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Kanazawa Univ. School Of Medicine Kanazawa Jpn | 論文
- 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
- PJ-515 Plasma Reduced form of Antioxidant Coenzyme Q10 (Ubiquinol-10) is Associated with Oxidized LDL in Heterozygous Familial Hypercholesterolemia(Lipid disorders-3, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Clinical Efficacy and Safety of Rosuvastatin in Japanese Patients With Heterozygous Familial Hypercholesterolemia
- Occupational Exposure to Low Concentrations of Organic Solvents in Shipyards
- Prevention of a Malaria Outbreak among Non-Immune Japanese Workers Engaged in the Construction of a Thermal Power Plant in Sonebhadra, India
- Difference in the risk factors for coronary, renal and other peripheral arteriosclerosis in heterozygous familial hypercholesterolemia
- Retinoid X Receptor Heterodimer Variants and Cardiovascular Risk Factors
- PE-252 Common Variant of Farnesoid-X-receptor Gene Enhances the Response to Lipid-Lowering Therapy(Lipid disorders-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- The Relationship of Percent Body Fat by Bioelectrical Impedance Analysis with Blood Pressure, and Glucose and Lipid Parameters
- Association of Genetic Variation of the Adiponectin gene with Body Fat Distribution and Carotid Atherosclerosis in Japanese Obese Subjects
- Increased Circulating Matrix Metalloproteinase-2 in Patients with Hypertrophic Cardiomyopathy with Systolic Dysfunction
- Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
- 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)
- 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)
- 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)
- Significance of Decreased Plasma D-Dimer Levels following Lipopolysaccharide-Induced Disseminated Intravascular Coagulation in Rats
- Adult-Onset Still's Disease with Submassive Hepatic Necrosis
- Analysis of COL8A2 Gene Mutation in Japanese Patients with Fuchs' Endothelial Dystrophy and Posterior Polymorphous Dystrophy
- Mutation Analysis of the PTEN/MMAC1 Gene in Japanese Patients with Cowden Disease
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