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金沢大学 医学系研究科循環器内科学 | 論文

• PJ-656 A New Device for Transluminal Removal of Coronary Stent(Coronary revascularization, PCI(24)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
• PJ-366 Delayed Occurrence of Cerebrovascular Events After Severe Earthquake in Japan : Comparison With Cardiovascular Events(Preventive medicine/Epidemiology/Education(06)(H),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circ
• Cardiac Manifestations and Genotype-Phenotype Correlations in Carriers with the STA Gene Mutations(Myocardial Disease, Cardiomyopathy and Myocarditis (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))
• 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-511 Missense Mutations in Cardiac Ryanodine Receptor Gene Cause Hypertrophic Cardiomyopathy Associated with Ventricular Arrhythmia or Massive Hypertrophy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
• OJ-229 Atrial Fibrillation in Patients with Hypertrophic Cardiomyopathy with Different Genotypes(Cardiomyopathy, Clinical 1 (M) : OJ26)(Oral Presentation (Japanese))
• OJ-078 Usefulness of Q-T Peak Dispersion for Diagnosis of KCNH2 Gene Mutations in Patients with Long QT Syndrome(Arrhythmia, Basic 1 (A) : OJ10)(Oral Presentation (Japanese))
• FRS-129 Mutations Responsible for Dilated Cardiomyopathy in Japan(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
• PJ-596 Exercise-induced Systolic Dysfunction in Patients with Non-obstructive Hypertrophic Cardiomyopathy and Mutations in the Cardiac Troponin Genes(Cardiomyopathy, Clinical 7 (M) : PJ100)(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))
• PE-280 Missense Mutations in the MYBPC3 Gene are Responsible for Hypertrophic Cardiomyopathy with Left Ventricular Systolic Dysfunction and Dilatation(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
• PE-278 Electrocardiography Shows Preferable Diagnostic Value Even in Carriers of Hypertrophic Cardiomyopathy who do not Manifest Ventricular Wall Hypertrophy on Echocardiography(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
• OJ-237 KCNJ2 Gene Mutation is a Rare Cause of Long QT Syndrome(Arrhythmia, Diagnosis/Pathophysiology/EPS 9 (A) : OJ27)(Oral Presentation (Japanese))
• FRS-132 Phenotypic Discrepancies Between Electrocardiography and Echocardiography for Hypertrophic Cardiomyopathy in Genetically Affected Subjects(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
• Left ventricular dysfunction and dilatation in elderly patients with hypertrophic cardiomyopathy associated with a novel missense mutation in MyBP-C gene
• Relationship between QT Variables and Disproportion of Left Ventricular Wall in Patients with Hypertrophic Cardiomyopathy
• Fluctuation of T-peak to T-end before and after ventricular tachycardia
• Q-T peak dispersion in congenital long QT syndrome ; increased lag of T wave peak as a new marker of HERG

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