Mabuchi Tomohito | Department of Cardiology, Fukui Prefectural Hospital

スポンサーリンク

概要

関連著者

もっと見る

著作論文

PJ-540 Risk of Surgery after Coronary Drug-Eluting Stent Implantation(PJ091,Coronary Revascularization, PCI (DES) 3 (IHD),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
Gene mutations in adult Japanese patients with dilated cardiomyopathy
Coronary lesion morphology and prognosis in young males with myocardial infarction with or without familial hypercholesterolemia
Diagnostic usefulness of the post-exercise systolic blood pressure response for the detection of coronary artery disease in patients with diabetes mellitus
Distribution of QTc Values and Prevalence of Short QT Syndrome in the Japanese Population (ECG/Body Surface Potential Mapping/Holter 6 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Gene Mutations in Patients with Hypertrophic Cardiomyopathy Showing Mild Left Ventricular Hypertrophy(Cardiomyopathy, Clinical 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Differences in Diagnostic Value of Classic Electrocardiographic Voltage Criteria for Hypertrophic Cardiomyopathy in a Genotyped Population(Cardiomyopathy, Clinical 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Ankyrin-B Gene Mutation is a Rare Cause of Long QT Syndrome in Japan(Arrhythmia, Basic 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Long-Term Course of Patients with Cardiomyopathy Associated with Phospholamban Gene Mutations(Cardiomyopathy, Clinical 8 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Early Development of Dilated Cardiomyopathy in Subjects with Hypertrophic Cardiomyopathy Caused by Mutations of the Thin Filament Genes(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Angiotensin II Type 1 Receptor A/C1166 Gene Polymorphism and Left Ventricular Systolic Dysfunction in Hypertrophic Cardiomyopathy with Sarcomere Gene Mutations(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation
Impact of Bundle-Branch Block on Clinical Manifestation in Patients with Hypertrophic Cardiomyopathy : Analyses Based on Molecular Genetic Diagnoses(Cardiomyopathy, Clinical 6 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
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
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)
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-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
Left ventricular dysfunction and dilatation in elderly patients with hypertrophic cardiomyopathy associated with a novel missense mutation in MyBP-C gene
Probucol-Induced Long QT Syndrome Associated with a Novel Missense Mutation M124T in the N Terminus of HERG
Long QT Syndrome Mutations in Different Sites of HERG Elicit a Variety of Functional Changes
Double Missense Mutations (D611Y in KCNQ1 and D609G in HERG) in a Japanese Family with Long QT Syndrome
IS130 Dipylidamole induced stunning continues for at least one hour in patients with coronary artery disease : Evaluation with quantitative gated SPECT
Usefulness of Acoustic Densitometry Method for Detection of Myocardial Changes in Preclinical Patients with Hypertrophic Cardiomyopathy
Association between Single Nucleotide Polymorphisms (SNPs) of Cardiac Potassium Channel Genes and Drug-Induced Long QT Syndrome in Japanese
A Novel Mutation (lnt21DSG+1A) in the MyBP-C Gene Shows Hypertrophic Cardiomyopathy with a High Degree of Penetrance in Adult Patients
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
Differences in Diagnostic Values of Abnormal Q Waves between Hypertrophic Cardiomyopathy with a cTnl Gene Mutation and MyBP-C Gene Mutations
Emergent thoracic aortic angioplasty and stenting for middle aortic syndrome in non-specific aortitis

もっと見る

スポンサーリンク