Concealed long QT syndrome and intractable partial epilepsy: a case report (Q33161883)

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scientific article published on 8 October 2012

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Language	Label	Description	Also known as
English	Concealed long QT syndrome and intractable partial epilepsy: a case report	scientific article published on 8 October 2012

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scholarly article

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Europe PubMed Central

PubMed publication ID

23058853

retrieved

23 July 2017

case report

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title

Concealed long QT syndrome and intractable partial epilepsy: a case report (English)

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Europe PubMed Central

PubMed publication ID

23058853

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23 July 2017

main subject

long QT syndrome

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based on heuristic

inferred from title

author

Jason H. Anderson

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Jason H Anderson

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1

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Michael J Ackerman

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5

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Michael J Ackerman

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Europe PubMed Central

PubMed publication ID

23058853

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23 July 2017

author name string

Johan Martijn Bos

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2

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Europe PubMed Central

PubMed publication ID

23058853

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23 July 2017

Fredric B Meyer

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3

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Europe PubMed Central

PubMed publication ID

23058853

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23 July 2017

Gregory D Cascino

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4

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Europe PubMed Central

PubMed publication ID

23058853

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23 July 2017

language of work or name

English

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publication date

8 October 2012

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Europe PubMed Central

PubMed publication ID

23058853

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23 July 2017

published in

Mayo Clin Proc

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Europe PubMed Central

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23058853

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23 July 2017

volume

87

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Europe PubMed Central

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23058853

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23 July 2017

issue

11

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Europe PubMed Central

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23058853

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23 July 2017

page(s)

1128-1131

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Europe PubMed Central

PubMed publication ID

23058853

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23 July 2017

cites work

Sudden cardiac arrest without overt heart disease

1 reference

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PubMed Central

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

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PubMed Central

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21 June 2018

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532686

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21 June 2018

Seizures and arrhythmias: Differing phenotypes of a common channelopathy?

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PubMed Central

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21 June 2018

Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy

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PubMed Central

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ACC/AHA/HRS 2008 guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: executive summary

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21 June 2018

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

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21 June 2018

Implantable cardioverter defibrillator in high-risk long QT syndrome patients

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PubMed Central

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Impaired K(+) homeostasis and altered electrophysiological properties of post-traumatic hippocampal glia

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21 June 2018

The inherited long QT syndrome: from ion channel to bedside

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21 June 2018

The long QT syndrome: ion channel diseases of the heart

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21 June 2018

Reduction of K+ uptake in glia prevents long-term depression maintenance and causes epileptiform activity.

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21 June 2018

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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21 June 2018

A family of potassium channel genes related to eag in Drosophila and mammals

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21 June 2018

Magnetic resonance imaging-based volume studies in temporal lobe epilepsy: pathological correlations

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21 June 2018

Syncope--brain or heart? A case report

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532686

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21 June 2018

Identifiers

DOI

10.1016/J.MAYOCP.2012.07.019

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23058853

retrieved

23 July 2017

PMC publication ID

3532686

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23058853

retrieved

23 July 2017

PubMed publication ID

23058853

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23058853

retrieved

23 July 2017

ResearchGate publication ID

232235227

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