Pages that link to "Q37613089"

The following pages link to Genotype- and phenotype-guided management of congenital long QT syndrome (Q37613089):

Displaying 40 items.

• Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery (Q26744730) (← links)
• Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison (Q26772794) (← links)
• Sodium channel β subunits: emerging targets in channelopathies (Q28082122) (← links)
• Identification and Functional Characterization of a Novel CACNA1C-Mediated Cardiac Disorder Characterized by Prolonged QT Intervals With Hypertrophic Cardiomyopathy, Congenital Heart Defects, and Sudden Cardiac Death (Q29347533) (← links)
• Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside. (Q30378666) (← links)
• Phenotype guided characterization and molecular analysis of Indian patients with long QT syndromes. (Q33167556) (← links)
• Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long QT Syndrome (Q33168257) (← links)
• KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1. (Q33886242) (← links)
• Genetic analysis, in silico prediction, and family segregation in long QT syndrome (Q34705080) (← links)
• Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing (Q35232613) (← links)
• Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel (Q37002974) (← links)
• Early somatic mosaicism is a rare cause of long-QT syndrome (Q37346748) (← links)
• Cardiac disease modeling using induced pluripotent stem cell-derived human cardiomyocytes (Q38393181) (← links)
• Congenital Long QT syndrome and torsade de pointes. (Q38663670) (← links)
• Molecular Pathophysiology of Congenital Long QT Syndrome (Q38997049) (← links)
• Evaluation of Prolonged QT Interval: Structural Heart Disease Mimicking Long QT Syndrome (Q39117176) (← links)
• Precision Cardiovascular Medicine: State of Genetic Testing. (Q39224845) (← links)
• Electrocardiographic intervals associated with incident atrial fibrillation: Dissecting the QT interval. (Q40339412) (← links)
• Sudden infant death syndrome, sleep, and seizures (Q41707715) (← links)
• Clinical Genetic Testing for the Cardiomyopathies and Arrhythmias: A Systematic Framework for Establishing Clinical Validity and Addressing Genotypic and Phenotypic Heterogeneity (Q41936884) (← links)
• Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report (Q42070270) (← links)
• Computational Cardiac Modeling Reveals Mechanisms of Ventricular Arrhythmogenesis in Long QT Syndrome Type 8: CACNA1C R858H Mutation Linked to Ventricular Fibrillation (Q42372853) (← links)
• Strain Echocardiography and LQTS Subtypes: Mechanical Alterations in an Electrical Disorder (Q42426904) (← links)
• Ventricular fibrillation after elective surgery in an adolescent with long QT syndrome (Q44427266) (← links)
• Drug-Mediated Shortening of Action Potentials in LQTS2 Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes (Q47141643) (← links)
• Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A. (Q47150598) (← links)
• Mechanisms and models of cardiac sodium channel inactivation. (Q47758712) (← links)
• Is Symptomatic Long QT Syndrome Associated with Depression in Women and Men? (Q48044319) (← links)
• Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing. (Q50066417) (← links)
• The genetic architecture of long QT syndrome: A critical reappraisal (Q52584821) (← links)
• A Potential Diagnostic Approach for Foetal Long-QT Syndrome, Developed and Validated in Children (Q57144746) (← links)
• Long QT Syndrome Modelling with Cardiomyocytes Derived from Human-induced Pluripotent Stem Cells (Q64074244) (← links)
• Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant. (Q64985307) (← links)
• Calcium Revisited: New Insights Into the Molecular Basis of Long-QT Syndrome (Q87846139) (← links)
• Genetics and pharmacogenetics in the diagnosis and therapy of cardiovascular diseases (Q90435012) (← links)
• Cardiac conduction defects (Q90435018) (← links)
• Cardiovascular Precision Medicine in the Genomics Era (Q90652947) (← links)
• Practical Aspects in Genetic Testing for Cardiomyopathies and Channelopathies (Q92133261) (← links)
• Phenotype-Based High-Throughput Classification of Long QT Syndrome Subtypes Using Human Induced Pluripotent Stem Cells (Q92396903) (← links)
• The Functional Role of Voltage-Gated Sodium Channel Nav1.5 in Metastatic Breast Cancer (Q98464897) (← links)