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Division Of Cardiology Kanazawa Cardiovascular Hospital | 論文
- Hypoxic Preconditioning Induces the Expression of Heme Oxygenase-1 via P38 Mitogen-Activated Protein Kinase (p38MAPK) Pathway in Cardiac Fibroblasts
- OE-210 A New Method for Determining Functional LDL-C Receptor Activity in Hypercholesterolemic Patients : Application of CD3/CD28 Assay in Lymphocytes(Lipid disorders(01)(H),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Cir
- The Relation between Cell Adhesion Molecules and Late Lumen Loss(Restenosis after Angioplasty, Basic/Clinical 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Difference in the risk factors for coronary, renal and other peripheral arteriosclerosis in heterozygous familial hypercholesterolemia
- FRS-128 Mutations in Phospholamban Gene Cause Hypertrophic and Dilated Cardiomyopathy(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
- 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))
- 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))
- CLINICAL CHARACTERISTICS OF PATIENTS WITH LEFT MAIN CORONARY ARTERY HIGH GRADE STENOSIS
- PJ-038 The Correlation between Technetium 99m-sestamibi Myocardial Scintigraphy and Mitochondrial Cytochrome Oxidase Activity in Microvascular Angina(Nuclear Cardiology 3 (I) : PJ7)(Poster Session (Japanese))
- The correlation between technetium 99m-sestamibi myocardial scintigraphy and mitochondrial cytochrome oxidase activity in hypertrophic cardiomyopathy
- CLINICAL INVESTIGATION INTO THE MECHANISMS OF PULMONARY CONGESTION IN ACUTE MYOCARDIAL INFARCTION : Ischemic Heart Disease (III) : III : 48 Annual Scientific Meeting, Japanese Circulation Society
- Usefulness of Acoustic Densitometry Method for Detection of Myocardial Changes in Preclinical Patients with Hypertrophic Cardiomyopathy
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