Incomplete Atrioventricular Septal Defect With Hypoplastic Left Ventricle and Left Atrioventricular Valve Stenosis

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概要

• 論文の詳細を見る
• 2001-04-10

著者

• YAMAGISHI Masaaki

  the Department of Cardiovascular Surgery, Children's Research Hospital, Kyoto Prefectural University

• FUJIWARA Katsuji

  the Department of Cardiovascular Surgery, Children's Research Hospital, Kyoto Prefectural University

• KITAMURA Nobuo

  the Department of Cardiovascular Surgery, Children's Research Hospital, Kyoto Prefectural University

• YOSHIDA Masahiro

  the Department of Cardiovascular Surgery, National Cardiovascular Center

• Fujiwara Katsuji

  The Department Of Pediatric Cardiovascular Surgery Children's Research Hospitel Kyoto Prefectur

• Yamagishi Masaaki

  The Department Of Pediatric Cardiovascular Surgery Children's Research Hospitel Kyoto Prefectur

• Kitamura Nobuo

  The Department Of Pediatric Cardiovascular Surgery Children's Research Hospitel Kyoto Prefectur

• NISHIMURA Motohiro

  the Department of Pediatric Cardiovascular Surgery, Children's Research Hospitel, Kyoto Prefectural

• Nishimura Motohiro

  The Department Of Pediatric Cardiovascular Surgery Children's Research Hospitel Kyoto Prefectur

