Hayashi Kenshi | Division Of Cardiology Ishikawa Prefectural Hospital

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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
OE-265 Genotype-Phenotype Variations in Cardiomyopathies Caused by a Cardiac Troponin I Gene Mutation(Cardiomyopathy, basic/clinical-1 (M) OE45,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
OE-088 Differences in Diagnostic Value of Various Criteria of Negative T Waves for Hypertrophic Cardiomyopathy in a Genotyped Population(ECG/Body surface potential mapping/Holter-1 (A) OE15,Oral Presentation (English),The 70th Anniversary Annual Scientifi
FRS-077 Genetic Analysis of KCR1 Gene in Japanese LQTS Patients(Arrhythmia (basic), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
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)
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
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)
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
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)
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-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)
1P-318 DNAナノ構造体の作製法の確立(バイオエンジニアリング,第46回日本生物物理学会年会)
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)
Multiplexed Analysis of Post-PCR Fluorscence-labeled Microsatellite Alleles and Statistical Evaluation of Their Imbalance in Brain Tumors
Characterization of the Biological Functions of a Transcription Factor, c-myc Intron Binding Protein 1 (MIBP1)^1
2P336 自己集合核酸によるアドレス可能な内破的ナノ構造体(バイオエンジニアリング,第48回日本生物物理学会年会)
2P-275 自己集合核酸からなる拡張可能なナノトラス構造体 : そのデザインと階層的な構築(バイオエンジニアリング,第47回日本生物物理学会年会)
Prolonged Atrioventricular Block and Ventricular Standstill Following Adenosine Triphosphate Injection in a Patient Taking Dipyridamole and Antiarrhythmic Agents : A Case Report
Impact of Renin-Angiotensin System Polymorphisms on Development of Systolic Dysfunction in Hypertrophic Cardiomyopathy : Evidence From a Study of Genotyped Patients
Impact of reduced left atrial functions on diagnosis of paroxysmal atrial fibrillation : Results from analysis of time-left atrial volume curve determined by two-dimensional speckle tracking
Gene and Protein Expression Analysis of Mesenchymal Stem Cells Derived From Rat Adipose Tissue and Bone Marrow
Impact of the right parasternal view with supine positioning for echocardiographic visualization of acute type A aortic dissection
Cardiac papillary fibroelastoma originated from atrial side of mitral valve leaflet
Impact of Gain-of-Function Gene Variant of SCN1B T189M, on Occurrence of Lone Atrial Fibrillation
Non-bacterial thrombotic endocarditis associated with Trousseau's syndrome
Characterization of the Biological Functions of a Transcription Factor, c-myc Intron Binding Protein 1 (MIBP1).
Transient expression of cellular retinol-binding protein-1 during cardiac repair after myocardial infarction

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