A Inazu|J Koizumi|H Mabuchi - JoVE Visualize

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Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1994

[CETP deficiency]A Inazu, J Koizumi, H Mabuchi

Rinsho Byori. the Japanese Journal of Clinical Pathology|May 1, 1993

[New approach to pathogenesis of genetic hyperlipoproteinemias]J Koizumi, A Inazu, H Mabuchi

Current Opinion in Lipidology|August 17, 2000

Cholesteryl ester transfer protein and atherosclerosisA Inazu, J Koizumi, H Mabuchi

Rinsho Byori. the Japanese Journal of Clinical Pathology|April 1, 1996

[Cholesteryl ester transfer protein (CETP) deficiency and increased HDL cholesterol levels (hyperalphalipoproteinemia)]A Inazu, J Koizumi, H Mabuchi

Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 1, 1992

Enhanced cholesteryl ester transfer protein activities and abnormalities of high density lipoproteins in familial hypercholesterolemiaA Inazu, J Koizumi, H Mabuchi, et al.

Atherosclerosis|July 25, 1997

Clinical characteristics of double heterozygotes with familial hypercholesterolemia and cholesteryl ester transfer protein deficiencyT Haraki, A Inazu, K Yagi, et al.

Atherosclerosis|September 17, 1999

Opposite effects on serum cholesteryl ester transfer protein levels between long-term treatments with pravastatin and probucol in patients with primary hypercholesterolemia and xanthomaA Inazu, J Koizumi, K Kajinami, et al.

The American Journal of Cardiology|July 22, 1998

Low-density lipoprotein receptor genotype-dependent response to cholesterol lowering by combined pravastatin and cholestyramine in familial hypercholesterolemiaK Kajinami, K Yagi, T Higashikata, et al.

Arteriosclerosis, Thrombosis, and Vascular Biology|August 14, 1999

Abetalipoproteinemia caused by maternal isodisomy of chromosome 4q containing an intron 9 splice acceptor mutation in the microsomal triglyceride transfer protein geneX P Yang, A Inazu, K Yagi, et al.

The American Journal of Cardiology|October 12, 2000

Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemiaM Kawashiri, K Kajinami, A Nohara, et al.

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Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1994

[CETP deficiency]A Inazu, J Koizumi, H Mabuchi

Rinsho Byori. the Japanese Journal of Clinical Pathology|May 1, 1993

[New approach to pathogenesis of genetic hyperlipoproteinemias]J Koizumi, A Inazu, H Mabuchi

Current Opinion in Lipidology|August 17, 2000

Cholesteryl ester transfer protein and atherosclerosisA Inazu, J Koizumi, H Mabuchi

Rinsho Byori. the Japanese Journal of Clinical Pathology|April 1, 1996

[Cholesteryl ester transfer protein (CETP) deficiency and increased HDL cholesterol levels (hyperalphalipoproteinemia)]A Inazu, J Koizumi, H Mabuchi

Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 1, 1992

Enhanced cholesteryl ester transfer protein activities and abnormalities of high density lipoproteins in familial hypercholesterolemiaA Inazu, J Koizumi, H Mabuchi, et al.

Atherosclerosis|July 25, 1997

Clinical characteristics of double heterozygotes with familial hypercholesterolemia and cholesteryl ester transfer protein deficiencyT Haraki, A Inazu, K Yagi, et al.

Atherosclerosis|September 17, 1999

Opposite effects on serum cholesteryl ester transfer protein levels between long-term treatments with pravastatin and probucol in patients with primary hypercholesterolemia and xanthomaA Inazu, J Koizumi, K Kajinami, et al.

The American Journal of Cardiology|July 22, 1998

Low-density lipoprotein receptor genotype-dependent response to cholesterol lowering by combined pravastatin and cholestyramine in familial hypercholesterolemiaK Kajinami, K Yagi, T Higashikata, et al.

Arteriosclerosis, Thrombosis, and Vascular Biology|August 14, 1999

Abetalipoproteinemia caused by maternal isodisomy of chromosome 4q containing an intron 9 splice acceptor mutation in the microsomal triglyceride transfer protein geneX P Yang, A Inazu, K Yagi, et al.

The American Journal of Cardiology|October 12, 2000

Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemiaM Kawashiri, K Kajinami, A Nohara, et al.

Pageof 30