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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
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
[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.
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
112 results