Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia (Q28661099)

21 June 2017

title

Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia (English)

1 reference

21 June 2017

0 references

1 reference

1 reference

Arthur A M Wilde

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21 June 2017

Zahurul A Bhuiyan

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21 June 2017

Safar Al-Shahrani

series ordinal

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21 June 2017

Jumana Al-Aama

series ordinal

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21 June 2017

Tarek S Momenah

series ordinal

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21 June 2017

language of work or name

English

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publication date

20 November 2013

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21 June 2017

published in

Frontiers in pediatrics

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21 June 2017

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21 June 2017

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Identification of a Kir3.4 mutation in congenital long QT syndrome

21 June 2017

cites work

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A common polymorphism associated with antibiotic-induced cardiac arrhythmia

17 March 2017

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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

17 March 2017

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A single Na(+) channel mutation causing both long-QT and Brugada syndromes

17 March 2017

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

17 March 2017

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Mutation of the Gene for I sK Associated With Both Jervell and Lange-Nielsen and Romano-Ward Forms of Long-QT Syndrome

17 March 2017

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Mutations in the hminK gene cause long QT syndrome and suppress lKs function

17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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Molecular cloning and expression of a human heart inward rectifier potassium channel

17 March 2017

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Primary structure and functional expression of a mouse inward rectifier potassium channel

17 March 2017

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Mapping of a gene for long QT syndrome to chromosome 4q25-27

17 March 2017

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A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome

17 March 2017

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Maternal mosaicism confounds the neonatal diagnosis of type 1 Timothy syndrome

3 June 2018

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Risk of life-threatening cardiac events among patients with long QT syndrome and multiple mutations

3 June 2018

1 reference

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Not all beta-blockers are equal in the management of long QT syndrome types 1 and 2: higher recurrence of events under metoprolol

3 June 2018

1 reference

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Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications

3 June 2018

1 reference

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Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to β-blocker therapy in type 1 long-QT syndrome

3 June 2018

1 reference

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Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3864249

A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes

3 June 2018

1 reference

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Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndrome

3 June 2018

1 reference

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

3 June 2018

1 reference

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Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.

3 June 2018

1 reference

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Prevalence of the congenital long-QT syndrome.

3 June 2018

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Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?

3 June 2018

1 reference

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An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome

3 June 2018

1 reference

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The cardiac sodium channel mutation delQKP 1507-1509 is associated with the expanding phenotypic spectrum of LQT3, conduction disorder, dilated cardiomyopathy, and high incidence of youth sudden death

3 June 2018

1 reference

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The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

3 June 2018

1 reference

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Long-QT syndrome after age 40.

3 June 2018

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Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

3 June 2018

1 reference

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Clinical practice. Long-QT syndrome

3 June 2018

1 reference

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A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance

3 June 2018

1 reference

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

3 June 2018

1 reference

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Long QT syndrome and pregnancy

3 June 2018

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Drug-induced long QT and torsade de pointes: recent advances

3 June 2018

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The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome

3 June 2018

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

3 June 2018

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Genetics of cardiac arrhythmias

3 June 2018

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KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome

3 June 2018

1 reference

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Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndrome

3 June 2018

1 reference

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Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome

3 June 2018

1 reference

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Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations

3 June 2018

1 reference

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A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3864249

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

3 June 2018

1 reference

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Risk stratification in the long-QT syndrome.

3 June 2018

1 reference

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

3 June 2018

1 reference

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Localization of sodium channels in intercalated disks modulates cardiac conduction

3 June 2018

1 reference

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Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

3 June 2018

1 reference

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Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel

3 June 2018

1 reference

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Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family

3 June 2018

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

3 June 2018

1 reference

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Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block

3 June 2018

1 reference

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

3 June 2018

1 reference

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

3 June 2018

1 reference

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Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome

3 June 2018

1 reference

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Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).

3 June 2018

1 reference

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

3 June 2018

1 reference

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Mechanisms and management of proarrhythmia

3 June 2018

1 reference

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3 June 2018

1 reference

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Diagnostic criteria for the long QT syndrome. An update

3 June 2018

1 reference

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Idiopathic long QT syndrome: asking the right question

3 June 2018

1 reference

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Consanguinity among the Saudi Arabian population

3 June 2018

1 reference

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Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes

3 June 2018

1 reference

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IKs in heart and hearing, the ear can do with less than the heart

27 November 2018

1 reference

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Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: expanding the spectrum of Timothy syndrome

27 November 2018

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D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome

27 November 2018

1 reference

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Consanguinity and major genetic disorders in Saudi children: a community-based cross-sectional study.

27 November 2018

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Contribution of inherited heart disease to sudden cardiac death in childhood.

27 November 2018

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Postmortem long QT syndrome genetic testing for sudden unexplained death in the young

27 November 2018

1 reference

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Cardiac sodium channel dysfunction in sudden infant death syndrome.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3864249

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3864249

Mutations in the HERG K+-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3864249

Compound mutations: a common cause of severe long-QT syndrome

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3864249

Homozygous premature truncation of the HERG protein : the human HERG knockout

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3864249

The long QT syndrome with impaired atrioventricular conduction: a malignant variant in infants.

27 November 2018

1 reference

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Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3864249

Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes

27 November 2018

1 reference

12 December 2020

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

1 reference

12 December 2020

Anti-KCNH2 antibody-induced long QT syndrome: novel acquired form of long QT syndrome

1 reference

12 December 2020

Genotype-specific onset of arrhythmias in congenital long-QT syndrome: possible therapy implications

1 reference

12 December 2020

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

1 reference

12 December 2020

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

1 reference

12 December 2020

Molecular crosstalk between mechanical and electrical junctions at the intercalated disc

1 reference

12 December 2020

Slow delayed rectifier potassium current blockade contributes importantly to drug-induced long QT syndrome

1 reference

12 December 2020

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

1 reference

12 December 2020

A newborn with a complex congenital heart disease, atrioventricular block, and torsade de pointes ventricular tachycardia

1 reference

12 December 2020

Molecular diagnosis in a child with sudden infant death syndrome

1 reference

12 December 2020

[Task Force on Sudden Cardiac Death, European Society of Cardiology. Summary of recommendations]

1 reference

12 December 2020

De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome

1 reference

12 December 2020

Identifiers

DOI

10.3389/FPED.2013.00039

1 reference

release_2knyrdzpqff7djbr2wlrbnocvy

21 June 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2knyrdzpqff7djbr2wlrbnocvy

24 November 2022

mapped directly with Wikidata item

PMC publication ID

3864249

0 references

1 reference