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Page 1
Molecular spectrum of autosomal dominant hypercholesterolemia in France.
Marduel M, Carrié A, Sassolas A, Devillers M, Carreau V, Di Filippo M, Erlich D, Abifadel M, Marques-Pinheiro A, Munnich A, Junien C; French ADH Research Network; Boileau C, Varret M, Rabès JP. Marduel M, et al. Among authors: carreau v. Hum Mutat. 2010 Nov;31(11):E1811-24. doi: 10.1002/humu.21348. Hum Mutat. 2010. PMID: 20809525 Free PMC article.
Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia.
Marmontel O, Abou-Khalil Y, Bluteau O, Cariou B, Carreau V, Charrière S, Divry E, Gallo A, Moulin P, Paillard F, Peretti N, Rabès JP, Varret M, Carrié A, Di Filippo M. Marmontel O, et al. Among authors: carreau v. Arterioscler Thromb Vasc Biol. 2023 Jul;43(7):e270-e278. doi: 10.1161/ATVBAHA.123.319146. Epub 2023 Apr 27. Arterioscler Thromb Vasc Biol. 2023. PMID: 37128917
Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome.
Zanoni P, Panteloglou G, Othman A, Haas JT, Meier R, Rimbert A, Futema M, Abou Khalil Y, Norrelykke SF, Rzepiela AJ, Stoma S, Stebler M, van Dijk F, Wijers M, Wolters JC, Dalila N, Huijkman NCA, Smit M, Gallo A, Carreau V, Philippi A, Rabès JP, Boileau C, Visentin M, Vonghia L, Weyler J, Francque S, Verrijken A, Verhaegen A, Van Gaal L, van der Graaf A, van Rosmalen BV, Robert J, Velagapudi S, Yalcinkaya M, Keel M, Radosavljevic S, Geier A, Tybjaerg-Hansen A, Varret M, Rohrer L, Humphries SE, Staels B, van de Sluis B, Kuivenhoven JA, von Eckardstein A. Zanoni P, et al. Among authors: carreau v. Circ Res. 2022 Jan 7;130(1):80-95. doi: 10.1161/CIRCRESAHA.120.318141. Epub 2021 Nov 23. Circ Res. 2022. PMID: 34809444 Free article.
APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia.
Abou Khalil Y, Marmontel O, Ferrières J, Paillard F, Yelnik C, Carreau V, Charrière S, Bruckert E, Gallo A, Giral P, Philippi A, Bluteau O, Boileau C, Abifadel M, Di-Filippo M, Carrié A, Rabès JP, Varret M. Abou Khalil Y, et al. Among authors: carreau v. Int J Mol Sci. 2022 May 21;23(10):5792. doi: 10.3390/ijms23105792. Int J Mol Sci. 2022. PMID: 35628605 Free PMC article.
Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia.
Ghaleb Y, Elbitar S, Philippi A, El Khoury P, Azar Y, Andrianirina M, Loste A, Abou-Khalil Y, Nicolas G, Le Borgne M, Moulin P, Di-Filippo M, Charrière S, Farnier M, Yelnick C, Carreau V, Ferrières J, Lecerf JM, Derksen A, Bernard G, Gauthier MS, Coulombe B, Lütjohann D, Fin B, Boland A, Olaso R, Deleuze JF, Rabès JP, Boileau C, Abifadel M, Varret M. Ghaleb Y, et al. Among authors: carreau v. Metabolites. 2022 Mar 18;12(3):262. doi: 10.3390/metabo12030262. Metabolites. 2022. PMID: 35323704 Free PMC article.
Burden of cardiovascular disease in a large contemporary cohort of patients with heterozygous familial hypercholesterolemia.
Ferrières J, Farnier M, Bruckert E, Vimont A, Durlach V, Ferrari E, Gallo A, Boccara F, Ferrières D, Béliard S; French FH Registry group: French REgistry of Familial hypERCHOLesterolemia (REFERCHOL). Ferrières J, et al. Atheroscler Plus. 2022 Aug 17;50:17-24. doi: 10.1016/j.athplu.2022.08.001. eCollection 2022 Dec. Atheroscler Plus. 2022. PMID: 36643794 Free PMC article.
Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in Adulthood.
Mourre F, Giorgi R, Gallo A, Boccara F, Bruckert E, Carrié A, Hankard R, Inamo J, Laboureau S, Moulin P, Valéro R, Béliard S; REFERCHOL Investigators. Mourre F, et al. Arterioscler Thromb Vasc Biol. 2023 Feb;43(2):e94-e103. doi: 10.1161/ATVBAHA.122.318119. Epub 2022 Dec 29. Arterioscler Thromb Vasc Biol. 2023. PMID: 36579650 Free article.
36 results