The molecular autopsy: should the evaluation continue after the funeral? (Q26864392)

Michael J. Ackerman

series ordinal

2

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language of work or name

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March 2012

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33

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issue

3

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page(s)

461-70

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The sudden infant death syndrome

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Sodium channel mutations and arrhythmias

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Postmortem molecular screening for cardiac ryanodine receptor type 2 mutations in sudden unexplained death: R420W mutated case with characteristics of status thymico-lymphatics

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Identification of novel missense mutations of cardiac ryanodine receptor gene in exercise-induced sudden death at autopsy

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Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing

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Sudden cardiac death without structural heart disease: update on the long QT and Brugada syndromes

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Cardiac causes of sudden unexpected death in children and their relationship to seizures and syncope: genetic testing for cardiac electropathies

28 September 2017

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Sudden adult death syndrome and other non-ischaemic causes of sudden cardiac death

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Sudden death in patients without structural heart disease

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A Missense Mutation in the CASQ2 Gene Is Associated with Autosomal-Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia

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Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

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The contribution of changes in the prevalence of prone sleeping position to the decline in sudden infant death syndrome in Tasmania

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Epidemiology of the sudden infant death syndrome: maternal, neonatal, and postneonatal risk factors

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Identifiers

DOI

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PubMed publication ID

22307399

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