スポンサーリンク
The Gene Cardiovascular Disease Epidemiology Committee Of Japanese Pediatric Cardiology And Cardiac | 論文
- Nationwide Survey of Management of Pregnancy and Delivery in Women with Cardiovascular Disease : in 2002 and 2003(Cardiovascular Preventive Medicine (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Arrhythmia in Patients with Congenital Heart Disease during Pregnancy(Diagnosis and Management of Arrhythmias in Adults with Congenital Heart, The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Arrhythmia and Conduction Disturbances in Patients With Congenital Heart Disease During Pregnancy : Multicenter Study
- Survey of Prophylaxis and Management of Infective Endocarditis in Patients With Congenital Heart Disease : Japanese Nationwide Survey
- Cardiac arrhythmias in women with congenital heart disease : Japanese multicenter survey
- Current Characteristics of Infective Endocarditis in Japan : An Analysis of 848 Cases in 2000 and 2001
- PJ-333 Outcome of Pregnancy in Women After the Fontan Procedure(Congenital heart disease/Kawasaki's disease-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-741 Risk Factors for Fortality During Infective Endocarditis in Pediatric and Adult Patients with Congenital Heart Diseases(Congenital heart disease/Kawasaki's disease-3 (M) PJ126,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting
- 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
- Mortality From Congenital Cardiovascular Malformations in Japan, 1968 Through 1997
- Risk factors for arrhythmia late 5 to 30 years after repair of tetratogy of Fallot : a Japanese multi-centre study
- Successful Cardiac Resynchronization Therapy in a 3-Year-Old Girl With Isolated Left Ventricular Non-Compaction and Narrow QRS Complex : A Case Report
- Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease
- PE-306 SCN5A Variant in Japanese Patients with Left Ventricular Noncompaction and Arrhythmia(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- A Common Mitochondrial 16189 DNA Variant Associated with Left Ventricular Hypertrophy in Type 2 Diabetes Mellitus
- Novel LAMP-2 Mutation in a Family With Danon Disease Presenting With Hypertrophic Cardiomyopathy
- Evaluation of left ventricular volume using automatic border detection in children : A comparison with conventional off-line echocardiographic quantification
- FRS-059 Phenotypic and Genotypic Analysis in Familial Atrial Septal Defect(Oxidative Stress, Autonomic Function and Peripheral Vascular Diseases (H) : FRS7)(Featured Research Session (English))
- Implications of Mutations of Activin Receptor-Like Kinase 1 Gene (ALK1) in Addition to Bone Morphogenetic Protein Receptor II Gene (BMPR2) in Children With Pulmonary Arterial Hypertension
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