Yagi K - Search Results

1

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

Mabuchi H, Nohara A, Noguchi T, Kobayashi J, Kawashiri MA, Inoue T, Mori M, Tada H, Nakanishi C, Yagi K, Yamagishi M, Ueda K, Takegoshi T, Miyamoto S, Inazu A, Koizumi J; Hokuriku FH Study Group. Mabuchi H, et al. Among authors: yagi k. Atherosclerosis. 2014 Sep;236(1):54-61. doi: 10.1016/j.atherosclerosis.2014.06.005. Epub 2014 Jun 26. Atherosclerosis. 2014. PMID: 25014035

2

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: yagi k. Atherosclerosis. 1991 Oct;90(2-3):189-96. doi: 10.1016/0021-9150(91)90114-i. Atherosclerosis. 1991. PMID: 1759989

3

Clinical efficacy of fluvastatin in the long-term treatment of familial hypercholesterolemia.

Koizumi J, Haraki T, Yagi K, Inazu A, Kajinami K, Miyamoto S, Ueda K, Ohta M, Takegoshi T, Takeda M, et al. Koizumi J, et al. Among authors: yagi k. Am J Cardiol. 1995 Jul 13;76(2):47A-50A. doi: 10.1016/s0002-9149(05)80016-5. Am J Cardiol. 1995. PMID: 7604797 Clinical Trial.

4

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: yagi k. 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.

5

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: yagi k. Lancet. 1995 Jun 3;345(8962):1438. doi: 10.1016/s0140-6736(95)92627-5. Lancet. 1995. PMID: 7760626 No abstract available.

6

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

Inazu A, Jiang XC, Haraki T, Yagi K, Kamon N, Koizumi J, Mabuchi H, Takeda R, Takata K, Moriyama Y, et al. Inazu A, et al. Among authors: yagi k. J Clin Invest. 1994 Nov;94(5):1872-82. doi: 10.1172/JCI117537. J Clin Invest. 1994. PMID: 7962532 Free PMC article.

7

Reduction of lipoprotein(a) by LDL-apheresis using a dextran sulfate cellulose column in patients with familial hypercholesterolemia.

Koizumi J, Koizumi I, Uno Y, Inazu A, Kajinami K, Haraki T, Yagi K, Kamon N, Miyamoto S, Takegoshi T, et al. Koizumi J, et al. Among authors: yagi k. Atherosclerosis. 1993 Apr;100(1):65-74. doi: 10.1016/0021-9150(93)90068-6. Atherosclerosis. 1993. PMID: 8318064

8

Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by an intron 14 splicing defect in hyperalphalipoproteinemia.

Inazu A, Koizumi J, Haraki T, Yagi K, Wakasugi T, Takegoshi T, Mabuchi H, Takeda R. Inazu A, et al. Among authors: yagi k. Hum Genet. 1993 Mar;91(1):13-6. doi: 10.1007/BF00230214. Hum Genet. 1993. PMID: 8454281

9

Clinical characteristics of double heterozygotes with familial hypercholesterolemia and cholesteryl ester transfer protein deficiency.

Haraki T, Inazu A, Yagi K, Kajinami K, Koizumi J, Mabuchi H. Haraki T, et al. Among authors: yagi k. Atherosclerosis. 1997 Jul 25;132(2):229-36. doi: 10.1016/s0021-9150(97)00093-2. Atherosclerosis. 1997. PMID: 9242969

10

Low-density lipoprotein receptor genotype-dependent response to cholesterol lowering by combined pravastatin and cholestyramine in familial hypercholesterolemia.

Kajinami K, Yagi K, Higashikata T, Inazu A, Koizumi J, Mabuchi H. Kajinami K, et al. Among authors: yagi k. Am J Cardiol. 1998 Jul 1;82(1):113-7. doi: 10.1016/s0002-9149(98)00230-6. Am J Cardiol. 1998. PMID: 9671018

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