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1. Characterization of Autosomal Dominant Hypercholesterolemia Caused by PCSK9 Gain of Function Mutations and Its Specific Treatment With Alirocumab, a PCSK9 Monoclonal Antibody. (December 2015)

2. ClinVar database of global familial hypercholesterolemia‐associated DNA variants. Issue 11 (11th October 2018)

3. Corrigendum to "Phospholipid transfer to high-density lipoprotein (HDL) upon triglyceride lipolysis is directly correlated with HDL-cholesterol levels and is not associated with cardiovascular risk" [Atherosclerosis 324C (2021) 1–8]. (May 2023)

5. Genetic testing of familial hypercholesterolemia: Monogenic form and polygenic contribution to cardiovascular risk. (August 2017)

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

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

9. Long-term outcome in 53 patients with homozygous familial hypercholesterolaemia in a single centre in France. (February 2017)

10. Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in Adulthood. Issue 2 (29th December 2022)