Masuta Eiichi | Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science

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著作論文

Heterogeneity of Clinical Manifestation of Hypertrophic Cardiomyopathy Caused by Deletion of Lysine 183 in Cardiac Troponin I Gene : Insight From Two Autopsy Cases With an Identical Sarcomeric Gene Mutation
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)
PE-067 Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Hypertrophic Cardiomyopathy Caused by Cardiac Troponinl Gene Mutation(Cardiomyopathy, basic/clinical-3 (M) PE12,Poster Session (English),The 70th Anniversary Annual Scientific Meeting
OE-284 Usefulness of Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Patients with Hypertrophic Cardiomyopathy Associated with TNNI3 Gene Mutation(MRI/MRA-1 (I) OE48,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeti
FRS-077 Genetic Analysis of KCR1 Gene in Japanese LQTS Patients(Arrhythmia (basic), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
Gene mutations in adult Japanese patients with dilated cardiomyopathy
PJ-813 Impact of Speckle Tracking Echocardiography on Evaluation of Myocardial Fibrosis in Hypertrophic Cardiomyopathy : Comparison with Study by Cardiovascular Magnetic Resonance(PJ136,Echo/Doppler (Others) 1 (I),Poster Session (Japanese),The 73rd Annual
PJ-433 Impact of the HERG Channel Activator "Malltoxin" on Type 2 LQTS Related Mutant Channel(PJ073,Arrhythmia, Others (Basic) 1 (A),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
OE-022 Impact of Troponin-Gene Mutations on Occurrence of Atrial Fibrillation and Development of Left Atrial Dilatation in Hypertrophic Cardiomyopathy(OE04,Cardiomyopathy/Hypertrophy (Clinical) (M),Oral Presentation (English),The 73rd Annual Scientific Me
OE-019 Comparison of Phenotype of Hypertrophic Cardiomyopathy Associated with a Calcium Regulating Gene and a Sarcomere Gene(OE04,Cardiomyopathy/Hypertrophy (Clinical) (M),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circ
5 Impact of Combined Risk Factors on Reduction of Repolarization Reserve Associated with Drug-induced Abnormal QT Prolongation and Torsade de Pointes(Proarrhythmic Risk of Drugs and Their Evaluation,Symposium 7 (SY-07) (I),The 73rd Annual Scientific Meeti
PJ-632 Association between Atrial Fibrillation and Left Atrial Diameter in Genotyped Populations of Hypertrophic Cardiomyopathy : Results from a Longitudinal Study(Cardiomyopathy, basic / clinical(06)(M),Poster Session(Japanese),The 72nd Annual Scientific
PJ-202 Co-expression with Trafficking-competent KvLQT1 Selectively Rescues HERG LQT2 Mutations(Arrhythmia, basic(05)(A),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
PE-074 Impact of Left Ventricular Systolic Dysfunction on QT Dispersion and Associated Fatal Arrhythmia in Hypertrophic Cardiomyopathy(ECG/Body surface potential mapping/Holter(03)(A),Poster Session(English),The 72nd Annual Scientific Meeting of the Japan
OE-126 Angiotensin-Converting Enzyme D Allele is a Modifier Causing Left Ventricular Systolic Dysfunction in Genotyped Hypertrophic Cardiomyopathy : Results from Longitudinal Study(Heart failure, clinical(02)(M),Oral Presentation(English),The 72nd Annual
FRS-035 Impact of Elevated Matrix Metalloproteinase-2 on Prognosis in Hypertrophic Cardiomyopathy with Sarcomere Gene Mutations(Molecular Determinants for the Development of Cardiomyopathy(M),Featured Research Session,The 72nd Annual Scientific Meeting of
FRS-034 Impact of Anglotensin II Type 1 Receptor A/C1166 Gene Ploymorphism on the Onset of Atrial Fibrillation in Genotyped Hypertrophic Cardiomyopathy(Molecular Determinants for the Development of Cardiomyopathy(M),Featured Research Session,The 72nd Annu
2 Impact of Missense Mutations in Cardiac Ryanodine Receptor Gene as a Cause of Hypertrophic Cardiomyopathy : A New Insight From Ca Handling(Symposium 10 (SY-10) (M) Update in Cardiomyopathy : Novel Approaches ; Novel Targets,Special Program,The 72nd Annu
1 Prevalence of Long QT Syndrome and Frequencies of Gene Mutation Carriers in Japanese Children : an Epidemiological and Genetic Study(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Mee
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
PJ-085 Transient Improvement of Left Ventricular Diastolic Function After Low-density Lipoprotein Apheresis: Study with Tissue Doppler Imaging(Echo/Doppler(11)(I),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Soci
Occult aneurysms in aorto-coronary saphenous vein grafts
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)
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

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