1. High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry. (October 2018) Authors: Angoulvant, D.; Béliard, S.; Benlian, P.; Boileau, C.; Boccara, F.; Bruckert, E.; Cariou, B.; Carreau, V.; Carrié, A.; Charrière, S.; Di Filippo, M.; Ducluzeau, P.H.; Dulong, S.; Durlach, V.; Farnier, M.; Ferrari, E.; Ferrières, J.; Gallo, A.; Girardet, J.P.; Hankard, R. Journal: Atherosclerosis Issue: Volume 277(2018) Page Start: 334 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome. Issue 1 (22nd November 2021) Authors: Zanoni, Paolo; Panteloglou, Grigorios; Othman, Alaa; Haas, Joel T.; Meier, Roger; Rimbert, Antoine; Futema, Marta; Abou Khalil, Yara; Norrelykke, Simon F.; Rzepiela, Andrzej J.; Stoma, Szymon; Stebler, Michael; van Dijk, Freerk; Wijers, Melinde; Wolters, Justina C.; Dalila, Nawar; Huijkman, Nicol... Journal: Circulation research Issue: Volume 130:Issue 1(2022) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Proprotein convertase subtilisin / kexin 9 (PCSK9) inhibitors and the future of dyslipidemia therapy: an updated patent review (2011-2015). (1st December 2016) Authors: Elbitar, Sandy; Khoury, Petra El; Ghaleb, Youmna; Rabès, Jean-Pierre; Varret, Mathilde; Seidah, Nabil G.; Boileau, Catherine; Abifadel, Marianne Journal: Expert opinion on therapeutic patents Issue: Volume 26:Number 12(2016:Dec.) Page Start: 1377 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. APOE gene variants in primary dyslipidemia. (July 2021) Authors: Khalil, Yara Abou; Rabès, Jean-Pierre; Boileau, Catherine; Varret, Mathilde Journal: Atherosclerosis Issue: Volume 328(2021) Page Start: 11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Polymorphisms rs2745557 in PTGS2 and rs2075797 in PTGER2 are associated with the risk of chronic obstructive pulmonary disease development in a Tunisian cohort. (March 2021) Authors: Mani, Salma; Norel, Xavier; Varret, Mathilde; Bchir, Sarra; ben Anes, Amel; Garrouch, Abdelahamid; Tabka, Zouhair; Longrois, Dan; Chahed, Karim Journal: Prostaglandins, leukotrienes, and essential fatty acids Issue: Volume 166(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry. (October 2018) Authors: Béliard, Sophie; Boccara, Franck; Cariou, Bertrand; Carrié, Alain; Collet, Xavier; Farnier, Michel; Ferrières, Jean; Krempf, Michael; Peretti, Noël; Rabès, Jean-Pierre; Varret, Mathilde; Vimont, Alexandre; Charrière, Sybil; Bruckert, Eric Journal: Atherosclerosis Issue: Volume 277(2018) Page Start: 334 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Plasma proprotein‐convertase‐subtilisin/kexin type 9 (PCSK9) and cardiovascular events in type 2 diabetes. Issue 4 (14th January 2018) Authors: El Khoury, Petra; Roussel, Ronan; Fumeron, Frederic; Abou‐Khalil, Yara; Velho, Gilberto; Mohammedi, Kamel; Jacob, Marie‐Paule; Steg, Philippe Gabriel; Potier, Louis; Ghaleb, Youmna; Elbitar, Sandy; Ragot, Stephanie; Andreata, Francesco; Caligiuri, Giusepinna; Hadjadj, Samy; Boileau, Catherine; Ma... Journal: Diabetes, obesity & metabolism Issue: Volume 20:Issue 4(2018) Page Start: 943 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Effect of the p.Arg357His mutation of PCSK9 on basal and postprandial lipoprotein metabolism. (August 2017) Authors: Varret, Mathilde; Abifadel, Marianne; Despina Kalopissis, Athina; Fatoumata Maiga, Sira; Lambert, Gilles; Seidah, Nabil G.; Boileau, Catherine; Chabert, Michele Journal: Atherosclerosis Issue: Volume 263(2017) Page Start: e2 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Description of a Large Family with Autosomal Dominant Hypercholesterolemia Associated with the APOE p.Leu167del Mutation. Issue 1 (11th October 2012) Authors: Marduel, Marie; Ouguerram, Khadija; Serre, Valérie; Bonnefont‐Rousselot, Dominique; Marques‐Pinheiro, Alice; Erik Berge, Knut; Devillers, Martine; Luc, Gérald; Lecerf, Jean‐Michel; Tosolini, Laurent; Erlich, Danièle; Peloso, Gina M.; Stitziel, Nathan; Nitchké, Patrick; Jaïs, Jean‐Philippe; Abifad... Journal: Human mutation Issue: Volume 34:Issue 1(2013:Jan.) Page Start: 83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Exome Sequencing in Suspected Monogenic Dyslipidemias. (April 2015) Authors: Stitziel, Nathan O.; Peloso, Gina M.; Abifadel, Marianne; Cefalu, Angelo B.; Fouchier, Sigrid; Motazacker, M. Mahdi; Tada, Hayato; Larach, Daniel B.; Awan, Zuhier; Haller, Jorge F.; Pullinger, Clive R.; Varret, Mathilde; Rabès, Jean-Pierre; Noto, Davide; Tarugi, Patrizia; Kawashiri, Masa-aki; Noh... Journal: Circulation Issue: Volume 8:Number 2(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