Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals - Wikidata - wikimedia - TriplyDB

Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals

Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals

http://www.wikidata.org/entity/Q35904744

about

A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation Genetics of inherited primary arrhythmia disorders Long-QT syndrome: from genetics to management Rationale and objectives for ECG screening in infancy Molecular pathogenesis of long QT syndrome type 1 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 Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications.Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy.Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome.Sudden cardiac arrest during sex in patients with either catecholaminergic polymorphic ventricular tachycardia or long-QT syndrome: a rare but shocking experience.Long-QT Syndrome and Therapy for Attention Deficit/Hyperactivity Disorder.Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGs [Indications for implantable loop recorders in patients with channelopathies and ventricular tachycardias].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.Hyperglycemia is associated with corrected QT prolongation and mortality in acutely ill patients.Genetics of sudden cardiac death.Perceptions of an implantable cardioverter-defibrillator: A qualitative study of families with a history of sudden life-threatening cardiac events and recommendations to improve care.Inherited arrhythmia syndromes leading to sudden cardiac death in the young: a global update and an Indian perspective.AKAP9 is a genetic modifier of congenital long-QT syndrome type 1 Sports Participation in Genotype Positive Children With Long QT Syndrome.Genotype- and Sex-Specific QT-RR Relationship in the Type-1 Long-QT Syndrome.Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl."QT clock" to improve detection of QT prolongation in long QT syndrome patients.Clinical and genetic features of Australian families with long QT syndrome: A registry-based study.Interpreting secondary cardiac disease variants in an exome cohort.Genotype- and phenotype-guided management of congenital long QT syndrome.Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort Racial susceptibility for QT prolongation in acute drug overdoses.Congenital long and short QT syndromes.The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy.Genetic etiology and evaluation of sudden cardiac death.Genetic testing for inherited cardiac disease.The measurement of the QT interval.Must every child with long QT syndrome take a beta blocker?Congenital long QT syndromes: prevalence, pathophysiology and management.Triggering of cardiac arrhythmic events in long QT syndrome: lessons from funny bunnies.Allelic Complexity in Long QT Syndrome: A Family-Case Study.QTc interval in patients with schizophrenia receiving antipsychotic treatment as monotherapy or polypharmacy.Revealing the Concealed Nature of Long-QT Type 3 Syndrome.

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Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals

http://www.wikidata.org/entity/Q35904744

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2011年论文

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Risk for life-threatening card ...... l-range corrected QT intervals

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Risk for life-threatening card ...... l-range corrected QT intervals

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J.JACC.2010.07.038

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Journal of the American College of Cardiology

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Risk for life-threatening card ...... l-range corrected QT intervals

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Alon Barsheshet

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Arthur J Moss

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Coeli M Lopes

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Elizabeth S Kaufman

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Emanuela H Locati

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G Michael Vincent

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Ilan Goldenberg

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Jennifer L Robinson

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Jesaia Benhorin

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Li Zhang

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P2860

Risk stratification in the long-QT syndrome.

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome.

Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome.

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.

Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome.

Risk of death in the long QT syndrome when a sibling has died.

The long QT syndrome. Prospective longitudinal study of 328 families.

QTc: how long is too long?

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

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1

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Peter J. Schwartz

Carlo Napolitano

Wojciech Zareba

Jeffrey A Towbin

Arthur A M Wilde

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2011-01-01T00:00:00Z

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49709081

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