Inazu A - Search Results

1

Effects of serum B vitamins on elevated plasma homocysteine levels associated with the mutation of methylenetetrahydrofolate reductase gene in Japanese.

Moriyama Y, Okamura T, Kajinami K, Iso H, Inazu A, Kawashiri M, Mizuno M, Takeda Y, Sakamoto Y, Kimura H, Suzuki H, Mabuchi H. Moriyama Y, et al. Among authors: inazu a. Atherosclerosis. 2002 Oct;164(2):321-8. doi: 10.1016/s0021-9150(02)00105-3. Atherosclerosis. 2002. PMID: 12204804

2

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

Takegoshi T, Haba T, Kitoh C, Inazu A, Koizumi J, Mabuchi H, Takeda R. Takegoshi T, et al. Among authors: inazu a. Atherosclerosis. 1992 Sep;96(1):83-5. doi: 10.1016/0021-9150(92)90040-n. Atherosclerosis. 1992. PMID: 1418105 No abstract available.

3

Enhanced cholesteryl ester transfer protein activities and abnormalities of high density lipoproteins in familial hypercholesterolemia.

Inazu A, Koizumi J, Mabuchi H, Kajinami K, Takeda R. Inazu A, et al. Horm Metab Res. 1992 Jun;24(6):284-8. doi: 10.1055/s-2007-1003314. Horm Metab Res. 1992. PMID: 1634194

4

Serum lipoprotein lipid concentration and composition in homozygous and heterozygous patients with cholesteryl ester transfer protein deficiency.

Koizumi J, Inazu A, Yagi K, Koizumi I, Uno Y, Kajinami K, Miyamoto S, Moulin P, Tall AR, Mabuchi H, et al. Koizumi J, et al. Among authors: inazu a. Atherosclerosis. 1991 Oct;90(2-3):189-96. doi: 10.1016/0021-9150(91)90114-i. Atherosclerosis. 1991. PMID: 1759989

5

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

Kajinami K, Mabuchi H, Inazu A, Fujita H, Koizumi J, Takeda R, Matsue T, Kibata M. Kajinami K, et al. Among authors: inazu a. J Intern Med. 1990 Apr;227(4):247-51. doi: 10.1111/j.1365-2796.1990.tb00153.x. J Intern Med. 1990. PMID: 2324680

6

Effects on coronary atherosclerosis of long-term treatment of familial hypercholesterolemia by LDL-apheresis.

Mabuchi H, Koizumi J, Michishita I, Takeda M, Kajinami K, Fujita H, Inazu A, Uno Y, Shimizu M, Takeda R, et al. Mabuchi H, et al. Among authors: inazu a. Beitr Infusionsther. 1988;23:87-96. Beitr Infusionsther. 1988. PMID: 2484787 No abstract available.

7

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

Koizumi J, Inazu A, Fujita H, Takeda M, Uno Y, Kajinami K, Mabuchi H, Takeda R. Koizumi J, et al. Among authors: inazu a. Atherosclerosis. 1988 Nov;74(1-2):1-8. doi: 10.1016/0021-9150(88)90184-0. Atherosclerosis. 1988. PMID: 3145747

8

Molecular genetics of cholesterol transport and cholesterol reverse transport disorders (familial hypercholesterolemia and CETP deficiency) and coronary heart disease.

Mabuchi H, Yagi K, Haraki T, Matsushita H, Inazu A, Kajinami K, Koizumi J. Mabuchi H, et al. Among authors: inazu a. Ann N Y Acad Sci. 1995 Jan 17;748:333-41. doi: 10.1111/j.1749-6632.1994.tb17330.x. Ann N Y Acad Sci. 1995. PMID: 7695176 No abstract available.

9

Absence of familial defective apolipoprotein B-100 in Japanese patients with familial hypercholesterolaemia.

Nohara A, Yagi K, Inazu A, Kajinami K, Koizumi J, Mabuchi H. Nohara A, et al. Among authors: inazu a. Lancet. 1995 Jun 3;345(8962):1438. doi: 10.1016/s0140-6736(95)92627-5. Lancet. 1995. PMID: 7760626 No abstract available.

10

[CETP deficiency].

Inazu A, Koizumi J, Mabuchi H. Inazu A, et al. Nihon Rinsho. 1994 Dec;52(12):3216-20. Nihon Rinsho. 1994. PMID: 7853713 Review. Japanese.

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