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

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概要

• 論文の詳細を見る
• 2005-08-01

著者

• 清水 美妃子

  Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University

• INAI KEI

  Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University

• NAKAZAWA MAKOTO

  Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University

• Nakazawa Makoto

  Pediatric And Lifelong Congenital Cardiology Institute Southern Tohoku General Hospital

• Inai Kei

  Pediatric Cardiology The Heart Institute Of Japan Tokyo Women's Medical University

• 清水 美妃子

  Pediatric Cardiology The Heart Institute Of Japan Tokyo Women's Medical University

• Nakazawa Makoto

  Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University

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
• 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)
• 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
• 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

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