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102. A Common Mutation of Long QT Syndrome Type 1 in Japan

103. A type 2 ryanodine receptor variant associated with reduced Ca2+ release and short-coupled torsades de pointes ventricular arrhythmia.

110. A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels

118. Identification of a KCNQ1 Polymorphism Acting as a Protective Modifier Against Arrhythmic Risk in Long-QT Syndrome

121. Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

123. Phenotype Variability in Patients Carrying KCNJ2 Mutations

125. 290 The KCNQ1 rs2074238 polymorphism is a genetic modifier of cardiac risk in long QT syndrome

128. Clinical and electrocardiographic characteristics of patients with short QT interval in a large hospital-based population

129. Seasonal and Circadian Distributions of Cardiac Events in Genotyped Patients With Congenital Long QT Syndrome

131. KCNE5 ( KCNE1L ) Variants Are Novel Modulators of Brugada Syndrome and Idiopathic Ventricular Fibrillation

134. Intrathecally administered Sema3A protein attenuates neuropathic pain behavior in rats with chronic constriction injury of the sciatic nerve

136. Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia

138. Long QT syndrome with compound mutations is associated with a more severe phenotype: A Japanese multicenter study

139. Atrioventricular Block-Induced Torsades de Pointes With Clinical and Molecular Backgrounds Similar to Congenital Long QT Syndrome

140. Japanese Journal of Electrocardiology

141. Japanese Journal of Electrocardiology

144. Aortopulmonary Artery Dissection

145. Latent Genetic Backgrounds and Molecular Pathogenesis in Drug-Induced Long-QT Syndrome

146. D85N, a KCNE1 Polymorphism, Is a Disease-Causing Gene Variant in Long QT Syndrome

148. Dynamic Change in ST-Segment and Spontaneous Occurrence of Ventricular Fibrillation in Brugada Syndrome With a Novel Nonsense Mutation in the SCN5A Gene During Long-Term Follow-up

150. Hydroxyzine, a First Generation H1-Receptor Antagonist, Inhibits Human Ether-a-go-go–Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation

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