E. Takeshita

发表

Insulin resistance syndrome in adolescents and adults.

T. Saruta, I. Saito, H. Kawabe, 1996, Hypertension research : official journal of the Japanese Society of Hypertension.

Association between platelet glycoprotein Ibalpha genotype and ischemic cerebrovascular disease.

Masahiro Yamamoto, Y. Fukuuchi, D. Ito, 2000, Stroke.

Excretion and metabolism of dopa and dopamine by isolated perfused rat kidney.

T. Saruta, H. Suzuki, M. Kawamura, 1984, The American journal of physiology.

EFFECT OF A CALCIUM ENTRY BLOCKER ON BLOOD PRESSURE, PLASMA RENIN ACTIVITY, ALDOSTERONE AND CATECHOLAMINES IN NORMOTENSIVE SUBJECTS

T. Saruta, I. Saito, S. Nagano, 1986, Clinical endocrinology.

Effect of L-dopa in Young Patients with Hypertension

T. Saruta, I. Saito, H. Yamakawa, 1991, Angiology.

Blood Pressure Response to a Calcium Entry Blocker in Normotensive Subjects With or Without a Family History of Hypertension

T. Saruta, I. Saito, S. Nagano, 1987, Angiology.

Increased urinary dopamine excretion in young patients with essential hypertension.

T. Saruta, I. Saito, H. Kawabe, 1994, Clinical and experimental hypertension.

Urinary dopamine excretion in normotensive subjects with or without family history of hypertension.

T. Saruta, I. Saito, S. Nagano, 1986, Journal of hypertension.

Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates.

Takao Takahashi, T. Ohashi, T. Hasegawa, 2004, The Journal of clinical endocrinology and metabolism.

Current status of surviving patients with arginase 1 deficiency in Japan

J. Kagawa, F. Endo, Keitaro Yamada, 2021, Molecular genetics and metabolism reports.

Reference values for urinary steroids in Japanese newborn infants: gas chromatography/mass spectrometry in selected ion monitoring.

Takao Takahashi, H. Chiba, T. Hasegawa, 2003, Endocrine journal.

Evidence for Abnormalities in Parasympathetic Nerve-Mediated Reflexes in Borderline Hypertension

T. Saruta, Y. Kanno, H. Nakamoto, 1993 .

Cholesteryl ester transfer protein polymorphism associated with macroangiopathy in Japanese patients with type 2 diabetes.

T. Saruta, K. Watanabe, I. Takei, 2001, Atherosclerosis.

Effect of Captopril on Plasma Prolactin in Patients with Essential Hypertension

T. Saruta, S. Hayashi, I. Saito, 1990, Angiology.

Comparison of clinic and home blood pressure levels and the role of the sympathetic nervous system in clinic-home differences.

T. Saruta, I. Saito, T. Takenaka, 1990, American journal of hypertension.

Angiotensin converting enzyme insertion/deletion polymorphism is associated with plasma antigen levels of plasminogen activator inhibitor-1 in healthy Japanese population.

M. Murata, Y. Ikeda, Y. Matsubara, 2000, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

[Genetic risk factors for ischemic cerebrovascular disease--analysis on fifteen candidate prothrombotic gene polymorphisms in the Japanese population].

Y. Fukuuchi, D. Ito, M. Murata, 2004, Rinsho byori. The Japanese journal of clinical pathology.

Factor XII Shizuoka, a novel mutation (Ala392Thr) identified and characterized in a patient with congenital coagulation factor XII deficiency.

M. Murata, Y. Ikeda, Kiyoaki Watanabe, 2005, Thrombosis research.

Activated factor XII levels are dependent on factor XII 46C/T genotypes and factor XII zymogen levels, and are associated with vascular risk factors in patients and healthy subjects.

K. Matsumoto, D. Ito, M. Kitajima, 2000, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Genetic analyses and expression studies identified a novel mutation (W486C) as a molecular basis of congenital coagulation factor XII deficiency

M. Murata, Y. Ikeda, Kiyoaki Watanabe, 2004, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.