Hayashi Tatsumi | Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Kanazawa Universi

スポンサーリンク

概要

関連著者

もっと見る

著作論文

PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
PE-067 Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Hypertrophic Cardiomyopathy Caused by Cardiac Troponinl Gene Mutation(Cardiomyopathy, basic/clinical-3 (M) PE12,Poster Session (English),The 70th Anniversary Annual Scientific Meeting
OJ-223 A Novel Missense Mutation Met1107Thr in Cardiac Ryanodine Receptor Gene is Associated with Hypertrophic Cardiomyopathy(Cardiomyopathy, basic/clinical-2 (M) OJ38,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japa
OE-284 Usefulness of Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Patients with Hypertrophic Cardiomyopathy Associated with TNNI3 Gene Mutation(MRI/MRA-1 (I) OE48,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeti
OE-265 Genotype-Phenotype Variations in Cardiomyopathies Caused by a Cardiac Troponin I Gene Mutation(Cardiomyopathy, basic/clinical-1 (M) OE45,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
OE-088 Differences in Diagnostic Value of Various Criteria of Negative T Waves for Hypertrophic Cardiomyopathy in a Genotyped Population(ECG/Body surface potential mapping/Holter-1 (A) OE15,Oral Presentation (English),The 70th Anniversary Annual Scientifi
FRS-104 Association between Angiotensin II Receptor Gene Polymorphism and Left Ventricular Systolic Dysfunction in Sarcomere Gene Mutation-induced Hypertrophic Cardiomyopathy(Frontier of Cardiomyopathy Research-2 (M) FRS21,Featured Research Session (Engli
In-hospital Outcome in Octogenarians with Acute Coronary Syndrome Undergoing Emergent Coronary Angiography
FRS-128 Mutations in Phospholamban Gene Cause Hypertrophic and Dilated Cardiomyopathy(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
Relationship between QT Variables and Disproportion of Left Ventricular Wall in Patients with Hypertrophic Cardiomyopathy
Fluctuation of T-peak to T-end before and after ventricular tachycardia
Q-T peak dispersion in congenital long QT syndrome ; increased lag of T wave peak as a new marker of HERG
Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome
Q-T peak dispersion in congenital long QT syndrome: Possible marker of mutation of HERG
Cardiac Manifestations and Long-Term Course in Emery-Dreifuss Muscular Dystrophy Caused by a Nonsense Mutation in the STA Gene
Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome
A novel de novo mutation in the cardiac β - myosin heavy chain gene in patients with dilated cardiomyopathy
Mitochondrial DNA mutations in hypertrophic cardiomyopathy
Novel KCNQ1 missense mutation (D611Y) in a Japanese long QT family
Whole and regional variation of cardiac sympathetic nervous activity in patients with hypertrophic cardiomyopathy with malignant tachyarrthythmias and sudden death
Spontaneous Development of Left Ventricular Aneurysm in a Patient With Untreated Cardiac Sarcoidosis
Cardiac papillary fibroelastoma originated from atrial side of mitral valve leaflet

もっと見る

スポンサーリンク