Novel insight into the natural history of short QT syndrome. - Wikidata - wikimedia - TriplyDB

Novel insight into the natural history of short QT syndrome.

Novel insight into the natural history of short QT syndrome.

http://www.wikidata.org/entity/Q37706496

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Next-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death Cases Genetics of channelopathies associated with sudden cardiac death Genetics of inherited primary arrhythmia disorders 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the The new kids on the block of arrhythmogenic disorders: Short QT Syndrome and early repolarization.[Primary and secondary prophylactic ICD therapy in congenital electrical and structural cardiomyopathies].Sinus bradycardia, junctional rhythm, and low-rate atrial fibrillation in Short QT syndrome during 20 years of follow-up: three faces of the same genetic problem.The prevalence and significance of a short QT interval in 18,825 low-risk individuals including athletes.Short QT Syndrome - Review of Diagnosis and Treatment.Short QT syndrome in pediatrics.Long-Term Outcome of Patients With Idiopathic Ventricular Fibrillation: A Meta-Analysis.Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2.Hydrocinnamic Acid Inhibits the Currents of WT and SQT3 Syndrome-Related Mutants of Kir2.1 Channel.Drug-Induced QT/QTc Interval Shortening: Lessons from Drug-Induced QT/QTc Prolongation.Is There a Role for Genetics in the Prevention of Sudden Cardiac Death?Avoiding sports-related sudden cardiac death in children with congenital channelopathy : Recommendations for sports activities.Styrax blocks inward and outward current of Kir2.1 channel.Sudden cardiac death: focus on the genetics of channelopathies and cardiomyopathies.In silico investigation of a KCNQ1 mutation associated with short QT syndrome.The Pharmacogenomics of a Mutation 'Hotspot' for the Short QT Syndrome.Clinical Genetic Testing for the Cardiomyopathies and Arrhythmias: A Systematic Framework for Establishing Clinical Validity and Addressing Genotypic and Phenotypic Heterogeneity.Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.Repolarization characteristics in early repolarization and brugada syndromes: insight into an overlapping mechanism of lethal arrhythmias.Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome.Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death.Athletes with channelopathy may be eligible to play.Modeling Short QT Syndrome Using Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes.Ion Channel Disorders and Sudden Cardiac Death.Primary Ventricular Fibrillation in a Patient with Mild Hypercalcemia.Issues in the management of invasive pulmonary aspergillosis in non-neutropenic patients in the intensive care unit: A role for isavuconazole.Recent Advances in Short QT Syndrome Mutations in voltage-gated L-type calcium channel: implications in cardiac arrhythmia

P2860

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P2860

Novel insight into the natural history of short QT syndrome.

http://www.wikidata.org/entity/Q37706496

description

2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh

2013年學術文章

@zh-hant

name

Novel insight into the natural history of short QT syndrome.

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Novel insight into the natural history of short QT syndrome.

@nl

type

label

Novel insight into the natural history of short QT syndrome.

@en

Novel insight into the natural history of short QT syndrome.

@nl

prefLabel

Novel insight into the natural history of short QT syndrome.

@en

Novel insight into the natural history of short QT syndrome.

@nl

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Journal of the American College of Cardiology

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Novel insight into the natural history of short QT syndrome

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Agnieszka Zienciuk-Krajka

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Ajita Kanthan

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Andreea Elena Surducan

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Antonio Curcio

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Carlotta Miceli

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Gianluca Borio

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Mario Colombo

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Mirella Memmi

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Nicola Monteforte

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Raffaella Bloise

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P2860

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)

Natural history of Brugada syndrome: insights for risk stratification and management.

Short QT Syndrome: a familial cause of sudden death.

Short QT syndrome: clinical findings and diagnostic-therapeutic implications.

The short QT syndrome: proposed diagnostic criteria.

Long-term follow-up of patients with short QT syndrome.

Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry.

Long-term follow-up of a pediatric cohort with short QT syndrome.

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13

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Valeria Novelli

Carlo Napolitano

Andrea Mazzanti

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2013-11-28T00:00:00Z

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259108570

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