Ino Hidekazu | Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medicine

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著作論文

Impact of Severe Earthquake on the Occurrence of Acute Coronary Syndrome and Stroke in a Rural Area of Japan : Experience From the Noto Peninsula Earthquake
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)
Marked Aortic Valve Stenosis Progression After Receiving Long-Term Aggressive Cholesterol-Lowering Therapy Using Low-Density Lipoprotein Apheresis in a Patient With Familial Hypercholesterolemia
4 Morphology and Histological Assessment of Vulnerable Plaque Accompanying No-reflow Phenomenon after Intervention in Acute Coronary Syndrome(Symposium 13 (SY-13) (I) Freshscent Forefront in Atherosclerotic Plaque Imagings,Special Program,The 72nd Annual
PJ-341 Intravascular Ultrasound Virtual Histology Images and Pathological Analysis of Materials Captured by Filter Device in Patients With Acute Coronary Syndrome(Intravascular endoscopy/Intravascular ultrasound(06)(I),Poster Session(Japanese),The 72nd An
4 Morphologic Impacts of Angiography and Intravascular Ultrasound on Predicting Prognosis of Acute Coronary Syndrome : Unresolved Issue of No-reflow Phenomenon(New Risk Stratification for Cardiac Events after Acute Myocardial Infarction,Topic 1 (TP-1) (IH
FRS-077 Genetic Analysis of KCR1 Gene in Japanese LQTS Patients(Arrhythmia (basic), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
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
OE-007 Transient Overexpression of Heme Oxygenase-1 Promotes Cardioprotection in Ischemic Myocardial Injury through Antioxidative Stress and -apoptotic Activities(OE02,ACS/AMI (Basic) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of
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-564 Transient Overexpression of Heme Oxygenage-1 Promotes Tolerance of Transplanted Mesenchymal Stem Cells to Oxidative Stress(Regeneration (angiogenesis/myocardial regeneration)(05)(M),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the
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-493 Impact of Insulin Resistance on Coronary Ectasia : Results from Study on Heterozygous Familial Hypercholesterolemia with Common LDL Receptor Mutation(Diabetes/Obesity/Metabolic syndrome-08, The 71st Annual Scientific Meeting of the Japanese Circula
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-274 A New Device for Transluminal Removal of Expanded Vascular Stent : an in Vivo Feasibility Study(PJ046,Coronary Revascularization, PCI (New Devices/New Technology) 2 (IHD),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese
PE-037 Analysis of the Causes for Delay in Emergency Call in Japanese Cardiac Arrests : Need of Public Relations for Early Call(PE007,Preventive Medicine/Epidemiology/Education 1 (H),Poster Session (English),The 73rd Annual Scientific Meeting of The Japan
PJ-656 A New Device for Transluminal Removal of Coronary Stent(Coronary revascularization, PCI(24)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
PJ-366 Delayed Occurrence of Cerebrovascular Events After Severe Earthquake in Japan : Comparison With Cardiovascular Events(Preventive medicine/Epidemiology/Education(06)(H),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circ
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
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
PJ-443 Impact of Primary Aldosteronism on Occurrence of Atrial Fibrillation and Cerebral Events(PJ075,Hypertension, Clinical 1 (H),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
Impact of Renin-Angiotensin System Polymorphisms on Development of Systolic Dysfunction in Hypertrophic Cardiomyopathy : Evidence From a Study of Genotyped Patients
Unusual biatrial thrombus in mitral stenosis

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