Mabuchi Tomohito | Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O

スポンサーリンク

概要

関連著者

もっと見る

著作論文

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
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-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
Plasma Endothelin-1 Elevation Associated With Alcohol-Induced Variant Angina
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

もっと見る

スポンサーリンク