OJ-511 Missense Mutations in Cardiac Ryanodine Receptor Gene Cause Hypertrophic Cardiomyopathy Associated with Ventricular Arrhythmia or Massive Hypertrophy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
スポンサーリンク
概要
- 論文の詳細を見る
- 社団法人日本循環器学会の論文
- 2004-03-01
著者
-
Terai Hidenobu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Ino Hidekazu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Fujino Noboru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Shimizu Masami
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Terai Hidenobu
Division of Cardiology, Kanazawa Cardiovascular Hospital
-
Yamaguchi Masato
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Sakata Kenji
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Inoue Masaru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Mabuchi Hiroshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Shimizu Masami
Cardiovascular Checkup Committee For School Pupils Of Kanazawa Medical Association
-
Mizuno Sumio
福井心臓血圧センター
-
Mizuno Sumio
金沢大学 循環器内科
-
Terai Hidenobu
Division Of Cardiology Kanazawa Cardiovascular Hospital
-
Inoue Masaru
Division Of Cardiology Ishikawa Prefectural Hospital
-
Sakata Kenji
金沢大学 医学系研究科循環器内科学
-
Kaneda Tomoya
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Kaneda Tomoya
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Inoue Masaru
Department Of Cardiology Ishikawa Prefectural Central Hospital
-
Shimizu Masami
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Seidman Christine
Harvard Medical School
-
Seidman Christine
Department Of Genetics Harvard Medical School
-
Seidman Jonathan
Harvard Medical School
-
Terai Hidenobu
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Seidman Jonathan
Department Of Genetics Harvard Medical School
-
Sakata Kenji
Department Of Cardiology Ishikawa Prefectural Central Hospital
-
Kametani Tomio
Department Of Internal Medicine Koseiren Takaoka Hospital
-
Itoh Hideki
Department Of Emergency And Critical Care Medicine Kanazawa University Hospital
-
Inaba Hideo
Department Of Emergency And Critical Care Medicine Kanazawa University Hospital
-
Mabuchi Hiroshi
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Yamaguchi Masato
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
関連論文
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- 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
- OJ-223 A Novel Missense Mutation Met1107Thr in Cardiac Ryanodine Receptor Gene is Associated with Hypertrophic Cardiomyopathy(Cardiomyopathy, basic/clinical-2 (M) OJ38,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japa
- 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-104 Association between Angiotensin II Receptor Gene Polymorphism and Left Ventricular Systolic Dysfunction in Sarcomere Gene Mutation-induced Hypertrophic Cardiomyopathy(Frontier of Cardiomyopathy Research-2 (M) FRS21,Featured Research Session (Engli
- 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)
- PJ-424 Cardiac Sympathetic Nerve Activity in Patients with Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- FRS-149 Mutation Site-Specific Differences in Arrhythmic Risk and Sensitivity to Sympathetic Stimulation in Japanese Families with Congenital LQT1 Syndrome(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- 5 Genotype- and Mutation site-Specific Differences in Arrhythmic Risk and Sensitivity to Sympathetic Stimulation in the Long QT Syndrome(APSC/JCS Joint Symposium (APSC) (H) : Emerging Issue in Cardiology for Asian)(Special Program)
- Three Cases of Iatrogenic Coronary Ostial Stenosis After Aortic Valve Replacement
- Lispro is superior to regular insulin in transient intensive insulin therapy in type 2 diabetes
- Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy
- Risk Evaluation of Coronary Heart Disease and Cerebrovascular Disease by the Japan Atherosclerosis Society Guidelines 2002 Using the Cohort of the Holicos-PAT Study
- Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction
- PE-279 High Incidence of Sudden Cardiac Death with Conduction Disturbances and Atrial Cardiomyopathy Caused by a Mutation in the STA Gene(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- Reduction of hemolysis without reoperation following mitral valve repair
- PE-237 Cholesterol-years Score is Associated with Development of Senile Degenerative Aortic Stenosis in Heterozygous Familial Hypercholesterolemia(Atherosclerosis, clinical-9 (H) PE40,Poster Session (English),The 70th Anniversary Annual Scientific Meeting
- Identification of two novel missense mutations (p.R1221C and p.R1357W) in the ABCC6 (MRP6) gene in a Japanese patient with pseudoxanthoma elasticum (PXE)
