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Page 1
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. Guénantin AC, et al. Among authors: caron debarle m. Semin Cell Dev Biol. 2014 May;29:148-57. doi: 10.1016/j.semcdb.2013.12.015. Epub 2013 Dec 30. Semin Cell Dev Biol. 2014. PMID: 24384368 Review.
Human lipodystrophies: genetic and acquired diseases of adipose tissue.
Capeau J, Magré J, Caron-Debarle M, Lagathu C, Antoine B, Béréziat VR, Lascols O, Bastard JP, Vigouroux C. Capeau J, et al. Among authors: caron debarle m. Endocr Dev. 2010;19:1-20. doi: 10.1159/000316893. Epub 2010 Jun 15. Endocr Dev. 2010. PMID: 20551664 Free PMC article. Review.
PIK3R1 mutations cause syndromic insulin resistance with lipoatrophy.
Thauvin-Robinet C, Auclair M, Duplomb L, Caron-Debarle M, Avila M, St-Onge J, Le Merrer M, Le Luyer B, Héron D, Mathieu-Dramard M, Bitoun P, Petit JM, Odent S, Amiel J, Picot D, Carmignac V, Thevenon J, Callier P, Laville M, Reznik Y, Fagour C, Nunes ML, Capeau J, Lascols O, Huet F, Faivre L, Vigouroux C, Rivière JB. Thauvin-Robinet C, et al. Among authors: caron debarle m. Am J Hum Genet. 2013 Jul 11;93(1):141-9. doi: 10.1016/j.ajhg.2013.05.019. Epub 2013 Jun 27. Am J Hum Genet. 2013. PMID: 23810378 Free PMC article.
Peroxisome proliferator-activated receptor-γ mutations responsible for lipodystrophy with severe hypertension activate the cellular renin-angiotensin system.
Auclair M, Vigouroux C, Boccara F, Capel E, Vigeral C, Guerci B, Lascols O, Capeau J, Caron-Debarle M. Auclair M, et al. Among authors: caron debarle m. Arterioscler Thromb Vasc Biol. 2013 Apr;33(4):829-38. doi: 10.1161/ATVBAHA.112.300962. Epub 2013 Feb 7. Arterioscler Thromb Vasc Biol. 2013. PMID: 23393388
20 results