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Sitosterolemia, Hypercholesterolemia, and Coronary Artery Disease

Journal of Atherosclerosis and Thrombosis, 2018/09/01, Vol.25(9), pp.783-789

2018

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HDL3 Cholesterol Levels in an Elderly Population

Journal of Atherosclerosis and Thrombosis, 2018/01/01, Vol.25(1), pp.40-41

Inazu, Akihiro

2018

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Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease

Journal of clinical lipidology, 2018-11, Vol.12 (6), p.1436-1444

2018

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Post-prandial Remnant Lipoprotein Metabolism in Sitosterolemia

Journal of Atherosclerosis and Thrombosis, 2018/12/01, Vol.25(12), pp.1188-1195

2018

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Cholesteryl ester transfer protein (CETP) deficiency and CETP inhibitors

Molecules and Cells, 2014, 37(11), , pp.777-784

2014

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Lipid Management in a Japanese Community:Attainment Rate of Target Set by the Japan Atherosclerosis Society Guidelines for the Prevention of Atherosclerotic Cardiovascular Diseases 2012

Journal of Atherosclerosis and Thrombosis, 2017/03/01, Vol.24(3), pp.338-345

2017

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Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease

Circulation research, 2017-06, Vol.121 (1), p.81-88

2017

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Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 ( PCSK9 ) gain-of-function mutation

Atherosclerosis, 2014-09, Vol.236 (1), p.54-61

2014

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Remnant-like particles and coronary artery disease in familial hypercholesterolemia

Clinica chimica acta, 2018-07, Vol.482, p.120-123

2018

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Lipoprotein(a) in Familial Hypercholesterolemia With Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Gain-of-Function Mutations

Circulation Journal, 2016/01/25, Vol.80(2), pp.512-518

2016

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A Rare Coincidence of Sitosterolemia and Familial Mediterranean Fever Identified by Whole Exome Sequencing

Journal of Atherosclerosis and Thrombosis, 2016/07/01, Vol.23(7), pp.884-890

2016

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Impact of evolocumab treatment on low-density lipoprotein cholesterol levels in heterozygous familial hypercholesterolemic patients withdrawing from regular apheresis

Atherosclerosis, 2017-10, Vol.265, p.225-230

2017

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Assessment of Coronary Atherosclerosis in Patients With Familial Hypercholesterolemia by Coronary Computed Tomography Angiography

The American journal of cardiology, 2015-03, Vol.115 (6), p.724-729

2015

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Molecular and functional characterization of familial chylomicronemia syndrome

Atherosclerosis, 2018-02, Vol.269, p.272-278

2018

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Genetic Association between Lipid-Regulating Drug Targets and Diabetic Retinopathy: A Drug Target Mendelian Randomization Study

Journal of lipids, 2024-05, Vol.2024, p.5324127-10

2024

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Putative Pathogenic Variants of ABCG5 and ABCG8 of Sitosterolemia in Patients With Hyper-Low-Density Lipoprotein Cholesterolemia

지질·동맥경화학회지, 2024, 13(1), , pp.53-60

2024

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The E32K variant of PCSK9 exacerbates the phenotype of familial hypercholesterolaemia by increasing PCSK9 function and concentration in the circulation

Atherosclerosis, 2010-05, Vol.210 (1), p.166-172

2010

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Hypolipidemic effect of Pleurotus eryngii extract in fat-loaded mice

Journal of Nutritional Science and Vitaminology, 2010, Vol.56(1), pp.48-53

2010

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Autosomal Recessive Hypercholesterolemia: A Mild Phenotype of Familial Hypercholesterolemia: Insight from the Kinetic Study using Stable Isotope and Animal Studies

Journal of Atherosclerosis and Thrombosis, 2015/01/26, Vol.22(1), pp.1-9

2015

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Impacts of Visceral Adipose Tissue and Subcutaneous Adipose Tissue on Metabolic Risk Factors in Middle-aged Japanese

Obesity (Silver Spring, Md.), 2010-01, Vol.18 (1), p.153-160

2010

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Efficacy and Safety of Coadministration of Rosuvastatin , Ezetimibe , and Colestimide in Heterozygous Familial Hypercholesterolemia

The American journal of cardiology, 2012-02, Vol.109 (3), p.364-369

2012

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HDL3 Cholesterol Levels in an Elderly Population

Journal of Atherosclerosis and Thrombosis, 2018, Vol.25 (1), p.40-41

Akihiro Inazu

2018

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A novel type of familial hypercholesterolemia: Double heterozygous mutations in LDL receptor and LDL receptor adaptor protein 1 gene

Atherosclerosis, 2011-12, Vol.219 (2), p.663-666

2011

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A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencing

Clinica chimica acta, 2016-01, Vol.453, p.194-196

2016

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Cholesteryl Ester Transfer Protein (CETP) Deficiency and CETP Inhibitors

Molecules and cells, 2014-11, Vol.37 (11), p.777-784

2014

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Sitosterolemia, Hypercholesterolemia, and Coronary Artery Disease

HDL3 Cholesterol Levels in an Elderly Population

Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease

Post-prandial Remnant Lipoprotein Metabolism in Sitosterolemia

Cholesteryl ester transfer protein (CETP) deficiency and CETP inhibitors

Lipid Management in a Japanese Community:Attainment Rate of Target Set by the Japan Atherosclerosis Society Guidelines for the Prevention of Atherosclerotic Cardiovascular Diseases 2012

Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease

Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 ( PCSK9 ) gain-of-function mutation

Remnant-like particles and coronary artery disease in familial hypercholesterolemia

Lipoprotein(a) in Familial Hypercholesterolemia With Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Gain-of-Function Mutations

A Rare Coincidence of Sitosterolemia and Familial Mediterranean Fever Identified by Whole Exome Sequencing

Impact of evolocumab treatment on low-density lipoprotein cholesterol levels in heterozygous familial hypercholesterolemic patients withdrawing from regular apheresis

Assessment of Coronary Atherosclerosis in Patients With Familial Hypercholesterolemia by Coronary Computed Tomography Angiography

Molecular and functional characterization of familial chylomicronemia syndrome

Genetic Association between Lipid-Regulating Drug Targets and Diabetic Retinopathy: A Drug Target Mendelian Randomization Study

Putative Pathogenic Variants of ABCG5 and ABCG8 of Sitosterolemia in Patients With Hyper-Low-Density Lipoprotein Cholesterolemia

The E32K variant of PCSK9 exacerbates the phenotype of familial hypercholesterolaemia by increasing PCSK9 function and concentration in the circulation

Hypolipidemic effect of Pleurotus eryngii extract in fat-loaded mice

Autosomal Recessive Hypercholesterolemia: A Mild Phenotype of Familial Hypercholesterolemia: Insight from the Kinetic Study using Stable Isotope and Animal Studies

Impacts of Visceral Adipose Tissue and Subcutaneous Adipose Tissue on Metabolic Risk Factors in Middle-aged Japanese

Efficacy and Safety of Coadministration of Rosuvastatin , Ezetimibe , and Colestimide in Heterozygous Familial Hypercholesterolemia

HDL3 Cholesterol Levels in an Elderly Population

A novel type of familial hypercholesterolemia: Double heterozygous mutations in LDL receptor and LDL receptor adaptor protein 1 gene

A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencing

Cholesteryl Ester Transfer Protein (CETP) Deficiency and CETP Inhibitors

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