Hiroshi Mabuchi


Ontology type: schema:Person     


Person Info

NAME

Hiroshi

SURNAME

Mabuchi

Publications in SciGraph latest 50 shown

  • 2016-04-02 Changes in lipoprotein lipase and endothelial lipase mass in familial hypercholesterolemia during three-drug lipid-lowering combination therapy in LIPIDS IN HEALTH AND DISEASE
  • 2015-03-13 Extreme Contrast of Postprandial Remnant-Like Particles Formed in Abetalipoproteinemia and Homozygous Familial Hypobetalipoproteinemia in JIMD REPORTS, VOLUME 22
  • 2015-02-10 Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by Breastfeeding in JIMD REPORTS, VOLUME 21
  • 2014-11-18 PCSK9 inhibitors for treating familial hypercholesterolaemia in NATURE REVIEWS ENDOCRINOLOGY
  • 2010-11-25 Comparison of the effects of losartan vs. ramipril on several adipocytokines and vascular remodeling biomarkers in HYPERTENSION RESEARCH
  • 2010-10-29 A possible new syndrome with double endocrine tumors in association with an unprecedented type of familial heart-hand syndrome: a case report in JOURNAL OF MEDICAL CASE REPORTS
  • 2010-02-03 Human Cholesteryl Ester Transfer Protein in Human HDL Metabolism in HIGH DENSITY LIPOPROTEINS, DYSLIPIDEMIA, AND CORONARY HEART DISEASE
  • 2007-12 Telmisartan Treatment Decreases Visceral Fat Accumulation and Improves Serum Levels of Adiponectin and Vascular Inflammation Markers in Japanese Hypertensive Patients in HYPERTENSION RESEARCH
  • 2007-10-24 Comparison of Effects of Pitavastatin and Atorvastatin on Plasma Coenzyme Q10 in Heterozygous Familial Hypercholesterolemia: Results From a Crossover Study in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2007-02 Effects of Hypertension and Type 2 Diabetes Mellitus on the Risk of Total Cardiovascular Events in Japanese Patients with Hypercholesterolemia: Implications from the Japan Lipid Intervention Trial (J-LIT) in HYPERTENSION RESEARCH
  • 2006 High‐HDL Syndrome in ENCYCLOPEDIC REFERENCE OF GENOMICS AND PROTEOMICS IN MOLECULAR MEDICINE
  • 2006-01 Pathophysiological Roles of the Adrenal Renin-Angiotensin System in Patients with Primary Aldosteronism in HYPERTENSION RESEARCH
  • 2005-11 The Risk of Cardiovascular Events in Japanese Hypertensive Patients with Hypercholesterolemia: Sub-Analysis of the Japan Lipid Intervention Trial (J-LIT) Study, a Large-Scale Observational Cohort Study in HYPERTENSION RESEARCH
  • 2005-07 Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy in ANNALS OF NUCLEAR MEDICINE
  • 2005-07 Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction in ANNALS OF NUCLEAR MEDICINE
  • 2005-05-01 Risk of Colorectal Neoplasm in Patients with Acromegaly and its Relationship with Serum Growth Hormone Levels in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2004-11 Association between CTLA-4 +49 A/G polymorphism and type 1B diabetes in Japanese population in ENDOCRINE
  • 2003-07-01 Up-Regulation of cyr61 in Vascular Smooth Muscle Cells of Spontaneously Hypertensive Rats in LABORATORY INVESTIGATION
  • 2003-05 Cardiac sympathetic nerve activity in patients with hypertrophic cardiomyopathy with malignant ventricular tachyarrhythmias in JOURNAL OF NUCLEAR CARDIOLOGY
  • 2003-03-26 Haplotype analyses of cholesteryl ester transfer protein gene promoter: a clue to an unsolved mystery of TaqIB polymorphism in JOURNAL OF MOLECULAR MEDICINE
  • 2002-06 Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease in JOURNAL OF HUMAN GENETICS
  • 2002-02 Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III in JOURNAL OF HUMAN GENETICS
  • 2001-11-01 Iron accumulation in the liver of male patients with Wilson's disease in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2001-04 Effects of hepatic lipase gene promoter nucleotide variations on serum HDL cholesterol concentration in the general Japanese population in JOURNAL OF HUMAN GENETICS
  • 2000-09 New treatment for eradication of Helicobacter pylori: effective and inexpensive combination in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2000-04 A new variant deletion of a copper-transporting P-type ATPase gene found in patients with Wilson's disease presenting with fulminant hepatic failure in JOURNAL OF GASTROENTEROLOGY
  • 2000 Common Mutation of 5, 10-Methylenetetrahydrofolate Reductase Accelerates Coronary Artery Disease in Familial Hypercholesterolemia in LIPOPROTEIN METABOLISM AND ATHEROGENESIS
  • 2000 Molecular Genetics and Clinical Features of Japanese Patients with Familial Hypercholesterolemia in LIPOPROTEIN METABOLISM AND ATHEROGENESIS
  • 1998-11-01 Detection of diaphragmatic defect as the cause of severe hepatic hydrothorax with magnetic resonance imaging in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 1996 Molecular Genetics of Cholesterol Transport and Cholesterol Reverse Transport Disorders, and Coronary Heart Disease in DRUGS AFFECTING LIPID METABOLISM
  • 1993-03 Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by an intron 14 splicing defect in hyperalphalipoproteinemia in HUMAN GENETICS
  • 1990 Development of coronary heart disease in familial hypercholesterolemia in ATHEROSCLEROSIS AND CARDIOVASCULAR DISEASE
  • 1989-11-01 Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins in NATURE
  • 1987 Long-Term Effects of CS-514 on Serum Lipoprotein Lipid and Apolipoprotein Levels in Patients with Familial Hypercholesterolemia in DRUGS AFFECTING LIPID METABOLISM
  • 1982-09 Pseudohomozygous type II hyperlipoproteinemia in JOURNAL OF HUMAN GENETICS
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