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Looking at New Unexpected Disease Targets in LMNA-Linked Lipodystrophies in the Light of Complex Cardiovascular Phenotypes: Implications for Clinical Practice.
Mosbah H, Vatier C, Boccara F, Jéru I, Lascols O, Vantyghem MC, Fève B, Donadille B, Sarrazin E, Benabbou S, Inamo J, Ederhy S, Cohen A, Neraud B, Richard P, Picard F, Christin-Maitre S, Redheuil A, Wahbi K, Vigouroux C. Mosbah H, et al. Among authors: vigouroux c. Cells. 2020 Mar 20;9(3):765. doi: 10.3390/cells9030765. Cells. 2020. PMID: 32245113 Free PMC article.
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. Diabetes. 2000 Nov;49(11):1958-62. doi: 10.2337/diabetes.49.11.1958. Diabetes. 2000. PMID: 11078466
A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy.
Caux F, Dubosclard E, Lascols O, Buendia B, Chazouillères O, Cohen A, Courvalin JC, Laroche L, Capeau J, Vigouroux C, Christin-Maitre S. Caux F, et al. Among authors: vigouroux c. J Clin Endocrinol Metab. 2003 Mar;88(3):1006-13. doi: 10.1210/jc.2002-021506. J Clin Endocrinol Metab. 2003. PMID: 12629077
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. Among authors: vigouroux c. Diabetes. 2003 Jun;52(6):1573-8. doi: 10.2337/diabetes.52.6.1573. Diabetes. 2003. PMID: 12765973
[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: vigouroux c. Journ Annu Diabetol Hotel Dieu. 2003:99-109. Journ Annu Diabetol Hotel Dieu. 2003. PMID: 12868305 Review. French. No abstract available.
LMNA mutations in atypical Werner's syndrome.
Vigouroux C, Caux F, Capeau J, Christin-Maitre S, Cohen A. Vigouroux C, et al. Lancet. 2003 Nov 8;362(9395):1585; author reply 1586. doi: 10.1016/S0140-6736(03)14760-5. Lancet. 2003. PMID: 14615128 No abstract available.
A-type lamin-linked lipodystrophies.
Vigouroux C, Capeau J. Vigouroux C, et al. Novartis Found Symp. 2005;264:166-77; discussion 177-82, 227-30. Novartis Found Symp. 2005. PMID: 15773753 Review.
201 results