• Yoshida Masahiro

  The Department Of Atherosclerosis And Diabetes National Cardiovascular Center

関連論文

• OJ-134 Aldosterone, but Not Angiotensin II, Reduces Angiotensin Converting Enzyme 2 Gene Expression Levels in Cultured Neonatal Rat Cardiomyocytes(OJ23,Hypertension, Basic (H),Oral Presentation (Japanese),The 73rd Annual Scientific Meeting of The Japanese
• Aldosterone, but Not Angiotensin II, Reduces Angiotensin Converting Enzyme 2 Gene Expression Levels in Cultured Neonatal Rat Cardiomyocytes
• PJ-321 Clinical Factors Affecting Serum Potassium Concentration(Heart failure, clinical(16)(M),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
• OE-295 Coronary Microvessel Spasm is a Frequent Cause of Myocardial Ischemia in Postmenopausal Women with Angina-like Chest Pain(OE50,Coronary Circulation/Chronic Coronary Disease (Basic/Clinical) (IHD),Oral Presentation (English),The 73rd Annual Scientif
• NRSF Is Involved in Molecular Pathways for Sudden Death Associated with Heart Failure
• PJ-530 Post Procedural Creatinine Increase is Associated with Endothelial Dysfunction in Patients with Early Stage of Chronic Kidney Disease(PJ089,Atherosclerosis (Clinical/Pathophysiology) 1 (IHD),Poster Session (Japanese),The 73rd Annual Scientific Meet
• OE-389 Clinical Phenotype of Japanese LQT1 Form of Congenital Long QT Syndrome by Location and Coding Type From Japanese Multicenter Registry(Arrhythmia, diagnosis/Pathophysiology/EPS(02)(A),Oral Presentation(English),The 72nd Annual Scientific Meeting of
• 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))
• Comparison of Thrombolytic Therapies With Mutant tPA(Lanoteplase/SUN9216)and Recombinant tPA(Alteplase)for Acute Myocardial Infarction
• IS040 Positive association between essential hypertension and Glu298Asp polymorphism in the endothelial nitric oxide synthase gene
• Captopril Reduced Plasminogen Activater Inhibiter Activity in Patients With Acute Myocardial Infarction
• 1 Molecular Basis for Low Penetrance in the Long QT Syndrome(Meet the Expert 7 (ME7) (A) : Issues on Sudden Cardiac Death)(Special Program)
• OJ-011 Association of Obesity Related Factors with Plasma B-type Natriuretic Peptide Levels in General Japanese Population(OJ02,Obesity/SAS (H),Oral Presentation (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
• Impact of Metabolic Syndrome Components on the Incidence of Cardiovascular Disease in a General Urban Japanese Population : The Suita Study
• Leptin Gene and Leptin Receptor Gene Polymorphisms Are Associated with Sweet Preference and Obesity
• FRS-076 A link between LDL Receptor (LDLR) Gene Mutation and Clinical Manifestations in Familial Hypercholesterolemia(FRS16,Basic Mechanisms of Lipid Disorders and Metabolic Syndrome (H),Featured Research Session (English),The 73rd Annual Scientific Meeti
• PJ-898 Predicting high risk patients of coronary artery disease in heterozygous familial hypercholesterolemia from clinical features(Lipid disorders(05)(H),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
• PE-104 Severer Phenotypes of Long QT Syndrome are Associated with Compound Mutations : A Multicenter Study(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Soci
• Mutation Site Dependent Variability of Cardiac Events in Japanese LQT2 Form of Congenital Long-QT Syndrome
• PJ-671 Abdominal Obesity is a Significant Determinant of Endothelial Dysfunction in High Risk Patients with or without Metabolic Syndrome(Diabetes / Obesity / Metabolic syndrome(13)(H),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Jap
• PJ-119 Synergistic Interaction of Plasma BNP and Glucose Levels for Enhanced Risk for Cardiovascular Re-attacks in Patients with Heart Failure(Heart failure, clinical(13)(M),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circu
• 3 Mutant KCNE3 Reduces Repolarizing Potassium Current And Causes Long QT Syndrome(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
• PE-103 Clinical Phenotype of Japanese LQT3 Form of Congenital Long QT Syndrome by Location of Mutation from Japanese Multicenter Registry(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting o
• FRS-117 Clinical and Electrocardiographic Characteristics of Japanese Probands with Brugada Syndrome with an SCN5A Mutation from Japanese Multicenter Registry(FRS24,Novel Mechanisms of Ventricular Arrhythmia (A),Featured Research Session (English),The 73r
• PJ-208 Impact of Frameshift Mutation and Nonsense-mediated mRNA Decay on Clinical Phenotype in LQT2 Form of Congenital Long QT Syndrome(Arrhythmia,diagnosis/Pathophysiology/EPS(13)(A),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japa
• OJ-061 Association analysis between autosomal recessive hypercholesterolemia (ARH) gene and hypercholesterolemia(Lipid Disorders 1 (H) : OJ8)(Oral Presentation (Japanese))
• Association of insulin resistance with endothelial dysfunction and common carotid artery wall thickening in essential hypertension
• Repair of Partial Anomalous Pulmonary Venous Connection With a Minimal Atriotomy
• 5 Cellular Mechanism, Gender and Ethnic Difference in the Brugada Syndrome(Symposium 5 (SY-05) (A) New Findings of Mechanism and Therapeutic Strategies of Idiopathic Ventricular Fibrillation,Special Program,The 72nd Annual Scientific Meeting of the Japane
• 2 Mutation Location- or Mutation Type-Specific Clinical Severity and Therapy in LQT1 and LQT2 Forms of Congenital Long-QT Syndrome(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Meeting
• PJ-378 Decreased Circulating CD34-positive Cells are Associated with High Plasma BNP Concentration in Elderly Patients with Type 2 Diabetes Mellitus(Diabetes/Obesity/Metabolic syndrome-9 (H) PJ64,Poster Session (Japanese),The 70th Anniversary Annual Scien
• Obesity and Insulin Resistance Possibly Promotes Ischemic Heart Disease of the Patients with Familial Combined Hyperlipidemia (FCHL)(Lipid Disorders 4 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• OJ-327 Fluvastatin Increases Transcriptional Activity of the Endothelial Nitric Oxide Synthase Gene, Especially With -786T/C Polymorphism(Cardiovascular Pharmacology, Basic/Clinical 2 (H) : OJ39)(Oral Presentation (Japanese))
• FRS-041 Direct sequencing based on precise characterization of clinical phenotype is sufficient for genotyping of congenital Long QT syndrome(Arrhythmia-Clinical : Advances in Diagnosis and Management (A) : FRS5)(Featured Research Session (English))
• Differential Gene Expression in Myocardial Infarction in Diabetic Obese Mice
• Epinephrine Test for Genotyping LQT1 and LQT2 Forms of Congenital Long QT Syndrome
• IS003 Differing role of Extracellular signal-regulated kinase in endothelin-1-induced and cardiotrophin-1-induced hypertrophic signals in cultured cardiac myocytes
