(Q28292102)

2

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A Früh

3

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O-G Anfinsen

4

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K Gjesdal

5

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G Siem

6

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N Oyen

7

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G Greve

8

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A Carlsson

9

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T O Rognum

10

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M Hallerud

11

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E Kongsgård

12

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J P Amlie

13

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T P Leren

Scandinavian Journal of Clinical and Laboratory Investigation

14

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language of work or name

English

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publication date

2008

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published in

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volume

68

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issue

5

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page(s)

362-8

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cites work

The long QT syndrome. Prospective longitudinal study of 328 families

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

21 January 2018

1 reference

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Diagnostic criteria for the long QT syndrome. An update

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

Catecholamine-induced T-wave lability in congenital long QT syndrome: a novel phenomenon associated with syncope and cardiac arrest

21 January 2018

1 reference

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Risk stratification in the long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

The long QT syndrome: ion channel diseases of the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death

21 January 2018

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Task Force on Sudden Cardiac Death of the European Society of Cardiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

The congenital long QT syndromes from genotype to phenotype: clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

Human non-synonymous SNPs: server and survey

21 January 2018

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

21 January 2018

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

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365510701765643

Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

21 January 2018

1 reference

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Family and population strategies for screening and counselling of inherited cardiac arrhythmias

21 January 2018

1 reference

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Female predominance and transmission distortion in the long-QT syndrome.

21 January 2018

1 reference

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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

21 January 2018

1 reference

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Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases

21 January 2018

1 reference

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10.1080/00365510701765643

21 January 2018

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

18752142

1 reference

Consolidated OpenCitations Corpus – April 2017