Ueda Kazuo | Department Of Internal Medicine Kyorinkai Murakami Memorial Hospital

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著作論文

PJ-574 A Novel Missense Mutation (R2401H) in the Human Cardiac Ryanodine Receptor Gene (RyR2) in Patient with Catecholaminergic Polymorphic Ventricular Tachycardia(Arrhythmia, Basic and Diagnosis/Pathophysiology/EPS (A) : PJ96)(Poster Session (Japanese))
Infrared Study of Surface Phonon Modes in ZnO Small Crystals
OJ-504 Functional alterations of TCAP mutations found in hypertrophic cardiomyopathy and dilated cardiomyopathy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
OJ-083 KCNQ1 Mutation Causing Defective Channel Trafficking and Dominant-Negative Suppression Underlie Severe Phenotype of Congenital Long QT Syndrome(Arrhythmia, Basic 1 (A) : OJ10)(Oral Presentation (Japanese))
Eigenstates in 2-Dimensional Penrose Tiling
Some Remarks on Anomalous Distribution of Internal Fields in Al_4Mn Quasicrystals
Identification of English /r/ and /l/ in noise : The effects of baseline performance
Mutational Analysis of Cardiac Ryanodine Receptor Genes (RyR2) in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Arrhythmogenic Right Ventricular Cardiomyopathy(Arrhythmia, Basic 2 (A), The 69th Annual Scientific Meeting of the Ja
FRS-026 HERG potassium channel regulated by phosphotyrosine kinase(Arrhythmia-Basic : Molecular and Genetic : Basis (A) : FRS4)(Featured Research Session (English))
What factors accelerate aortic stiffening in hemodialysis patients? An observational study
Effects of Glucose Metabolism on Aortic Pulse Wave Velocity in Hemodialysis Patients with and without Diabetes
Determinants of Arterial Wall Stiffness and Peripheral Artery Occlusive Disease in Nondiabetic Hemodialysis Patients
A Novel Frameshift Mutation in C-Terminal Region of HERG
A Novel Disease Genes for Cardiomyopathy : Identification of a CAV3 Mutation and Its Functional Alteration
Novel HERG mutations in long QT syndrome in Japan
Genetic risk factors for myocardial infarction in Japanese
Identification of caveolin-3 mutation in familial cardiomyopathy
Mutation of ZASP causes alteration in the affinity to protein kinase C subtypes and associates with familial dilated cardiomyopathy
An Autopsy Case of Idiopathic Myocardial Hypertrophy, the Heart Weight of which indicated 1,000 gr
Does filled duration illusion occur for very short time intervals?
Short-term auditory memory interference : The Deutsch demonstration revisited
Perceptual Organization of Onsets and Offsets of Sounds
An Artificial Environment is Often a Noisy Environment : Auditory Scene Analysis and Speech Perception in Noise
Technical Listening Training : Improvement of sound sensitivity for acoustic engineers and sound designers

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