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Page 1
Cardiometabolic assessment of lamin A/C gene mutation carriers: a phenotype-genotype correlation.
Kwapich M, Lacroix D, Espiard S, Ninni S, Brigadeau F, Kouakam C, Degroote P, Laurent JM, Tiffreau V, Jannin A, Humbert L, Ben Hamou A, Tard C, Ben Yaou R, Lamblin N, Klug D, Richard P, Vigouroux C, Bonne G, Vantyghem MC; Diamenord–AEDNL Working Group. Kwapich M, et al. Among authors: vantyghem mc. Diabetes Metab. 2019 Sep;45(4):382-389. doi: 10.1016/j.diabet.2018.09.006. Epub 2018 Oct 1. Diabetes Metab. 2019. PMID: 30287275
Irisin levels in LMNA-associated partial lipodystrophies.
Bensmaïne F, Benomar K, Espiard S, Vahe C, Le Mapihan K, Lion G, Lemdani M, Chazard E, Ernst O, Vigouroux C, Pigny P, Vantyghem MC. Bensmaïne F, et al. Among authors: vantyghem mc. Diabetes Metab. 2019 Jan;45(1):67-75. doi: 10.1016/j.diabet.2018.08.003. Epub 2018 Aug 27. Diabetes Metab. 2019. PMID: 30165155
One-year metreleptin improves insulin secretion in patients with diabetes linked to genetic lipodystrophic syndromes.
Vatier C, Fetita S, Boudou P, Tchankou C, Deville L, Riveline J, Young J, Mathivon L, Travert F, Morin D, Cahen J, Lascols O, Andreelli F, Reznik Y, Mongeois E, Madelaine I, Vantyghem M, Gautier J, Vigouroux C. Vatier C, et al. Among authors: vantyghem m. Diabetes Obes Metab. 2016 Jul;18(7):693-7. doi: 10.1111/dom.12606. Epub 2016 Jan 12. Diabetes Obes Metab. 2016. PMID: 26584826
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: vantyghem mc. Diabetes. 2000 Nov;49(11):1958-62. doi: 10.2337/diabetes.49.11.1958. Diabetes. 2000. PMID: 11078466
Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins).
Mosbah H, Donadille B, Vatier C, Janmaat S, Atlan M, Badens C, Barat P, Béliard S, Beltrand J, Ben Yaou R, Bismuth E, Boccara F, Cariou B, Chaouat M, Charriot G, Christin-Maitre S, De Kerdanet M, Delemer B, Disse E, Dubois N, Eymard B, Fève B, Lascols O, Mathurin P, Nobécourt E, Poujol-Robert A, Prevost G, Richard P, Sellam J, Tauveron I, Treboz D, Vergès B, Vermot-Desroches V, Wahbi K, Jéru I, Vantyghem MC, Vigouroux C. Mosbah H, et al. Among authors: vantyghem mc. Orphanet J Rare Dis. 2022 Apr 19;17(Suppl 1):170. doi: 10.1186/s13023-022-02308-7. Orphanet J Rare Dis. 2022. PMID: 35440056 Free PMC article.
280 results