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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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Development of quality indicators for care of chronic kidney disease in the primary care setting using electronic health data: a RAND-modified Delphi method

Clinical and experimental nephrology, 2017-04, Vol.21 (2), p.247-256

2017

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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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Reduction of Serum Ubiquinol-10 and Ubiquinone-10 Levels by Atorvastatin in Hypercholesterolemic Patients

Journal of Atherosclerosis and Thrombosis, 2005, Vol.12(2), pp.111-119

2005

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Global Anthropology versus Anthropologies: Comment

American anthropologist, 2016-12, Vol.118 (4), p.857-858

Koizumi, Junji

2016

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Global Anthropology versus Anthropologies

American anthropologist, 2016-12, Vol.118 (4), p.857-858

Koizumi, Junji

2016

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Mentoring the next generation of physician-scientists in Japan: a cross-sectional survey of mentees in six academic medical centers

BMC medical education, 2015-03, Vol.15 (1), p.54-54, Article 54

2015

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Identification of a Novel Missense Mutation in the Sterol 27-Hydroxylase Gene in Two Japanese Patients with Cerebrotendinous Xanthomatosis

Internal Medicine, 2010, Vol.49(12), pp.1127-1131

2010

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Long-term efficacy of low-density lipoprotein apheresis on coronary heart disease in familial hypercholesterolemia

The American journal of cardiology, 1998-12, Vol.82 (12), p.1489-1495

1998

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Serum lipoprotein lipase mass: Clinical significance of its measurement

Clinica chimica acta, 2007-03, Vol.378 (1), p.7-12

2007

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ATP-binding cassette transporter G8 M429V polymorphism as a novel genetic marker of higher cholesterol absorption in hypercholesterolaemic Japanese subjects

Clinical science (1979), 2005-08, Vol.109 (2), p.183

2005

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Diabetes Progression from "High-Normal" Glucose in School Teachers

Internal Medicine, 2010, Vol.49(13), pp.1271-1276

2010

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Extreme Contrast of Postprandial Remnant-Like Particles Formed in Abetalipoproteinemia and Homozygous Familial Hypobetalipoproteinemia

JIMD Reports, Volume 22, 2015-01, Vol.22, p.85-94

2015

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Efficacy of Colestimide Coadministered With Atorvastatin in Japanese Patients With Heterozygous Familial Hypercholesterolemia (FH)

Circulation Journal, 2005, Vol.69(5), pp.515-520

2005

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Effects of NK-104, a new hydroxymethylglutaryl-coenzyme reductase inhibitor, on low-density lipoprotein cholesterol in heterozygous familial hypercholesterolemia

The American journal of cardiology, 2000-01, Vol.85 (2), p.178-183

2000

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Increased High-Density Lipoprotein Levels Caused by a Common Cholesteryl-Ester Transfer Protein Gene Mutation

The New England journal of medicine, 1990-11, Vol.323 (18), p.1234-1238

1990

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Molecular genetic epidemiology of homozygous familial hypercholesterolemia in the Hokuriku district of Japan

Atherosclerosis, 2011-02, Vol.214 (2), p.404-407

2011

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Type III Hyperlipoproteinemia Exaggerated by Sheehan's Syndrome With Advanced Systemic Atherosclerosis: A 28-Year Clinical Course

Circulation Journal, 2005, Vol.69(6), pp.746-751

2005

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Cutoff Point Separating Affected and Unaffected Familial Hypercholesterolemic Patients Validated by LDL-receptor Gene Mutants

Journal of Atherosclerosis and Thrombosis, 2005, Vol.12(1), pp.35-40

2005

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Effects of CoQ10 supplementation on plasma lipoprotein lipid, CoQ10 and liver and muscle enzyme levels in hypercholesterolemic patients treated with atorvastatin: A randomized double-blind study

Atherosclerosis, 2007-12, Vol.195 (2), p.e182-e189

2007

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Abetalipoproteinemia caused by maternal isodisomy of chromosome 4q containing an intron 9 splice acceptor mutation in the microsomal triglyceride transfer protein gene

Arteriosclerosis, thrombosis, and vascular biology, 1999-08, Vol.19 (8), p.1950

1999

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Cholesterol-Years Score is Associated with Development of Senile Degenerative Aortic Stenosis in Heterozygous Familial Hypercholesterolemia

Journal of Atherosclerosis and Thrombosis, 2006, Vol.13(6), pp.323-328

2006

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Diabetes in the elderly

Nihon Rōnen Igakkai zasshi, 2010, Vol.47 (5), p.415-418

Koizumi, Junji

2010

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Abstract 20174: Impact of Entrance Examination on Development of Nonalcoholic Fatty Liver Disease in New University Students

Circulation (New York, N.Y.), 2015-11, Vol.132 (Suppl_3 Suppl 3), p.A20174-A20174

2015

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Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemia

The American journal of cardiology, 2000-10, Vol.86 (8), p.840-845

2000

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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

Development of quality indicators for care of chronic kidney disease in the primary care setting using electronic health data: a RAND-modified Delphi method

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

Reduction of Serum Ubiquinol-10 and Ubiquinone-10 Levels by Atorvastatin in Hypercholesterolemic Patients

Global Anthropology versus Anthropologies: Comment

Global Anthropology versus Anthropologies

Mentoring the next generation of physician-scientists in Japan: a cross-sectional survey of mentees in six academic medical centers

Identification of a Novel Missense Mutation in the Sterol 27-Hydroxylase Gene in Two Japanese Patients with Cerebrotendinous Xanthomatosis

Long-term efficacy of low-density lipoprotein apheresis on coronary heart disease in familial hypercholesterolemia

Serum lipoprotein lipase mass: Clinical significance of its measurement

ATP-binding cassette transporter G8 M429V polymorphism as a novel genetic marker of higher cholesterol absorption in hypercholesterolaemic Japanese subjects

Diabetes Progression from "High-Normal" Glucose in School Teachers

Extreme Contrast of Postprandial Remnant-Like Particles Formed in Abetalipoproteinemia and Homozygous Familial Hypobetalipoproteinemia

Efficacy of Colestimide Coadministered With Atorvastatin in Japanese Patients With Heterozygous Familial Hypercholesterolemia (FH)

Effects of NK-104, a new hydroxymethylglutaryl-coenzyme reductase inhibitor, on low-density lipoprotein cholesterol in heterozygous familial hypercholesterolemia

Increased High-Density Lipoprotein Levels Caused by a Common Cholesteryl-Ester Transfer Protein Gene Mutation

Molecular genetic epidemiology of homozygous familial hypercholesterolemia in the Hokuriku district of Japan

Type III Hyperlipoproteinemia Exaggerated by Sheehan's Syndrome With Advanced Systemic Atherosclerosis: A 28-Year Clinical Course

Cutoff Point Separating Affected and Unaffected Familial Hypercholesterolemic Patients Validated by LDL-receptor Gene Mutants

Effects of CoQ10 supplementation on plasma lipoprotein lipid, CoQ10 and liver and muscle enzyme levels in hypercholesterolemic patients treated with atorvastatin: A randomized double-blind study

Abetalipoproteinemia caused by maternal isodisomy of chromosome 4q containing an intron 9 splice acceptor mutation in the microsomal triglyceride transfer protein gene

Cholesterol-Years Score is Associated with Development of Senile Degenerative Aortic Stenosis in Heterozygous Familial Hypercholesterolemia

Diabetes in the elderly

Abstract 20174: Impact of Entrance Examination on Development of Nonalcoholic Fatty Liver Disease in New University Students

Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemia

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