スポンサーリンク
金沢大学 医学系研究科循環器内科学 | 論文
- Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome
- Q-T peak dispersion in congenital long QT syndrome: Possible marker of mutation of HERG
- Cardiac Manifestations and Long-Term Course in Emery-Dreifuss Muscular Dystrophy Caused by a Nonsense Mutation in the STA Gene
- Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome
- A novel de novo mutation in the cardiac β - myosin heavy chain gene in patients with dilated cardiomyopathy
- Mitochondrial DNA mutations in hypertrophic cardiomyopathy
- Novel KCNQ1 missense mutation (D611Y) in a Japanese long QT family
- Whole and regional variation of cardiac sympathetic nervous activity in patients with hypertrophic cardiomyopathy with malignant tachyarrthythmias and sudden death
- A Novel Mutation (lnt21DSG+1A) in the MyBP-C Gene Shows Hypertrophic Cardiomyopathy with a High Degree of Penetrance in Adult Patients
- Impact of Renin-Angiotensin System Polymorphisms on Development of Systolic Dysfunction in Hypertrophic Cardiomyopathy : Evidence From a Study of Genotyped Patients