antoine B, Béréziat V, Lascols O, Bastard JP, Vigouroux C.

Endocr Dev. 2010;19:1-20. doi: 10.1159/000316893. Epub 2010 Jun 15. Review.

6.

Monogenic forms of insulin resistance: apertures that expose the common metabolic syndrome.

Hegele RA.

Trends Endocrinol Metab. 2003 Oct;14(8):371-7. Review.

PMID:
14516935
7.

A-type lamin-linked lipodystrophies.

Vigouroux C, Capeau J.

Novartis Found Symp. 2005;264:166-77; discussion 177-82, 227-30. Review.

PMID:
15773753
8.

Thematic review series: Adipocyte Biology. Lipodystrophies: windows on adipose biology and metabolism.

Hegele RA, Joy TR, Al-Attar SA, Rutt BK.

J Lipid Res. 2007 Jul;48(7):1433-44. Epub 2007 Mar 20. Review.

9.

Molecular mechanisms of human lipodystrophies: from adipocyte lipid droplet to oxidative stress and lipotoxicity.

Vigouroux C, Caron-Debarle M, Le Dour C, Magré J, Capeau J.

Int J Biochem Cell Biol. 2011 Jun;43(6):862-76. doi: 10.1016/j.biocel.2011.03.002. Epub 2011 Mar 8. Review.

PMID:
21392585
10.

Lessons from human mutations in PPARgamma.

Hegele RA.

Int J Obes (Lond). 2005 Mar;29 Suppl 1:S31-5.

PMID:
15711581
11.

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

Bidault G, Vatier C, Capeau J, Vigouroux C, Béréziat V.

Biochem Soc Trans. 2011 Dec;39(6):1752-7. doi: 10.1042/BST20110675. Review.

PMID:
22103520
12.

The molecular basis of genetic lipodystrophies.

Bhayana S, Hegele RA.

Clin Biochem. 2002 May;35(3):171-7. Review.

PMID:
12074822
13.

Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation.

Mory PB, Crispim F, Kasamatsu T, Gabbay MA, Dib SA, Moisés RS.

Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1252-6.

14.

Central players in inherited lipodystrophies.

Jeninga EH, Kalkhoven E.

Trends Endocrinol Metab. 2010 Oct;21(10):581-8. doi: 10.1016/j.tem.2010.06.006. Epub 2010 Jul 10.

PMID:
20621503
15.

Prevalence of mutations in AGPAT2 among human lipodystrophies.

Magré J, Delépine M, Van Maldergem L, Robert JJ, Maassen JA, Meier M, Panz VR, Kim CA, Tubiana-Rufi N, Czernichow P, Seemanova E, Buchanan CR, Lacombe D, Vigouroux C, Lascols O, Kahn CR, Capeau J, Lathrop M.

Diabetes. 2003 Jun;52(6):1573-8.

16.

Lipoatrophy revisited.

Reitman ML, Arioglu E, Gavrilova O, Taylor SI.

Trends Endocrinol Metab. 2000 Dec;11(10):410-6. Review.

PMID:
11091118
17.

[Lipodystrophies].

Fardet L, Vigouroux C, Capeau J.

Rev Med Interne. 2013 Oct;34(10):614-22. doi: 10.1016/j.revmed.2012.11.008. Epub 2012 Dec 31. Review. French.

PMID:
23287278
18.

Genetic forms of the cardiometabolic syndrome: what can they tell the clinician?

Yuan G, Hegele RA.

J Cardiometab Syndr. 2007 Winter;2(1):45-8. Review.

19.

Nuclear envelope-related lipodystrophies.

Guénantin AC, Briand N, Bidault G, Afonso P, Béréziat V, Vatier C, Lascols O, Caron-Debarle M, Capeau J, Vigouroux C.

Semin Cell Dev Biol. 2014 May;29:148-57. doi: 10.1016/j.semcdb.2013.12.015. Epub 2013 Dec 30. Review.

PMID:
24384368
20.

Molecular basis of partial lipodystrophy and prospects for therapy.

Hegele RA.

Trends Mol Med. 2001 Mar;7(3):121-6. Review.

PMID:
11286783

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