HEMODYNAMIC EFFECTS OF ISOPROTERENOL DURING EARLY STAGES OF MORPHOGENESIS, DIFFERENCE BETWEEN CHICK AND RAT EMBRYOS : Cardiovascular Drugs : 53 Annual Scientific Meeting, Japanese Circulation Society
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
- 1989-08-20
著者
-
Nakazawa Makoto
Pediatric And Lifelong Congenital Cardiology Institute Southern Tohoku General Hospital
-
Miyagawa Sachiko
Pediatric Cardiology The Heart Institute Of Japan Tokyo Women's Medical College
-
Takao Atsuyoshi
Pediatric Cardiology Heart Institute Of Japan Tokyo Women's Medical College
-
Takao Atsuyoshi
Pediatric Cardiology The Heart Institute Of Japan Tokyo Women's Medical College
-
Ikeda Kazuo
Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical College
-
Nakazawa Makoto
Pediatric Cardiology The Heart Institute Of Japan Tokyo Women's Medical College
-
Ikeda Kazuo
Pediatric Cardiology The Heart Institute Of Japan Tokyo Women's Medical College
関連論文
- 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
- ファロー四徴症児の無酸素発作予防のためのカテーテル前投薬におけるペチジンの有用性について : 後方視的検討および前方視的無作為検討の結果から
- 1 Molecular Basis for Low Penetrance in the Long QT Syndrome(Meet the Expert 7 (ME7) (A) : Issues on Sudden Cardiac Death)(Special Program)
- CHARACTERISTICS OF CARDIAC FUNCTION DURING EXERCISE IN PATIENTS WITH TA AFTER FONTAN'S OPERATION : Doppler, RI : I : 48 Annual Scientific Meeting, Japanese Circulation Society
- ELECTROPHYSIOLOGICAL STUDIES IN PATIENTS WITH ATRIOVENTRICULAR DISCORDANCE : PROCEEDINGS OF THE 47th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY : Electrophysiology (I)
- OJ-009 A Common KCNE1 Polymorphism, D85N, is a Genetic Modifier of Long QT Syndrome(Arrhythmia, diagnosis/ Pathophysiology/ EPS(03)(A),Oral Presentation(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- A single mutation of cardiac sodium channel gene confers phenotypes of both Brugada and long QT syndromes
- Ion channel mutations and polymorphisms in Japanese patients with acquired long QT syndrome
- 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
- Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms
- Risk Factors for Mortality and Morbidity in Patients with Cyanotic Congenital Heart Disease (Congenital Heart Disease/Kawasaki's Disease 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Arrhythmias Late After Repair of Tetralogy of Fallot : A Japanese Multicenter Study
- Effect of beraprost sodium on pulmonary vascular resistance in candidates for a Fontan procedure : A preliminary study
- An SCN5A Mutation Associated With Idiopathic Ventricular Fibrillation Alters The Na^+ Channel Pore Structure And Responses To Antiarrhythmic Drugs
- PJ-190 A KCNE1 Single Nucleotide Polymorphism, D85N, Serves as a Modifier in Forme-fruste Type of Long QT syndrome(Genetics/Genetically engineered models/Gene therapy-3 (M) PJ32,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of t
- Double SCN5A mutation underlying asymptomatic Brugada syndrome
- Single Nucleotide Polymorphisms of Cardiac Na^+ Channel Gene SCN5A : Allelic Prevalence in Brugada Syndrome and Their Biophysical Properties
- IS052 A mitochondrial DNA is responsible for the pathogenesis of congenital long QT syndrome
- ARRHYTHMIAS IN CORRECTED TRANSPOSITION OF THE GREAT ARTERIES, CORRELATION BETWEEN THE ARRHYTHMIAS AND ONSET-AGE, ASSOCIATED INTRACARDIAC ANOMALIES AND Pao_2 : PROCEEDINGS OF THE 37TH ANNUAL MEETING OF THE JAPANESE CIRCULATION SOCIETY
- High-risk for Bradyarrhythmic Complications in Patients with Brugada Syndrome Caused by SCN5A Gene Mutations(Arrhythmia, Basic (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- EPICARDIAL MAPPING PATTERNS IN CONGENITAL HEART DISEASES : Electrocardiography : IInd Auditorium : Proceedings of the 43rd Annual Meeting of the Japanese Circulation Society, Tokyo, 1979
- 5 Overlap Between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Meeting of the
- Increased P-Selectin Expression on Platelets and Decreased Plasma Thrombomodulin in Fontan Patients
- Aortic and Valvular Size in Patients with Aortic Regurgitation Long after Arterial Switch Operation in Transposition of the Great Arteries
- PE-307 Left Ventricular Noncompaction Associated With Mutations in Cardiac Na Channel Gene SCN5A(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OE-085 Genetic Factors Conferring Congenital Sick Sinus Syndrome in SCN5A Mutation Carriers(Arrhythmia, basic-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Sustained Ventricular Tachycardia and Late Potentials after Repair of Tetralogy of Fallot(Congenital Heart Disease/Kawasaki's Disease 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- 1 Genotype-Phenotypes Relations of SCN5A-Positive Brugada Syndrome(Brugada Syndrome:From Cell to Bedside,Plenary Session 2 (PL2) (A),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- EVALUATION OF LEFT VENTRICULAR FUNCTION IN PATIENTS AFTER JATENE PROCEDURE, A STUDY USING LEFT VENTRICULAR END-SYSTOLIC WALL STRESS-VELOCITY OF FIBER SHORTENING RELATION : Ventricular Function : 53 Annual Scientific Meeting, Japanese Circulation Society
- Guidelines for Diagnosis and Management of Cardiovascular Sequelae in Kawasaki Disease (JCS 2008) : Digest Version
- ANATOMIC TYPES OF UNI-VENTRICULAR HEART IN JAPANESE : PROCEEDINGS OF THE 38TH ANNUAL MEETING OF THE JAPANESE CIRCULATION SOCIETY
- REGULATION OF MYOSIN ATPase IN THE DEVELOPING HEART : Cardiac Metabolism : FREE COMMUNICATIONS (II) : PROCEEDINGS OF THE 49th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- Immunonutritional effects during synbiotics therapy in pediatric patients with short bowel syndrome
- HEMODYNAMIC EFFECTS OF ISOPROTERENOL DURING EARLY STAGES OF MORPHOGENESIS, DIFFERENCE BETWEEN CHICK AND RAT EMBRYOS : Cardiovascular Drugs : 53 Annual Scientific Meeting, Japanese Circulation Society
- Afterload Mismatch, and Cerebral Intraventricular and Pulmonary Hemorrhage in Preterm Infants
- OE-284 Oxygen Causes Contraction of the Ductus Arteriosus By Decreasing Intracellular H_2O_2 Generation(Congenital Heart Disease/Kawasaki's Disease 1 (M) : OE35)(Oral Presentation (English))
- Arrhyhtmias in Postoperative Cyanotic Congenital Heart Disease : -Japanese Experience-(ALTAS-CHD Study)(Diagnosis and Management of Arrhythmias in Adults with Congenital Heart, The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Guidelines for Risks and Prevention of Sudden Cardiac Death (JCS 2010) : Digest Version