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You searched for: Author/Creator Rabès, Jean-Pierre

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

3. 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. Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome. Issue 1 (22nd November 2021)

9. Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome. Issue 1 (7th January 2022)

10. Proprotein convertase subtilisin / kexin 9 (PCSK9) inhibitors and the future of dyslipidemia therapy: an updated patent review (2011-2015). (1st December 2016)