Lv2
110 积分 2021-07-23 加入
A novel splicing variant in ABCA1 in the first reported Hong Kong Chinese patient with high-density lipoprotein deficiency
15天前
已关闭
IgG3κ Monoclonal Membranous Nephropathy Associated With Acquired Lecithin Cholesterol Acyltransferase Deficiency
15天前
已关闭
Novel therapeutic opportunities for familial lecithin:cholesterol acyltransferase deficiency: promises and challenges
16天前
已完结
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review
16天前
已完结
Risk of Atherosclerotic Cardiovascular Disease in Familial Remnant Hyperlipidemia (Dysbetalipoproteinemia) and Familial Hypercholesterolemia
17天前
已关闭
Characterization of Familial Chylomicronemia Syndrome in a Compound Heterozygote for Two APOA5 Nonsense Variants
19天前
已关闭
Contribution of APOE Genetic Variants to Dyslipidemia
19天前
已完结
An Updated Review of Novel Triglyceride-Lowering Therapies in Adults with Familial Chylomicronemia Syndrome
19天前
已完结
Olezarsen for the Treatment of Familial Chylomicronemia Syndrome
19天前
已完结
Polygenic risk in Type III hyperlipidaemia and risk of cardiovascular disease: An epidemiological study in UK Biobank and Oxford Biobank
19天前
已完结
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