K. Ueda

发表

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

M. Yamagishi, H. Mabuchi, J. Kobayashi, 2014, Atherosclerosis.

Spontaneous development of left ventricular aneurysm in a patient with untreated cardiac sarcoidosis.

J. Taki, H. Mabuchi, T. Haraki, 2002, Circulation journal : official journal of the Japanese Circulation Society.

Sheehan's syndrome with hypomagnesemia and polymorphous ventricular tachycardia.

S. Nunoda, H. Nakabayashi, S. Kameda, 1989, Japanese heart journal.

Risk evaluation of coronary heart disease and cerebrovascular disease by the Japan Atherosclerosis Society Guidelines 2002 using the cohort of the Holicos-PAT study.

M. Ohta, H. Mabuchi, J. Koizumi, 2005, Journal of atherosclerosis and thrombosis.