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H Rakugi

Showing results (61-70 of 95) with videos related to

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Journal of Human Hypertension|April 24, 2001
A common mutation of low-density lipoprotein receptor gene is associated with essential hypertension among JapaneseY Fu, T Katsuya, J Higaki, et al.
American Journal of Hypertension|April 17, 1998
Angiotensin II type 1 receptor gene polymorphism is associated with increase of left ventricular mass but not with hypertensionS Takami, T Katsuya, H Rakugi, et al.
Hypertension (Dallas, Tex. : 1979)|February 4, 1999
Angiotensin II type 1 receptor-mediated peroxide production in human macrophagesY Yanagitani, H Rakugi, A Okamura, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|August 1, 1986
[A case with non-Hodgkin lymphoma manifesting chylothorax and chylous ascites]H Rakugi, T Ogihara, H Mikami, et al.
Journal of Hypertension|July 15, 1999
Upregulation of renin-angiotensin system during differentiation of monocytes to macrophagesA Okamura, H Rakugi, M Ohishi, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|June 1, 1986
[An autopsied case of a 45-year-old man with Hutchinson-Gilford progeria syndrome]T Ogihara, Y Tabuchi, K C Fukuchi, et al.
American Journal of Hypertension|January 1, 1997
Trp64Arg mutation of beta3-adrenergic receptor in essential hypertension: insulin resistance and the adrenergic systemT Fujisawa, H Ikegami, E Yamato, et al.
American Journal of Hypertension|January 27, 1998
Polymorphism of angiotensin converting enzyme, angiotensinogen, and apolipoprotein E genes in a Japanese population with cerebrovascular diseaseY Nakata, T Katsuya, H Rakugi, et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|June 1, 1996
Analysis of candidate genes for insulin resistance in essential hypertensionH Ikegami, E Yamato, T Fujisawa, et al.
Nihon Naibunpi Gakkai Zasshi|February 20, 1990
[A case of recessive dystrophic epidermolysis bullosa associated with dwarfism with special reference to pathophysiological role of growth hormone]F Nakamura, H Rakugi, K Fukuo, et al.
Pageof 10

Showing results (61-70 of 95) with videos related to

Sort By:
Pageof 10
Journal of Human Hypertension|April 24, 2001
A common mutation of low-density lipoprotein receptor gene is associated with essential hypertension among JapaneseY Fu, T Katsuya, J Higaki, et al.
American Journal of Hypertension|April 17, 1998
Angiotensin II type 1 receptor gene polymorphism is associated with increase of left ventricular mass but not with hypertensionS Takami, T Katsuya, H Rakugi, et al.
Hypertension (Dallas, Tex. : 1979)|February 4, 1999
Angiotensin II type 1 receptor-mediated peroxide production in human macrophagesY Yanagitani, H Rakugi, A Okamura, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|August 1, 1986
[A case with non-Hodgkin lymphoma manifesting chylothorax and chylous ascites]H Rakugi, T Ogihara, H Mikami, et al.
Journal of Hypertension|July 15, 1999
Upregulation of renin-angiotensin system during differentiation of monocytes to macrophagesA Okamura, H Rakugi, M Ohishi, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|June 1, 1986
[An autopsied case of a 45-year-old man with Hutchinson-Gilford progeria syndrome]T Ogihara, Y Tabuchi, K C Fukuchi, et al.
American Journal of Hypertension|January 1, 1997
Trp64Arg mutation of beta3-adrenergic receptor in essential hypertension: insulin resistance and the adrenergic systemT Fujisawa, H Ikegami, E Yamato, et al.
American Journal of Hypertension|January 27, 1998
Polymorphism of angiotensin converting enzyme, angiotensinogen, and apolipoprotein E genes in a Japanese population with cerebrovascular diseaseY Nakata, T Katsuya, H Rakugi, et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|June 1, 1996
Analysis of candidate genes for insulin resistance in essential hypertensionH Ikegami, E Yamato, T Fujisawa, et al.
Nihon Naibunpi Gakkai Zasshi|February 20, 1990
[A case of recessive dystrophic epidermolysis bullosa associated with dwarfism with special reference to pathophysiological role of growth hormone]F Nakamura, H Rakugi, K Fukuo, et al.
Pageof 10