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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: magre j. Endocr Dev. 2010;19:1-20. doi: 10.1159/000316893. Epub 2010 Jun 15. Endocr Dev. 2010. PMID: 20551664 Free PMC article. Review.
Diseases of adipose tissue: genetic and acquired lipodystrophies.
Capeau J, Magré J, Lascols O, Caron M, Béréziat V, Vigouroux C, Bastard JP. Capeau J, et al. Among authors: magre j. Biochem Soc Trans. 2005 Nov;33(Pt 5):1073-7. doi: 10.1042/BST0331073. Biochem Soc Trans. 2005. PMID: 16246048 Review.
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. Magré J, et al. Diabetes. 2003 Jun;52(6):1573-8. doi: 10.2337/diabetes.52.6.1573. Diabetes. 2003. PMID: 12765973
Higher adiponectin levels in patients with Berardinelli-Seip congenital lipodystrophy due to seipin as compared with 1-acylglycerol-3-phosphate-o-acyltransferase-2 deficiency.
Antuna-Puente B, Boutet E, Vigouroux C, Lascols O, Slama L, Caron-Debarle M, Khallouf E, Lévy-Marchal C, Capeau J, Bastard JP, Magré J. Antuna-Puente B, et al. Among authors: magre j. J Clin Endocrinol Metab. 2010 Mar;95(3):1463-8. doi: 10.1210/jc.2009-1824. Epub 2010 Jan 22. J Clin Endocrinol Metab. 2010. PMID: 20097706
[Primary lipodystrophies].
Capeau J, Magré J, Lascols O, Caron M, Béréziat V, Vigouroux C. Capeau J, et al. Among authors: magre j. Ann Endocrinol (Paris). 2007 Feb;68(1):10-20. doi: 10.1016/j.ando.2006.12.003. Epub 2007 Feb 21. Ann Endocrinol (Paris). 2007. PMID: 17320032 French.
[Diabetes and genetic and acquired lipodystrophy syndrome].
Capeau J, Magré J, Vigouroux C, Caron M, Maachi M, Dubosclard E, Lascols O, Bastard JP. Capeau J, et al. Among authors: magre j. Journ Annu Diabetol Hotel Dieu. 2003:99-109. Journ Annu Diabetol Hotel Dieu. 2003. PMID: 12868305 Review. French. No abstract available.
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy.
Vigouroux C, Magré J, Vantyghem MC, Bourut C, Lascols O, Shackleton S, Lloyd DJ, Guerci B, Padova G, Valensi P, Grimaldi A, Piquemal R, Touraine P, Trembath RC, Capeau J. Vigouroux C, et al. Among authors: magre j. Diabetes. 2000 Nov;49(11):1958-62. doi: 10.2337/diabetes.49.11.1958. Diabetes. 2000. PMID: 11078466
112 results