Unexplained drownings and the cardiac channelopathies: a molecular autopsy series. - Wikidata - awgldk - TriplyDB

Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

http://www.wikidata.org/entity/Q35248041

about

Inherited arrhythmias: The cardiac channelopathies Unintentional drowning: Role of medicinal drugs and alcohol 'Autonomic conflict': a different way to die during cold water immersion?Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation Ryanodine receptor mutations presenting as idiopathic ventricular fibrillation: a report on two novel familial compound mutations, c.6224T>C and c.13781A>G, with the clinical presentation of idiopathic ventricular fibrillation.Citalopram-Induced Long QT Syndrome and the Mammalian Dive Reflex.The role of hereditary KCNQ1 mutations in water-related death.The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths.Autonomic conflict exacerbates long QT associated ventricular arrhythmia.Ictal Mammalian Dive Response: A Likely Cause of Sudden Unexpected Death in Epilepsy

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Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

http://www.wikidata.org/entity/Q35248041

description

2011 nî lūn-bûn

@nan

2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

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Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

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type

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Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

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Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

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prefLabel

Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

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Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

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Mayo Clinic Proceedings

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Unexplained drownings and the cardiac channelopathies: a molecular autopsy series

@en

P2093

David J Tester

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Melissa L Will

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Michael J Ackerman

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P2860

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading fram

Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

Pathogenesis of unexplained drowning: new insights from a molecular autopsy.

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941-947

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scholarly article

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10.4065/MCP.2011.0373

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10

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Argelia Medeiros-domingo

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51686237

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3184023

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