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You searched for: Author/Creator Varret, Mathilde

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2. Description of a Large Family with Autosomal Dominant Hypercholesterolemia Associated with the APOE p.Leu167del Mutation. Issue 1 (11th October 2012)

4. Exome Sequencing in Suspected Monogenic Dyslipidemias. (April 2015)

5. High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry. (October 2018)

6. High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry. (October 2018)

7. PCSK9 polymorphism in a Tunisian cohort: Identification of a new allele, L8, and association of allele L10 with reduced coronary heart disease risk. Issue 1 (February 2015)

8. Plasma PCSK9 and cardiovascular events in type 2 diabetes. (August 2017)

9. Plasma proprotein‐convertase‐subtilisin/kexin type 9 (PCSK9) and cardiovascular events in type 2 diabetes. Issue 4 (14th January 2018)

10. 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)