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S Tsutaya

Showing results (1-10 of 10) with videos related to

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Rinsho Byori. the Japanese Journal of Clinical Pathology|January 23, 1999
[Endothelial nitric oxide synthase gene polymorphism and hypertension]M Yasujima, S Tsutaya, M Shoji
Rinsho Byori. the Japanese Journal of Clinical Pathology|April 20, 2001
[Hypertension and gene polymorphisms]M Shoji, S Tsutaya, H Takamatu, et al.
Life Sciences|July 7, 2000
Positive association of endothelial nitric oxide synthase gene polymorphism with hypertension in northern JapanM Shoji, S Tsutaya, R Saito, et al.
The Tohoku Journal of Experimental Medicine|June 1, 1997
Angiotensin converting enzyme gene polymorphism and its enzyme activity in serum in young Japanese femalesS Tsutaya, H Kitaya, Y Saito, et al.
The Tohoku Journal of Experimental Medicine|September 30, 1999
Analysis of aldehyde dehydrogenase 2 gene polymorphism and ethanol patch test as a screening method for alcohol sensitivityS Tsutaya, M Shoji, Y Saito, et al.
Clinical Nephrology|January 25, 2006
A novel mutation of the thiazide-sensitive sodium chloride cotransporter gene in a Japanese family with Gitelman syndromeK Terui, M Shoji, J Yamashiki, et al.
Journal of Human Hypertension|July 27, 2007
Association of novel promoter single nucleotide polymorphisms in vasopressin V1a receptor gene with essential hypertension in nonobese JapaneseK N Hasan, M Shoji, K Sugimoto, et al.
Journal of Endocrinological Investigation|December 24, 2005
Diagnosis of a case of Gitelman's syndrome based on renal clearance studies and gene analysis of a novel mutation of the thiazide-sensitive Na-Cl cotransporterK Kageyama, K Terui, M Shoji, et al.
Journal of Endocrinological Investigation|February 6, 2008
A case of thyrotropin-producing pituitary adenoma, accompanied by an increase in anti-thyrotropin receptor antibody after tumor resectionK Kageyama, H Ikeda, S Sakihara, et al.
Journal of Endocrinological Investigation|December 23, 2006
Gene analysis of the calcium channel 1 subunit and clinical studies for two patients with hypokalemic periodic paralysisK Kageyama, K Terui, S Tsutaya, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Rinsho Byori. the Japanese Journal of Clinical Pathology|January 23, 1999
[Endothelial nitric oxide synthase gene polymorphism and hypertension]M Yasujima, S Tsutaya, M Shoji
Rinsho Byori. the Japanese Journal of Clinical Pathology|April 20, 2001
[Hypertension and gene polymorphisms]M Shoji, S Tsutaya, H Takamatu, et al.
Life Sciences|July 7, 2000
Positive association of endothelial nitric oxide synthase gene polymorphism with hypertension in northern JapanM Shoji, S Tsutaya, R Saito, et al.
The Tohoku Journal of Experimental Medicine|June 1, 1997
Angiotensin converting enzyme gene polymorphism and its enzyme activity in serum in young Japanese femalesS Tsutaya, H Kitaya, Y Saito, et al.
The Tohoku Journal of Experimental Medicine|September 30, 1999
Analysis of aldehyde dehydrogenase 2 gene polymorphism and ethanol patch test as a screening method for alcohol sensitivityS Tsutaya, M Shoji, Y Saito, et al.
Clinical Nephrology|January 25, 2006
A novel mutation of the thiazide-sensitive sodium chloride cotransporter gene in a Japanese family with Gitelman syndromeK Terui, M Shoji, J Yamashiki, et al.
Journal of Human Hypertension|July 27, 2007
Association of novel promoter single nucleotide polymorphisms in vasopressin V1a receptor gene with essential hypertension in nonobese JapaneseK N Hasan, M Shoji, K Sugimoto, et al.
Journal of Endocrinological Investigation|December 24, 2005
Diagnosis of a case of Gitelman's syndrome based on renal clearance studies and gene analysis of a novel mutation of the thiazide-sensitive Na-Cl cotransporterK Kageyama, K Terui, M Shoji, et al.
Journal of Endocrinological Investigation|February 6, 2008
A case of thyrotropin-producing pituitary adenoma, accompanied by an increase in anti-thyrotropin receptor antibody after tumor resectionK Kageyama, H Ikeda, S Sakihara, et al.
Journal of Endocrinological Investigation|December 23, 2006
Gene analysis of the calcium channel 1 subunit and clinical studies for two patients with hypokalemic periodic paralysisK Kageyama, K Terui, S Tsutaya, et al.
Pageof 1