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福井心臓血圧センター | 論文
- 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))
- Alterations in Echocardiographic Tissue Characterization in Patients with Cardiac Troponin I Gene Mutation a Possible Indicator of Preclinical Hypertrophic Cardiomyopathy
- Cardiac Actin and Alpha-Tropomyosin Genes Are Associated with Neither Hypertrophic Nor Dilated Cardiomyopathy in Patients from Hokuriku District in Japan
- Can LQT1 be Differentiated with ST-T Morphology from the Other Type of Long QT Syndrome?(Arrhythmia, Diagnosis/Pathophysiology/EPS 6 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Prevalence of Gene Mutations in Patients with Congenital Long QT Syndrome(Arrhythmia, Basic 2 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- 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))
- OE-057 Genetic Effects of Farnesoid-X-receptor on BMI, HDL-C, LDL-C and Development of Fatty Liver(Lipid disorders-1 (H) OE10,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- 25)偶然に発見された陳旧性心筋梗塞の小児例 : 日本循環器学会第52回北陸地方会
- OJ-415 Electrocardiographic Events and Cholesterol Reduction with Pravastatin in Patients with Hypercholesterolemia : Hokuriku Lipid Coronary Heart Disease Study-Pravastatin Atherosclerosis Trial(Preventive Medicine/Epidemiology/Education 3 (H) : OJ50)(Or
- Usefulness of Acoustic Densitometry Method for Detection of Myocardial Changes in Preclinical Patients with Hypertrophic Cardiomyopathy
- Prevalence of Long QT Syndrome in Japanese Children(ECG/Body Surface Potential Mapping/Holter 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- 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
- 11)出産を経験した後,平穏に経過,肺出血で突然死したTruncus Arteriosusの1例 : 日本循環器学会第51回北陸地方会
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