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Department Of Pediatric Cardiology | 論文
- Long-term Results after Surgical Repair of Total Anomalous Pulmonary Venous Connection : Hemodynamic Evaluation of Pulmonary Venous Obstruction with Isoproterenol Infusion
- PREDICTION OF QUALITY OF LIFE AT LONG-TERM FOLLOW-UP AFTER FONTAN OPERATION BY SCORING RISK FACTORS
- -123- ANGIOGRAPHIC MORPHOLOGY OF PULMONARY ARTERIES IN VENTRICULAR SEPTAL DEFECT ASSOCIATED WITH PULMONARY ATRESIA : Congenital Heart Disease, Kawasaki Disease : FREE COMMUNICATIONS(I) : PROCEEDINGS OF THE 51th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CI
- PULMONARY HYPERTENSION IN COMPLETE TRANSPOSITION OF THE GREAT ARTERIES ASSOCIATED WITH VENTRICULAR SEPTAL DEFECT : Congenital Heart Disease : PROCEEDINGS OF THE 50th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- JUXTA-DUCTAL LEFT PULMONARY ARTERY STENOSIS IN PULMONARY ATRESIA : ANGIOGRAPHIC FINDINGS, NATURAL HISTORY AND MORPHOGENESIS : Congenital Heart Disease, Kawasaki Disease : FREE COMMUNICATIONS (VI) : PROCEEDINGS OF THE 49th ANNUAL SCIENTIFIC MEETING OF THE
- NATURAL HISTORY OF SUBARTERIAL INFUNDIBULAR VENTRICULAR SEPTAL DEFECT : Congenital Heart Disease, Kawasaki Disease : IV : 48 Annual Scientific Meeting, Japanese Circulation Society
- AORTOGRAPHY OF PULMONARY VESSELS IN PULMONARY ATRESIA, VENTRICULAR SEPTAL DEFECT AND MAJOR AORTOPULMONARY COLLATERAL ARTERIES : Congential Heart Disease : 46th Annual Scientific Meeting, Japanese Circulation Society
- Vasodilating Effect and Tissue Accumulation of Prostaglandin E_1 Incorporated in Lipid Microspheres on the Rat Ductus Arteriosus
- Histopathologic aspects of endomyocardial biopsy in pediatric patients with idiopathic ventricular tachycardia
- Transcatheter Occlusion of Patent Ductus Arteriosus With a New Detachable Coil System(DuctOcclud) : a Multicenter Clinical Trial
- Balloon Angioplasty for Aortic Coarctation : Report of a Questionnaire Survey by the Japanese Pediatric Interventional Cardiology Committee
- -127- QUANTITATIVE ANALYSIS OF COMMON ATRIO-VENTRICULAR VALVE FUNCTION IN SINGLE VENTRICLE : Congenital Heart Disease, Kawasaki Disease : FREE COMMUNICATIONS(I) : PROCEEDINGS OF THE 51th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- -1039-ELECTROCARDIOGRAPHIC FINDINGS OF FASCICULOVENTRICULAR CONNECTION DIAGNOSED FROM HEALTHY QV1 STUDENTS : THE 54th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- PJ-735 The Same Mutations in the Cardiac Troponin T Gene Show Various Prognoses in Japanese Patients with Hypertrophic Cardiomyopathy(Cardiac hypertrophy, basic/clinical-4 (M) PJ125,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting
- A Case of Williams Syndrome with Balanced Translocation t (1; 7) (q43; q31) and Regional Deletion at 7q11.23
- IS091 Electrophysiological properties of the mutant HERG channel (G601S) expressed in mammalian cells
- 0720 Genetic analysis of familial long QT Syndrome : Missense mutation in HERG in LQT2 family
- -0409- Abnormalities of Chromosome 7 Associated with Williams Syndrome and Supravalvular Aortic Stenosis(PROCEEDINGS OF THE 59th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY)
- CHARACTERIZATION AND DEFFERENTIAL EXPRESSION OF CULTURED VASCULAR SMOOTH MUSCLE MYOSHIN HEAVY CHAIN GENE INDUCED BY cAMP
- -0397- TETRALOGY OF FALLOT ASSOCIATED WITH CHROMOSOME 22q11 DELETION.(PROCEEDINGS OF THE 59th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY)
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