Katoh Hiromasa | Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medicine

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著作論文

OE-084 Impact of Gene Mutation Regions of HERG Channel, Pore or Nonpore, on Clinical Course of LQTS(Arrhythmia, basic-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
FRS-077 Genetic Analysis of KCR1 Gene in Japanese LQTS Patients(Arrhythmia (basic), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PJ-524 Extent and Localization of Myocardial Fibrosis in Hypertrophic Cardiomyopathy Associated with Sarcomere Protein Gene Mutation : Study by Magnetic Resonance Imaging(MRI/MRA-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PE-558 Prevalence of Long QT Syndrome and Frequencies of Gene Mutation Carriers in Japanese Children(Preventive medicine/Epidemiology/Education-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PE-437 Progressive LV Remodeling and Adverse Cardiac Events in HCM Associated With Mutations in Cardiac Troponin Genes : Longitudinal 10 years Follow-up(Heart failure, basic-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
OJ-240 Dilated-Phase Hypertrophic Cardiomyopathy Show More Severe Heart Failure Compared with Idiopathic Dilated Cardiomyopathy in Matched Symptomatic and Echocardiographic Settings(Heart failure, clinical-06, The 71st Annual Scientific Meeting of the Jap
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)
Mutation of the β Myosin Heavy Chain Gene associated with Isolated Left Ventricular Noncompaction(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
OJ-051 Elevation of Plasma Levels of Matrix Metalloproteinase-2 Involves Development of Myocardial Fibrosis in HCM Caused by TNNI3 Gene Mutations(Cardiomyopathy, basic/clinical-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
OE-296 Unusual Left Atrial Dilation in Genotyped Hypertrophic Cardiomyopathy : Evidence from 10 Years Follow-up of the Cardiac Troponin I Mutation Carriers(Cardiomyopathy, basic/clinical-1, The 71st Annual Scientific Meeting of the Japanese Circulation So
OE-294 Differences in Diagnostic Value of Abnormal Q Waves for Detecting Carriers of Hypertrophic Cardiomyopathy with Thin and Thick Filament-Gene Mutations(Cardiomyopathy, basic/clinical-1, The 71st Annual Scientific Meeting of the Japanese Circulation S
OE-293 Clinical and Genetic Determinants of Atrial Fibrillation in Genotyped Populations of Hypertrophic Cardiomyopathy(Cardiomyopathy, basic/clinical-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
OE-292 Development of Left Ventricular Hypertrophy and Remodeling in Hypertrophic Cardiomyopathy Caused by a TNNI3 Gene Mutation : a Longitudinal Study(Cardiomyopathy, basic/clinical-1, The 71st Annual Scientific Meeting of the Japanese Circulation Societ
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)

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