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Japanese Circulation Journal|June 16, 2001
Arrhythmias in patients with Brugada-type electrocardiographic findingsH Itoh, M Shimizu, H Ino, et al.Hypertension (Dallas, Tex. : 1979)|October 23, 1997
Brain nitric oxide synthase messenger RNA in central mineralocorticoid hypertensionY Takeda, I Miyamori, T Yoneda, et al.Endokrinologie|February 1, 1982
Secondary type V hyperlipoproteinemia in an acromegalic patient without overt diabetesR Takeda, R Tatami, K Ueda, et al.Atherosclerosis|July 1, 1986
Causes of death in patients with familial hypercholesterolemiaH Mabuchi, S Miyamoto, K Ueda, 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.Clinical Endocrinology|June 26, 2001
Genetic analysis of the cytochrome P-450c17alpha (CYP17) and aldosterone synthase (CYP11B2) in Japanese patients with 17alpha-hydroxylase deficiencyY Takeda, T Yoneda, M Demura, et al.Journal of Cardiovascular Pharmacology|January 1, 1995
Effect of FK 506 on the expression of endothelin receptor mRNA in the vasculatureY Takeda, I Miyamori, P Wu, et al.Atherosclerosis|January 1, 1986
Coronary ectasia in a homozygous patient with familial hypercholesterolemiaH Mabuchi, I Michishita, Y Sakai, et al.Atherosclerosis|August 1, 1986
Treatment of homozygous patients with familial hypercholesterolemia by double-filtration plasmapheresisH Mabuchi, I Michishita, T Sakai, et al.American Journal of Hematology|September 1, 1996
Absence of CD69 expression on peripheral eosinophils in episodic angioedema and eosinophiliaM Kawano, H Muramoto, S Tsunoda, et al.Pageof 21