477 results on '"Konno, Tetsuo"'
Search Results
102. High Sensitivity of Late Gadolinium Enhancement for Predicting Microscopic Myocardial Scarring in Biopsied Specimens in Hypertrophic Cardiomyopathy
103. Impact of combined lipid lowering with blood pressure control on coronary plaque regression: rationale and design of MILLION study
104. VULNERABLE CORONARY PLAQUES STILL EXIST EVEN IN LOW LDL-C LEVELS: EVIDENCE FROM STUDY WITH SERIAL CT CORONARY ANGIOGRAPHY
105. Impact of Fluoroscopically-Visible Fluttering Flap on Clinical Diagnosis of Acute Aortic Dissection
106. FRAGMENTED QRS PREDICTS CARDIAC EVENTS IN HYPERTROPHIC CARDIOMYOPATHY
107. Erdheim-Chester Disease Involving the Brain and the Heart
108. Relationships between Alanine Aminotransferase(ALT), Visceral Adipose Tissue(AT) and Metabolic Risk Factors in a Middle-Aged Japanese Population
109. Can Next-Generation Sequencing Replace Sanger Sequencing for Screening Genetic Variants?
110. Fragmented QRS Predicts Heart Failure Progression in Patients With Hypertrophic Cardiomyopathy
111. Abstract 9314: Clinical Impact of Heterozygous Carrier of ATP-binding Cassette Sub-family G Member 5 Gene on Asymptomatic Normolipidemic Patients: Evidence From Familial Gene Analysis
112. Abstract 9313: Progression of Coronary Plaque Burden In Patients With Familial Hypercholesterolaemia: Assessment With Coronary CT
113. Impact of lesion morphology and associated procedures for left main coronary stenting on angiographic outcome after intervention: sub-analysis of Heart Research Group of Kanazawa, HERZ, Study
114. Efficacy of Aliskiren for Patients with Hypertension Receiving Angiotensin-Converting Enzyme Inhibitors and/or Angiotensin-Receptor Blockers
115. Current perspectives in genetic cardiovascular disorders: from basic to clinical aspects
116. Platypnea-Orthodeoxia Syndrome
117. Is exercise-related QT interval shortening with a peaked T wave a specific electrocardiographic finding of pheochromocytoma?
118. IMPACT OF RIGHT VENTRICULAR HYPERTROPHY ON SEVERE CLINICAL PHENOTYPES IN HYPERTROPHIC CARDIOMYOPATHY: EVIDENCE FROM MRI
119. A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome
120. Polymorphic ventricular tachycardia in a patient with hypertrophic cardiomyopathy and digitalis intoxication
121. Anomalous Origin With Myocardial Bridging in Coronary Artery
122. Impact of Systolic Dysfunction in Genotyped Hypertrophic Cardiomyopathy
123. Stress-induced takotsubo cardiomyopathy complicated with wall rupture and thrombus formation
124. Age at the Onset of Hypertrophy in the Genotyped Hypertrophic Cardiomyopathy
125. Impact of out-stent plaque volume on in-stent intimal hyperplasia: Results from serial volumetric analysis with high-gain intravascular ultrasound
126. Immediate disappearance of large thrombus in left atrium without evidence of systemic embolization after heparin treatment
127. Perfect Correspondence of Mitral Valve Perforation Using Real-Time 3-Dimensional Transesophageal Echocardiography
128. IMPACT OF PITAVASTATIN PRETREATMENT ON SURVIVAL AND FUNCTIONAL ACTIVITIES OF MESENCHYMAL STEM CELL: POSSIBLE IMPLICATION FOR CELL TRANSPLANTATION THERAPY
129. IMPACT OF POTASSIUM CHANNEL GENE MUTATIONS ON OCCURRENCE OF LONE ATRIAL FIBRILLATION
130. Pulmonary hypertension associated with veno-occlusive disease in systemic sclerosis: Insight into the mechanism of resistance to vasodilator
131. Altered Metabolism of Low-Density Lipoprotein and Very-Low-Density Lipoprotein Remnant in Autosomal Recessive Hypercholesterolemia
132. Expression and Function of Ephrin-B1 and Its Cognate Receptor EphB2 in Human Abdominal Aortic Aneurysm
133. A novel type of familial hypercholesterolemia: Double heterozygous mutations in LDL receptor and LDL receptor adaptor protein 1 gene
134. Abstract 8252: Altered Metabolism of Post-Prandial Remnant Lipoprotein Fractions in Autosomal Recessive Hypercholesterolemia
135. Abstract 9712: Lack of Association Between Common p.T111I Variant in the Endothelial Lipase Gene and the Risk for Coronary Artery Disease in Familial Hypercholesterolemia: Insights From the Modulation of Phospholipids in the HDL Particles
136. Abstract 8511: A Novel Type of Homozygous Familial Hypercholesterolemia:Double Heterozygous Mutations in LDL Receptor and LDL Receptor Adaptor Protein 1 Gene
137. Rapid progression of coronary artery disease in a patient with retroperitoneal fibrosis
138. Impact of Bilateral Internal Thoracic-to-Epigastric Artery Communications on Salvaging Total Lower Limb Ischemia
139. IMPACT OF OUT-STENT PLAQUE VOLUME ON IN-STENT INTIMAL HYPERPLASIA: RESULTS FROM SERIAL VOLUMETRIC ANALYSIS WITH HIGH-GAIN INTRAVASCULAR ULTRASOUND
140. THE IMPACT OF SYSTOLIC DYSFUNCTION ON PROGNOSIS OF GENOTYPED HYPERTROPHIC CARDIOMYOPATHY
141. CHARACTERIZATION OF COMPOUND HETEROZYGOSITY FOR MUTATIONS R269W IN KCNH2 AND P1824A IN SCN5A ASSOCIATED WITH LONG QT SYNDROME AND SINUS NODE DYSFUNCTION
142. Impact of reduced left atrial functions on diagnosis of paroxysmal atrial fibrillation: Results from analysis of time-left atrial volume curve determined by two-dimensional speckle tracking
143. Gene and Protein Expression Analysis of Mesenchymal Stem Cells Derived From Rat Adipose Tissue and Bone Marrow
144. Systolic Dysfunction and Prognosis in Genotyped Hypertrophic Cardiomyopathy
145. Prevention of Ventricular Arrhythmia and Calcium Dysregulation in a Catecholaminergic Polymorphic Ventricular Tachycardia Mouse Model Carrying Calsequestrin-2 Mutation
146. Genetics of hypertrophic cardiomyopathy
147. Impact of inflow reduction of arteriovenous fistula on systemic hemodynamics in a patient with high-output heart failure during hemodialysis: A case report
148. INHIBITION OF CARDIAC FIBROSIS MEDIATED BY NON-MYOCYTE PROLIFERATION IN HYPERTROPHIC CARDIOMYOPATHY
149. Low Electrocardiogram Voltage due to Anasarca
150. Late Onset of Cholesterol Crystal Embolism after Thrombolysis for Cerebral Infarction
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