- PE-285 J-LIT (Japan Lipid Intervention Trial) Score Predicts Recurrence of Coronary Event(Preventive medicine/Epidemiology/Education-4 (H) PE48,Poster Session (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- OE-101 Relationship of lipoprotein lipase and hepatic triacylglycerol lipase activity to serum adiponectin levels in Japanese hyperlipidemic men(Cerebrovascular circulation/Stroke-1 (H) OE17,Oral Presentation (English),The 70th Anniversary Annual Scientif
- Type III hyperlipoproteinemia exaggerated by Sheehan's syndrome with advanced systemic atherosclerosis - A 28-year clinical course
- 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)
- 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)
- Association Between ABCG5/G8 SNPs and Higher Cholesterol Absorption Marker in Hypercholesterolemia(Lipid Disorders 3 (H), 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
- Japan Lipid Intervention Trial (J-LIT) Chart Predicts the Absence of Coronary Artery Disease More Accurately Than Symptom Limited Exercise Stress Electrocardiography
- In-hospital Outcome in Octogenarians with Acute Coronary Syndrome Undergoing Emergent Coronary Angiography
- Gene mutations in adult Japanese patients with dilated cardiomyopathy
- Oxidative Stress Correlates with Left Ventricular Volume after Acute Myocardial Infarction
- 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-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
- 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
- Clinical Characteristics of Patients with Cardiopulmonary Arrest on Arrival in Acute Myocardial Infarction(Acute Myocardial Infarction, Clinical (Pathophysiology) 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-297 Clinacal Characteristics of Patients with Cardiopulmonary Arrest on Arrival in Acute Myocardial Infarction(Acute Myocardial Infarction, Clinical (Pathophysiology) 5 (IHD) : OJ35)(Oral Presentation (Japanese))
- Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease
- 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
- 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)
- The Relation between Cell Adhesion Molecules and Late Lumen Loss(Restenosis after Angioplasty, Basic/Clinical 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Difference in the risk factors for coronary, renal and other peripheral arteriosclerosis in heterozygous familial hypercholesterolemia
- FRS-128 Mutations in Phospholamban Gene Cause Hypertrophic and Dilated Cardiomyopathy(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Increased Circulating Matrix Metalloproteinase-2 in Patients with Hypertrophic Cardiomyopathy with Systolic Dysfunction
- Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
- PJ-425 Early Development of Dilated Cardiomyopathy in Subjects with Mutations in the Cardiac Troponin Complex Genes(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- OJ-511 Missense Mutations in Cardiac Ryanodine Receptor Gene Cause Hypertrophic Cardiomyopathy Associated with Ventricular Arrhythmia or Massive Hypertrophy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
- OJ-229 Atrial Fibrillation in Patients with Hypertrophic Cardiomyopathy with Different Genotypes(Cardiomyopathy, Clinical 1 (M) : OJ26)(Oral Presentation (Japanese))
- OJ-078 Usefulness of Q-T Peak Dispersion for Diagnosis of KCNH2 Gene Mutations in Patients with Long QT Syndrome(Arrhythmia, Basic 1 (A) : OJ10)(Oral Presentation (Japanese))
- FRS-129 Mutations Responsible for Dilated Cardiomyopathy in Japan(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- PJ-596 Exercise-induced Systolic Dysfunction in Patients with Non-obstructive Hypertrophic Cardiomyopathy and Mutations in the Cardiac Troponin Genes(Cardiomyopathy, Clinical 7 (M) : PJ100)(Poster Session (Japanese))
- OJ-335 PRKAR1A Gene Mutation in Patients with Cardiac Myxoma(Valvular Heart Disease/Pericarditis/Cardiac Tumor 2 (M) : OJ40)(Oral Presentation (Japanese))
- Alterations in Echocardiographic Tissue Characterization in Patients with Cardiac Troponin I Gene Mutation a Possible Indicator of Preclinical Hypertrophic Cardiomyopathy
- Cardiac Actin and Alpha-Tropomyosin Genes Are Associated with Neither Hypertrophic Nor Dilated Cardiomyopathy in Patients from Hokuriku District in Japan
- PE-280 Missense Mutations in the MYBPC3 Gene are Responsible for Hypertrophic Cardiomyopathy with Left Ventricular Systolic Dysfunction and Dilatation(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- PE-278 Electrocardiography Shows Preferable Diagnostic Value Even in Carriers of Hypertrophic Cardiomyopathy who do not Manifest Ventricular Wall Hypertrophy on Echocardiography(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- OJ-237 KCNJ2 Gene Mutation is a Rare Cause of Long QT Syndrome(Arrhythmia, Diagnosis/Pathophysiology/EPS 9 (A) : OJ27)(Oral Presentation (Japanese))
