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福井心臓血圧センター | 論文
- 353 乳児期大動脈縮窄症の外科治療
- Diagnostic Values of Abnormal Q Waves for Hypertrophic Cardiomyopathy Based on the Genetic Information
- QT Variables in Preclinical Patients with Hypertrophic Cardiomyopathy
- QT Variables in Various Genotyped Patients with Hypertrophic Cardiomyopathy
- Mitochondrial DNA Mutations in Hypertrophic Cardiomyopathy
- Frequency of Asymmetric Septal Hypertrophy in Patients with Hypertrophic Cardiomyopathy : Difference in Genotypes
- OE-038 Coronary Endothelial Dysfunction Pleiotropically Accelerates Atherothrombogenic Processes in Patients with Coronary Artery Disease(Angina Pectoris, Basic and Clinical (IHD) : OE5)(Oral Presentation (English))
- Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-pore site of SCN5A(Arrhythmia, Diagnosis/Pathophysiology/EPS 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-144 A Novel Missense Mutation of SCN5A Gene Associated with Brugada Syndrome by Bidirectional Effects on Blocking Actions of Antiarrhythmic Drugs(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- PE-138 Benidipine, a Long-Acting Calcium Channel Blocker, Improves Coronary Flow Reserve and Endothelial Function in Patients With Hypertension and Diabetes Mellitus(Coronary Circulation, Basic/Clinical 1 (IHD) : PE24)(Poster Session (English))
- Emergent thoracic aortic angioplasty and stenting for middle aortic syndrome in non-specific aortitis