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Andersen-Tawil syndrome
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Andersen-Tawil syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
author name string
Andrew H Smith
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Frank A Fish
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Prince J Kannankeril
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
language of work or name
English
0 references
publication date
1 January 2006
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
published in
Indian Pacing and Electrophysiology Journal
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
volume
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
page(s)
32-43
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
cites work
Genetics of acquired long QT syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Recent advances in understanding sex differences in cardiac repolarization.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
The inward rectifier current (IK1) controls cardiac excitability and is involved in arrhythmogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Polymorphic ventricular tachycardia and KCNJ2 mutations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Mapping and ablation of ventricular fibrillation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Mapping and ablation of ventricular fibrillation associated with long-QT and Brugada syndromes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Functional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Q28207558
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Molecular biology and the prolonged QT syndromes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Andersen syndrome autosomal dominant in three generations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
A comparison of antiarrhythmic-drug therapy with implantable defibrillators in patients resuscitated from near-fatal ventricular arrhythmias
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Structure and function of cardiac sodium and potassium channels
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Molecular cloning and expression of a human heart inward rectifier potassium channel
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Primary structure and functional expression of a mouse inward rectifier potassium channel
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Identification of a mutation in the gene causing hyperkalemic periodic paralysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
7 July 2018
Suppression of bidirectional ventricular tachycardia and unmasking of prolonged QT interval with verapamil in Andersen's syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
26 October 2018
Andersen mutations of KCNJ2 suppress the native inward rectifier current IK1 in a dominant-negative fashion.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
26 October 2018
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
26 October 2018
Amiodarone and acetazolamide for the treatment of genetically confirmed severe Andersen syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
26 October 2018
Determination of the subunit stoichiometry of an inwardly rectifying potassium channel
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1501096
retrieved
26 October 2018
J Periodic paralysis with cardiac arrhythmia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16943893
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hypokalemic periodic paralysis with arrhythmia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16943893
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
KCNJ2 mutation in intractable ventricular arrhythmia with Andersen's syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16943893
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cases from the Osler Medical Service at Johns Hopkins University. Digitalis toxicity with bidirectional ventricular tachycardia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16943893
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1501096
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
PubMed publication ID
16943893
1 reference
stated in
Europe PubMed Central
PMC publication ID
1501096
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16943893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
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