Mabuchi Hiroshi | Division of Cardiology, Kanazawa University

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概要

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著作論文

Cardiac Sympathetic Nerve Activity and Left Ventricular Remodeling in Hypertrophic Cardiomyopathy(Cardiomyopathy, Clinical 3 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Regional Cardiac Sympathetic Nerve Function in Cardiomyopathies : Dilated Cardiomyopathy Versus Dilated Phase of Hypertrophic Cardiomyopathy(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Tissue Characteristics of Carotid Intima-media Complex Detected by Ultrasonic Integrated Backscatter (IBS) in Patients With Familial Hypercholesterolemia (FH)(Atherosclerosis, Clinical 4 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulatio
Diagnostic Usefullness of Achilles Tendon Thickness of Familial Hypercholesterolemia (FH) With Low-density-lipoprotein Receptor (LDLR) Gene Mutation(Lipid Disorders 2 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Enhanced Cholesterol Efflux from J774 Macrophages and Fu5AH Hepatoma Cells to Serum from CETP Deficiency(Atherosclerosis, Basic 6 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Synergistic Effects of Hepatic Lipase (HL) Promoter And CETP Promoter Polymorphism on Increased HDL-C Levels in Both Gender(Metabolism/Biochemistry/Energetics 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Cholesteryl Ester Transfer Protein (CETP) Promoter-1337 C/T Polymorphism Protect Against Coronary Atherosclerosis in Patient With Familial Hypercholesterolemia (FH)(Lipid Disorders 1 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Soci
Secreted Type II Phospholipase A_2 Decreases High-density-lipoprotein (HDL)-phospholipids and HDL_3-cholesterol in Human(Metabolism/Biochemistry/Energetics 1 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
RXRγ Gene Variant is Associated with Higher BMI, Lower HDL-C, Advanced Coronary Artery Disease, and Frequent in Familial Combined Hyperlipidemia(The Frontier of Atherosclerosis Research (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation
Distribution of QTc Values and Prevalence of Short QT Syndrome in the Japanese Population (ECG/Body Surface Potential Mapping/Holter 6 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Gene Mutations in Patients with Hypertrophic Cardiomyopathy Showing Mild Left Ventricular Hypertrophy(Cardiomyopathy, Clinical 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Differences in Diagnostic Value of Classic Electrocardiographic Voltage Criteria for Hypertrophic Cardiomyopathy in a Genotyped Population(Cardiomyopathy, Clinical 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Ankyrin-B Gene Mutation is a Rare Cause of Long QT Syndrome in Japan(Arrhythmia, Basic 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Long-Term Course of Patients with Cardiomyopathy Associated with Phospholamban Gene Mutations(Cardiomyopathy, Clinical 8 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Early Development of Dilated Cardiomyopathy in Subjects with Hypertrophic Cardiomyopathy Caused by Mutations of the Thin Filament Genes(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Angiotensin II Type 1 Receptor A/C1166 Gene Polymorphism and Left Ventricular Systolic Dysfunction in Hypertrophic Cardiomyopathy with Sarcomere Gene Mutations(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation
Impact of Bundle-Branch Block on Clinical Manifestation in Patients with Hypertrophic Cardiomyopathy : Analyses Based on Molecular Genetic Diagnoses(Cardiomyopathy, Clinical 6 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Cardiac Manifestations and Genotype-Phenotype Correlations in Carriers with the STA Gene Mutations(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Clinical Features of Hypertrophic Cardiomyopathy Caused by a Novel Val85Leu Missense Mutation in the Cardiac Troponin T Gene(Cardiomyopathy, Clinical 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
The Relationship of Percent Body Fat by Bioelectrical Impedance Analysis with Blood Pressure, and Glucose and Lipid Parameters
Prevalence and Onset of Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 6 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Can LQT1 be Differentiated with ST-T Morphology from the Other Type of Long QT Syndrome?(Arrhythmia, Diagnosis/Pathophysiology/EPS 6 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Prevalence of Gene Mutations in Patients with Congenital Long QT Syndrome(Arrhythmia, Basic 2 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Prevalence of Long QT Syndrome in Japanese Children(ECG/Body Surface Potential Mapping/Holter 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)

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