Cardiac channelopathies and sudden infant death syndrome (Q37903593)

25 August 2017

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title

Cardiac channelopathies and sudden infant death syndrome (English)

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25 August 2017

1

Jacob Tfelt-Hansen

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Bo Gregers Winkel

series ordinal

2

object named as

Bo Gregers Winkel

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25 August 2017

Thomas Jespersen

4

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author name string

Morten Grunnet

series ordinal

3

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25 August 2017

language of work or name

English

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publication date

16 July 2011

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25 August 2017

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25 August 2017

volume

119

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25 August 2017

issue

1

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25 August 2017

page(s)

21-33

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Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

25 August 2017

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Sudden infant death syndrome: do ion channels play a role?

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A molecular link between the sudden infant death syndrome and the long-QT syndrome

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Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

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Sudden death associated with short-QT syndrome linked to mutations in HERG.

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Cardiac sodium channel dysfunction in sudden infant death syndrome.

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A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors

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Inherited cardiac diseases caused by mutations in the Nav1.5 sodium channel

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Cardiac potassium channel dysfunction in sudden infant death syndrome

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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current

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Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome

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Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3

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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

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De novo mutation in the SCN5A gene associated with early onset of sudden infant death

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Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A.

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Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

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A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

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Cardiac ion channel gene mutations in sudden infant death syndrome

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Clinical aspects and prognosis of Brugada syndrome in children

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Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation

21 January 2018

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GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A

21 January 2018

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Restricting excessive cardiac action potential and QT prolongation: a vital role for IKs in human ventricular muscle.

21 January 2018

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Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels

21 January 2018

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Short QT Syndrome: a familial cause of sudden death

21 January 2018

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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

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A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.

21 January 2018

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Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis

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Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

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Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

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Basolateral localisation of KCNQ1 potassium channels in MDCK cells: molecular identification of an N-terminal targeting motif

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Low incidence of sudden cardiac death in a Swedish Y111C type 1 long-QT syndrome population

21 January 2018

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Sudden infant death syndrome: how significant are the cardiac channelopathies?

21 January 2018

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Contribution of long-QT syndrome genetic variants in sudden infant death syndrome

21 January 2018

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Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome

21 January 2018

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A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine

21 January 2018

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Molecular diagnosis in a child with sudden infant death syndrome

21 January 2018

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Guidelines for the interpretation of the neonatal electrocardiogram

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000329047

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25 August 2017

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