- FRS-132 Phenotypic Discrepancies Between Electrocardiography and Echocardiography for Hypertrophic Cardiomyopathy in Genetically Affected Subjects(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Left ventricular dysfunction and dilatation in elderly patients with hypertrophic cardiomyopathy associated with a novel missense mutation in MyBP-C gene
- Relationship between QT Variables and Disproportion of Left Ventricular Wall in Patients with Hypertrophic Cardiomyopathy
- Fluctuation of T-peak to T-end before and after ventricular tachycardia
- Q-T peak dispersion in congenital long QT syndrome ; increased lag of T wave peak as a new marker of HERG
- OE-057 Genetic Effects of Farnesoid-X-receptor on BMI, HDL-C, LDL-C and Development of Fatty Liver(Lipid disorders-1 (H) OE10,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- Pathophysiological Roles of the Adrenal Renin-Angiotensin System in Patients with Primary Aldosteronism
- Effects of Aldosterone Blockade on Cardiac Renin-Angiotensin-Aldosterone System in Salt-Sensitive Hypertension (Hypertension, Basic 5 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Probucol-Induced Long QT Syndrome Associated with a Novel Missense Mutation M124T in the N Terminus of HERG
- Long QT Syndrome Mutations in Different Sites of HERG Elicit a Variety of Functional Changes
- Double Missense Mutations (D611Y in KCNQ1 and D609G in HERG) in a Japanese Family with Long QT Syndrome
- Characterization of a Novel Missense Mutation E637K in the Pore-S6 Loop of HERG in a Patient with Long QT Syndrome
- Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome
- Crow-Fukase syndrome associated with high-output heart failure
- Sixteen-slice computed tomography, transthoracic real-time 3-dimensional echocardiography and magnetic resonance imaging assessment of a long-term survivor of rupture of sinus of valsalva aneurysm
- Increased matrix metalloproteinase-2 in patients with hypertrophic cardiomyopathy with systolic dysfunction
- CLINICAL CHARACTERISTICS OF PATIENTS WITH LEFT MAIN CORONARY ARTERY HIGH GRADE STENOSIS
- OJ-415 Electrocardiographic Events and Cholesterol Reduction with Pravastatin in Patients with Hypercholesterolemia : Hokuriku Lipid Coronary Heart Disease Study-Pravastatin Atherosclerosis Trial(Preventive Medicine/Epidemiology/Education 3 (H) : OJ50)(Or
- PCSK9 Gene Mutation is Less Frequent in Clinically Diagnosed FH Patients without LDLR and ApoB-100 Gene Mutation in Japan(Lipid Disorders 1 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Usefulness of Acoustic Densitometry Method for Detection of Myocardial Changes in Preclinical Patients with Hypertrophic Cardiomyopathy
- Difference in Coronary Blood Flow Dynamics between Patients with Hypertension and Those with Hypertrophic Cardiomyopathy
- Q-T peak dispersion in congenital long QT syndrome: Possible marker of mutation of HERG
- Cardiac Manifestations and Long-Term Course in Emery-Dreifuss Muscular Dystrophy Caused by a Nonsense Mutation in the STA Gene
- Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome
- A novel de novo mutation in the cardiac β - myosin heavy chain gene in patients with dilated cardiomyopathy
- Mitochondrial DNA mutations in hypertrophic cardiomyopathy
- Novel KCNQ1 missense mutation (D611Y) in a Japanese long QT family
- Whole and regional variation of cardiac sympathetic nervous activity in patients with hypertrophic cardiomyopathy with malignant tachyarrthythmias and sudden death
- Association between Single Nucleotide Polymorphisms (SNPs) of Cardiac Potassium Channel Genes and Drug-Induced Long QT Syndrome in Japanese
- A Novel Mutation (lnt21DSG+1A) in the MyBP-C Gene Shows Hypertrophic Cardiomyopathy with a High Degree of Penetrance in Adult Patients
- Diagnostic Values of Abnormal Q Waves for Hypertrophic Cardiomyopathy Based on the Genetic Information
- QT Variables in Preclinical Patients with Hypertrophic Cardiomyopathy
- QT Variables in Various Genotyped Patients with Hypertrophic Cardiomyopathy
- Mitochondrial DNA Mutations in Hypertrophic Cardiomyopathy
- Frequency of Asymmetric Septal Hypertrophy in Patients with Hypertrophic Cardiomyopathy : Difference in Genotypes
- Differences in Diagnostic Values of Abnormal Q Waves between Hypertrophic Cardiomyopathy with a cTnl Gene Mutation and MyBP-C Gene Mutations
- Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-pore site of SCN5A(Arrhythmia, Diagnosis/Pathophysiology/EPS 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-144 A Novel Missense Mutation of SCN5A Gene Associated with Brugada Syndrome by Bidirectional Effects on Blocking Actions of Antiarrhythmic Drugs(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- SCN5A Gene Mutations and Clinical Characteristics in Patients With Brugada-Type Electrocardiogram
- Brugada Syndrome With Ventricular Tachycardia and Fibrillation Related to Hypokalemia