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Journal of Clinical Lipidology|June 29, 2020
High prevalence of plasma lipid abnormalities in human and canine Duchenne and Becker muscular dystrophies depicts a new type of primary genetic dyslipidemiaZoe White, Chady H Hakim, Marine Theret, et al.Journal of Clinical Lipidology|May 10, 2023
The clinical effects of inclisiran, a first-in-class LDL-C lowering siRNA therapy, on the LDL-C levels in Chinese patients with hypercholesterolemiaZhu Luo, Zhijun Huang, Feng Sun, et al.Journal of Clinical Lipidology|September 27, 2012
Phenotypes of hypertriglyceridemia caused by excess very-low-density lipoproteinAllan D Sniderman, Andre Tremblay, Jacqueline De Graaf, et al.Journal of Clinical Lipidology|September 27, 2012
Hospital use and medical care costs up to 5 years after triglyceride lowering among patients with severe hypertriglyceridemiaGregory A Nichols, Bhakti Arondekar, Terry A JacobsonJournal of Clinical Lipidology|February 12, 2015
Fractional cholesterol absorption measurements in humans: determinants of the blood-based dual stable isotope tracer techniqueFrans Stellaard, Dieter LütjohannJournal of Clinical Lipidology|February 12, 2015
Changes in LDL particle concentrations after treatment with the cholesteryl ester transfer protein inhibitor anacetrapib alone or in combination with atorvastatinRonald M Krauss, Cathy Anne Pinto, Yang Liu, et al.Journal of Clinical Lipidology|February 12, 2015
Long-term clinical results of microsomal triglyceride transfer protein inhibitor use in a patient with homozygous familial hypercholesterolemiaAnna Raper, Daniel M Kolansky, Bruce S Sachais, et al.Journal of Clinical Lipidology|July 9, 2020
Autosomal recessive hypercholesterolemia in a kindred of Syrian ancestryMorten Hostrup Martinsen, Ib Christian Klausen, Anne Tybjaerg-Hansen, et al.Journal of Clinical Lipidology|August 12, 2022
Cost-effectiveness of population-wide genomic screening for familial hypercholesterolemia in the United StatesScott J Spencer, Laney K Jones, Gregory F Guzauskas, et al.Journal of Clinical Lipidology|August 9, 2022
Familial chylomicronemia syndrome. A sixty year follow-up in two siblings and their kindreds. Nosological and clinical considerationsGiovanni B Vigna, Nadia Citroni, Patrizia Tarugi, et al.Pageof 200