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Alterations in plasma triglycerides lipolysis in patients with history of multifactorial chylomicronemia.
Atherosclerosis. 2017 Oct;265:22-28. doi: 10.1016/j.atherosclerosis.2017.07.030. Epub 2017 Jul 29.
Atherosclerosis. 2017.
PMID: 28829998
New rare genetic variants of LMF1 gene identified in severe hypertriglyceridemia.
Serveaux Dancer M, Di Filippo M, Marmontel O, Valéro R, Piombo Rivarola MDC, Peretti N, Caussy C, Krempf M, Vergès B, Mahl M, Marçais C, Moulin P, Charrière S.
Serveaux Dancer M, et al.
J Clin Lipidol. 2018 Sep-Oct;12(5):1244-1252. doi: 10.1016/j.jacl.2018.06.018. Epub 2018 Jul 7.
J Clin Lipidol. 2018.
PMID: 30037590
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Involvement of a homozygous exon 6 deletion of LMF1 gene in intermittent severe hypertriglyceridemia.
Serveaux Dancer M, Marmontel O, Wozny AS, Marcais C, Mahl M, Dumont S, Simonet T, Moulin P, Di Filippo M, Charrière S.
Serveaux Dancer M, et al.
J Clin Lipidol. 2020 Nov-Dec;14(6):756-761. doi: 10.1016/j.jacl.2020.09.004. Epub 2020 Sep 18.
J Clin Lipidol. 2020.
PMID: 33039347
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Pathological Implications of Receptor for Advanced Glycation End-Product (AGER) Gene Polymorphism.
Serveaux-Dancer M, Jabaudon M, Creveaux I, Belville C, Blondonnet R, Gross C, Constantin JM, Blanchon L, Sapin V.
Serveaux-Dancer M, et al.
Dis Markers. 2019 Feb 4;2019:2067353. doi: 10.1155/2019/2067353. eCollection 2019.
Dis Markers. 2019.
PMID: 30863465
Free PMC article.
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