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Department of Cardiology, Fukui Prefectural Hospital | 論文
- PJ-540 Risk of Surgery after Coronary Drug-Eluting Stent Implantation(PJ091,Coronary Revascularization, PCI (DES) 3 (IHD),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- Cutoff Point Separating Affected and Unaffected Familial Hypercholesterolemic Patients Validated by LDL-receptor Gene Mutants
- Gene mutations in adult Japanese patients with dilated cardiomyopathy
- Coronary lesion morphology and prognosis in young males with myocardial infarction with or without familial hypercholesterolemia
- Diagnostic usefulness of the post-exercise systolic blood pressure response for the detection of coronary artery disease in patients with diabetes mellitus
- The first reported case of spotted fever in Fukui Prefecture, the northern part of central Japan
- Distribution of QTc Values and Prevalence of Short QT Syndrome in the Japanese Population (ECG/Body Surface Potential Mapping/Holter 6 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Gene Mutations in Patients with Hypertrophic Cardiomyopathy Showing Mild Left Ventricular Hypertrophy(Cardiomyopathy, Clinical 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Differences in Diagnostic Value of Classic Electrocardiographic Voltage Criteria for Hypertrophic Cardiomyopathy in a Genotyped Population(Cardiomyopathy, Clinical 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Ankyrin-B Gene Mutation is a Rare Cause of Long QT Syndrome in Japan(Arrhythmia, Basic 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Long-Term Course of Patients with Cardiomyopathy Associated with Phospholamban Gene Mutations(Cardiomyopathy, Clinical 8 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Early Development of Dilated Cardiomyopathy in Subjects with Hypertrophic Cardiomyopathy Caused by Mutations of the Thin Filament Genes(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Angiotensin II Type 1 Receptor A/C1166 Gene Polymorphism and Left Ventricular Systolic Dysfunction in Hypertrophic Cardiomyopathy with Sarcomere Gene Mutations(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation
- Impact of Bundle-Branch Block on Clinical Manifestation in Patients with Hypertrophic Cardiomyopathy : Analyses Based on Molecular Genetic Diagnoses(Cardiomyopathy, Clinical 6 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-128 Mutations in Phospholamban Gene Cause Hypertrophic and Dilated Cardiomyopathy(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Paroxysmal Atrial Fibrillation due to Bronchogenic Cyst
- Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
- Prevalence and Onset of Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 6 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-425 Early Development of Dilated Cardiomyopathy in Subjects with Mutations in the Cardiac Troponin Complex Genes(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- OJ-335 PRKAR1A Gene Mutation in Patients with Cardiac Myxoma(Valvular Heart Disease/Pericarditis/Cardiac Tumor 2 (M) : OJ40)(Oral Presentation (Japanese))
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