R. Takeda

发表

Development of coronary heart disease in familial hypercholesterolemia.

H. Mabuchi, J. Koizumi, M. Shimizu, 1989, Circulation.

Genetic cholesteryl ester transfer protein deficiency caused by two prevalent mutations as a major determinant of increased levels of high density lipoprotein cholesterol.

H. Mabuchi, X. Jiang, Akihiro Inazu, 1994, The Journal of clinical investigation.

Serum lipid and lipoprotein levels in Japanese patients with familial hypercholesterolemia.

H. Mabuchi, J. Koizumi, K. Ueda, 1979, Atherosclerosis.

Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia.

H. Mabuchi, J. Koizumi, K. Ueda, 1985, Atherosclerosis.

Effects of CS-514 on serum lipoprotein lipid and apolipoprotein levels in patients with familial hypercholesterolemia.

H. Mabuchi, T. Wakasugi, K. Kajinami, 1987, Metabolism: clinical and experimental.

Removal of apolipoprotein E-enriched high density lipoprotein by LDL-apheresis in familial hypercholesterolaemia: a possible activation of the reverse cholesterol transport system.

H. Mabuchi, Akihiro Inazu, J. Koizumi, 1988, Atherosclerosis.

Abdominal Aortic Aneurysms in Familial Hypercholesterolemia—Case Reports

H. Mabuchi, J. Koizumi, M. Shimizu, 1993, Angiology.

Coronary ectasia in a homozygous patient with familial hypercholesterolemia.

H. Mabuchi, T. Ikawa, I. Michishita, 1986, Atherosclerosis.

Inhibition effect of quinaldic acid on glucose-induced insulin release from isolated Langerhans islets of the rat.

H. Mabuchi, S. Miyamoto, R. Takeda, 1974, Biochemical and biophysical research communications.

Insulin-releasing effect of quinaldic acid and its relatives on isolated Langerhans islets.

H. Mabuchi, S. Miyamoto, Y. Yoneyama, 1973, Biochemical and biophysical research communications.

Effect of an inhibitor of 3-hydroxy-3-methyglutaryl coenzyme A reductase on serum lipoproteins and ubiquinone-10-levels in patients with familial hypercholesterolemia.

H. Mabuchi, J. Koizumi, S. Miyamoto, 1981, The New England journal of medicine.

Compound heterozygote of cholesteryl-ester transfer protein deficiency in a patient with hyperalphalipoproteinemia.

H. Mabuchi, Akihiro Inazu, J. Koizumi, 1992, Atherosclerosis.

ApoVLDL of the Watanabe Heritable Hyperlipidemic rabbit and the cholesterol-fed rabbit.

Y. Watanabe, H. Mabuchi, J. Koizumi, 1984, Journal of lipid research.

Effects of ML-236b (compactin) on sterol synthesis and low density lipoprotein receptor activities in fibroblasts of patients with homozygous familial hypercholesterolemia.

H. Mabuchi, J. Koizumi, K. Ueda, 1981, The Journal of clinical investigation.

Serum and lipoprotein lipid levels in diabetic patients with familial hypercholesterolemia.

H. Mabuchi, J. Koizumi, T. Haba, 1983, The Tohoku journal of experimental medicine.

A case of heterozygous familial hypercholesterolemia associated with hyperthyroidism: effects of triiodothyronine on low-density lipoprotein receptor and cholesterol synthesis.

H. Mabuchi, J. Koizumi, S. Miyamoto, 1983, Metabolism: clinical and experimental.

A possible translational control of 3-hydroxy-3-methylglutaryl coenzyme A reductase induction by ML-236b(compactin) in isolated rat hepatocytes.

H. Mabuchi, J. Koizumi, R. Takeda, 1982, Biochemical and biophysical research communications.

Novel gene mutations at the low density lipoprotein receptor locus: FH‐Kanazawa and FH‐Okayama

H. Mabuchi, Akihiro Inazu, J. Koizumi, 1990, Journal of internal medicine.

Causes of death in patients with familial hypercholesterolemia.