• IS049 Implication of cardiotrophin-1 in myocyte-nonmyocyte interaction during cardiac hypertrophy in vitro
• FRS-116 Circulating Class A Macrophage Scavenger Receptor Positive Circulating Mononuclear Cells Were Specifically Increased in Patients with Acute Coronary Syndrome(Novel Aspects for Acute Coronary Syndrome(IHD),Featured Research Session,The 72nd Annual
• Predominant Effect of A-Type Natriuretic Peptide on Reduction of Oxidative Stress During the Treatment of Patients With Heart Failure
• PJ-799 A Predominant Effect on A-type Natriuretic Peptide on Reduction of Oxidative Stress during the Treatment of Patients with Heart Failure(Heart failure, clinical-18, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• PJ-616 A Novel Genetic Marker for Coronary Spasm in Women from a Genome-Wide Analysis(Genetics/Genetically engineered models/Gene therapy-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• OE-377 The-786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene is Associated with Calcium Channel Blocker Resistant Coronary Spasm(Angina pectoris, basic/clinical-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• PJ-767 Contribution of Endogenous Natriuretic Peptides to the Therapeutic Effect of Carperitide Infusion in Acute Heart Failure(Heart failure, clinical-20 (M) PJ133,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese C
• PJ-220 Direct Effects of Aldosterone on Cardiomyocytes in the Presence of Normal and Elevated Extracellular Sodium(Hypertension, basic-3 (H) PJ37,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
• PE-005 Gene Expression Profile of Circulating Mononuclear Cells in Patients with Acute Coronary Syndrome(Acute coronary syndrome, basic/clinical-4 (IHD) PE1,Poster Session (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulatio
• OJ-339 Genetic Analysis for Coronary Spasm Using Multiple Candidate Gene Polymorphisms(Genetics/Genetically engineered models/Gene therapy-1 (M) OJ57,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation S
• Difference between Fluvastatin and Simvastatin on the eNOS Gene Expression (Cardiovascular Pharmacology, Basic/Clinical 2 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Association of the Endothelial Nitric Oxide Synthase Gene Polymorphisms and Myocardial Contractility (Genetics/Genetically Engineered Models (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Reduction in Gene Expression of Angiotensin Converting Enzyme 2 by Aldosterone in Neonatal Rat Cardiomyocytes(Heart Failure, Clinical 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Venous Infusion of A-type Natriuretic Peptide Reduced Oxidative Stress in Patients with Heart Failure(Heart Failure, Clinical 11 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Elevation of Plasma Levels of ACTH and Aldosterone in Patients with Essential Hypertension; Possible Roles in Low Renin Hypertension
• Activation of Proopiomelanocortin Gene Expression in Failing Human Heart
• Paradoxical Secretion of Aldosterone and DHEA from the Human Heart
• Possible Cardioprotective Effect of Dehydroepiandrosterone Produced in the Human Heart
• Aldosterone Induces Angiotensin-Converting-Enzyme Gene Expression through Both Mineralcorticoid -and Glucocorticoid- Receptors in Cultured Neonatal Rat Cardiocytes
• Inhibitory Effect of Natriuretic Peptides on Aldosterone Synthase Gene Expression in Cultured Neonatal Rat Cardiocytes
• Plasma B-Type Natriuretic Peptide as a Prognostic Marker of Myocardial Infarction : Ten Years Follow-Up Study
• Increased Risk of Coronary Spasm Due to the Combination of T^ to C Mutation in the eNOS Gene and Smoking
• Increased risk of coronary spasm due to the combination of-786T to C mutation in eNOS gene and smoking
• Detection of CYP17 gene expression and the regulatory mechanisms in human vascular smooth muscle cells
• Proopiomelanocortin (POMC) gene expression in the human autopsy heart
• Isocaloric High-protein Diet Ameliorates Systolic Blood Pressure Increase and Cardiac Remodeling Caused by Maternal Caloric Restriction in Adult Mouse Offspring
• PE-341 Improvement of Endothelial Function is a Potential Clinical Target for Heart Failure Patients with Systolic or Diastolic Dysfunction(Heart failure, clinical(10)(M),Poster Session(English),The 72nd Annual Scientific Meeting of the Japanese Circulati
• Mitral Valve Plasty in Systemic Lupus Erythematosus in the Setting of Antiphospholipid Syndrome
• Production of dehydroepiandrosterone (DHEA) in the human heart : Comparison between control subjects and heart failure patients
• 2 Future Challenge in Brugada syndrome : Gender and Ethnic Differences(Brugada Syndrome:From Cell to Bedside,Plenary Session 2 (PL2) (A),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
• PJ-243 A Novel Mutation in the Autosomal Recessive Hypercholesterolemia Gene Leads to Hypercholesterolemia(Lipid disorders-3 (H) PJ41,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
• Resistin Gene Polymorphism Positively Associated with the Metabolic Syndrome in Japanese Men(Gene Therapy/Genetic Engineering (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• PJ-076 Differences in the Frequencies of -786T/C Polymorphism of the eNOS Gene and in the Promoter Activity : Caucasian and Japanese(Genetics/Genetically Engineered Models 1 (H) : PJ13)(Poster Session (Japanese))
• Class A Macrophage Scavenger Receptors Gene Expression Levels and Acute Coronary Syndrome(Acute Coronary Syndrome/Changing Strategy (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Pump failure death and sudden cardiac death in patients with cardiac dysfunction : A search for prognostic predictive factors-A long-term follow-up study
• Oblique Plication for Repair of the Atrialized Ventricle and Tricuspid Incompetence of Ebstein's Anomaly
• The combined impact of blood pressure category and glucose abnormality on the incidence of cardiovascular diseases in a Japanese urban cohort : the Suita Study
• Detection of Aldosterone Synthase Gene Expression in the Failing Human Ventricle : Quantitative Analysis Using a Newly Modified Real-Time RT-PCR
• Incomplete Atrioventricular Septal Defect With Hypoplastic Left Ventricle and Left Atrioventricular Valve Stenosis
• Face Image Recognition by 2-Dimensional Discrete Walsh Transform and Multi-Layer Neural Network(Source Coding/Imge Processing)(Information Theory and Its Applications)
• Detection of CYP17 gene expression and dehydroepiandrosterone production in the human heart
• Association of plasma B-type natriuretic peptide levels with obesity in a general urban Japanese population : the Suita study

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