Mabuchi Hiroshi | Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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概要
- 同名の論文著者
- Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate Schoolの論文著者
関連著者
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Mabuchi Hiroshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Shimizu Masami
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Shimizu Masami
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Ino Hidekazu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Yamaguchi Masato
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Terai Hidenobu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Mizuno Sumio
福井心臓血圧センター
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Mizuno Sumio
金沢大学 循環器内科
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Sakata Kenji
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Kaneda Tomoya
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
著作論文
- PJ-424 Cardiac Sympathetic Nerve Activity in Patients with Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- Lispro is superior to regular insulin in transient intensive insulin therapy in type 2 diabetes
- Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy
- Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction
- PE-279 High Incidence of Sudden Cardiac Death with Conduction Disturbances and Atrial Cardiomyopathy Caused by a Mutation in the STA Gene(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- Reduction of hemolysis without reoperation following mitral valve repair
- Identification of two novel missense mutations (p.R1221C and p.R1357W) in the ABCC6 (MRP6) gene in a Japanese patient with pseudoxanthoma elasticum (PXE)
- Type III hyperlipoproteinemia exaggerated by Sheehan's syndrome with advanced systemic atherosclerosis - A 28-year clinical course
- Japan Lipid Intervention Trial (J-LIT) Chart Predicts the Absence of Coronary Artery Disease More Accurately Than Symptom Limited Exercise Stress Electrocardiography
- In-hospital Outcome in Octogenarians with Acute Coronary Syndrome Undergoing Emergent Coronary Angiography