A Resuscitated Case of Acute Myocardial Infarction with both Familial Hypercholesterolemia Phenotype Caused by Possibly Oligogenic Variants of the <i>PCSK9</i> and <i>ABCG5</i> Genes and Type I CD36 Deficiency

Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery Disease

(2020) Akihiro Nomura et al.   Circulation-Genomic and Precision Medicine

Rare and Deleterious Mutations in ABCG5/ABCG8 Genes Contribute to Mimicking and Worsening of Familial Hypercholesterolemia Phenotype

(2019) Hayato Tada et al.   CIRCULATION JOURNAL

Impact of LDLR and PCSK9 pathogenic variants in Japanese heterozygous familial hypercholesterolemia patients

(2019) Mika Hori et al.   ATHEROSCLEROSIS

Reference Intervals of Serum Non-Cholesterol Sterols by Gender in Healthy Japanese Individuals

(2019) Hiroshi Yoshida et al.   Journal of Atherosclerosis and Thrombosis

Guidance for Pediatric Familial Hypercholesterolemia 2017

(2018) Mariko Harada-Shiba et al.   Journal of Atherosclerosis and Thrombosis

Guidelines for Diagnosis and Treatment of Familial Hypercholesterolemia 2017

(2018) Mariko Harada-Shiba et al.   Journal of Atherosclerosis and Thrombosis

Sitosterolemia, Hypercholesterolemia, and Coronary Artery Disease

(2018) Hayato Tada et al.   Journal of Atherosclerosis and Thrombosis

Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease

(2018) Hayato Tada et al.   Journal of Clinical Lipidology

Clinical Genetic Testing for Familial Hypercholesterolemia

(2018) Amy C. Sturm et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Independent Link Between Levels of Proprotein Convertase Subtilisin/Kexin Type 9 and FABP4 in a General Population Without Medication

(2016) Masato Furuhashi et al.   AMERICAN JOURNAL OF CARDIOLOGY

Prevalence of Familial Hypercholesterolemia in the 1999 to 2012 United States National Health and Nutrition Examination Surveys (NHANES)CLINICAL PERSPECTIVE

(2016) Sarah D. de Ferranti et al.   CIRCULATION

Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

(2016) Amit V. Khera et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Prevalence and management of familial hypercholesterolaemia in patients with acute coronary syndromes

(2015) David Nanchen et al.   EUROPEAN HEART JOURNAL

Proprotein Convertase Subtilisin Kexin Type 9 Promotes Intestinal Overproduction of Triglyceride-Rich Apolipoprotein B Lipoproteins Through Both Low-Density Lipoprotein Receptor–Dependent and –Independent Mechanisms

(2014) Shirya Rashid et al.   CIRCULATION

Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society

(2013) B. G. Nordestgaard et al.   EUROPEAN HEART JOURNAL

Patients with CD36 Deficiency Are Associated with Enhanced Atherosclerotic Cardiovascular Diseases

(2011) Miyako Yuasa-Kawase et al.   Journal of Atherosclerosis and Thrombosis

Chylomicron remnants are increased in the postprandial state in CD36 deficiency

(2008) Daisaku Masuda et al.   JOURNAL OF LIPID RESEARCH

Genetic variants in PCSK9 in the Japanese population: Rare genetic variants in PCSK9 might collectively contribute to plasma LDL cholesterol levels in the general population

(2007) Yasuko Miyake et al.   ATHEROSCLEROSIS