H. Mabuchi, T. Wakasugi, K. Ueda, 1986, Atherosclerosis.

Serum apolipoproteins in heterozygous familial hypercholesterolemia.

H. Mabuchi, J. Koizumi, K. Kajinami, 1992, Clinica chimica acta; international journal of clinical chemistry.

A young type III hyperlipoproteinemic patient associated with apolipoprotein E deficiency.

H. Mabuchi, J. Koizumi, T. Wakasugi, 1989, Metabolism: clinical and experimental.

Enhanced Cholesteryl Ester Transfer Protein Activities and Abnormalities of High Density Lipoproteins in Familial Hypercholesterolemia

H. Mabuchi, Akihiro Inazu, J. Koizumi, 1992, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Lecithin: cholesterol acyl transfer rate in hypothyroidism and hyperthyroidism.

H. Mabuchi, J. Koizumi, S. Miyamoto, 1982, Endocrinologia japonica.

The incidence and pathogenesis of hyperlipidaemia in 16 consecutive acromegalic patients.

H. Mabuchi, K. Ueda, H. Nakabayashi, 1982, Acta endocrinologica.

Inhibition by somatostatin of insulin release from isolated pancreatic islets

H. Mabuchi, S. Miyamoto, R. Takeda, 1975, FEBS letters.

Effects of CS-514 (eptastatin), an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, on serum lipid and apolipoprotein levels in heterozygous familial hypercholesterolemic patients treated by low density lipoprotein (LDL)-apheresis.

H. Mabuchi, J. Koizumi, K. Kajinami, 1988, Atherosclerosis.

Mutations in the Low Density Lipoprotein Receptor Gene in Japanese Patients with Familial Hypercholesterolemia

H. Mabuchi, J. Koizumi, K. Kajinami, 1990, Annals of the New York Academy of Sciences.

Normalization of low-density lipoprotein levels and disappearance of xanthomas during pregnancy in a woman with heterozygous familial hypercholesterolemia.

H. Mabuchi, J. Koizumi, T. Haba, 1985, Metabolism: clinical and experimental.

Reduction of serum cholesterol in heterozygous patients with familial hypercholesterolemia. Additive effects of compactin and cholestyramine.

H. Mabuchi, J. Koizumi, H Mabuchi, 1983, The New England journal of medicine.

A new low density lipoprotein apheresis system using two dextran sulfate cellulose columns in an automated column regenerating unit (LDL continuous apheresis).

H. Mabuchi, J. Koizumi, I. Michishita, 1987, Atherosclerosis.

Serum lipids and coronary heart disease in heterozygous familial hypercholesterolemia in the Hokuriku District of Japan.

H. Mabuchi, J. Koizumi, K. Ueda, 1977, Atherosclerosis.

Serum lipids, lipoprotein lipids and coronary heart disease in patients with xanthelasma palpebrarum.

H. Mabuchi, J. Koizumi, K. Ueda, 1981, Atherosclerosis.

Achilles tendon thickness and ischemic heart disease in familial hypercholesterolemia.

H. Mabuchi, K. Ueda, S. Miyamoto, 1978, Metabolism: clinical and experimental.

Treatment of homozygous patients with familial hypercholesterolemia by double-filtration plasmapheresis.

H. Mabuchi, T. Wakasugi, I. Michishita, 1986, Atherosclerosis.

Homozygous familial hypercholesterolemia in Japan.

H. Mabuchi, J. Koizumi, K. Ueda, 1978, The American journal of medicine.

A massive pulmonary hemorrhage resulting in cavitation occurring in a case of hemophilia A associated with diabetes mellitus.

H. Mabuchi, R. Takeda, 1974, Southern medical journal.

Genetic cholesteryl ester transfer protein deficiency caused by two prevalent mutations as a major determinant of increased levels of high density lipoprotein cholesterol.

H. Mabuchi, Akihiro Inazu, J. Koizumi, 1994, The Journal of clinical investigation.