(Q36702826)

15 August 2017

1 reference

title

Long and short QT syndrome (English)

1 reference

15 August 2017

Borchert B

1

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15 August 2017

Lawrenz T

series ordinal

2

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15 August 2017

Stellbrink C

series ordinal

3

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15 August 2017

publication date

1 December 2006

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Herzschrittmachertherapie & Elektrophysiologie

15 August 2017

published in

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15 August 2017

volume

17

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15 August 2017

issue

4

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15 August 2017

page(s)

205-210

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

15 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00399-006-0534-9

Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00399-006-0534-9

Long-term follow-up of patients with long-QT syndrome treated with beta-blockers and continuous pacing

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00399-006-0534-9

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

21 January 2018

1 reference

12 December 2020

Short QT syndrome: successful prevention of sudden cardiac death in an adolescent by implantable cardioverter-defibrillator treatment for primary prophylaxis.

1 reference

12 December 2020

Pharmacological rescue of human K(+) channel long-QT2 mutations: human ether-a-go-go-related gene rescue without block

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Low penetrance in the long-QT syndrome: clinical impact

1 reference

12 December 2020

Clinical implications for affected parents and siblings of probands with long-QT syndrome.

1 reference

12 December 2020

Cost-effectiveness analysis of genetic testing for familial long QT syndrome in symptomatic index cases

1 reference

12 December 2020

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

1 reference

12 December 2020

ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death--executive summary: A report of the American College of Cardiology/American Heart Association Task Force and the European S

1 reference

12 December 2020

Susceptibility genes and modifiers for cardiac arrhythmias

1 reference

12 December 2020

Risk assessment in long QT syndrome: the Achilles heel of appropriate treatment.

1 reference

12 December 2020

A cardiac arrhythmia syndrome caused by loss of ankyrin-B function

1 reference

12 December 2020

25th anniversary of the International Long-QT Syndrome Registry: an ongoing quest to uncover the secrets of long-QT syndrome

1 reference

12 December 2020

Idiopathic short QT interval: a new clinical syndrome?

1 reference

12 December 2020

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

1 reference

12 December 2020

Short QT Syndrome: a familial cause of sudden death

1 reference

12 December 2020

Somatic gene and cell therapy strategies for the treatment of cardiac arrhythmias

1 reference

12 December 2020

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

1 reference

12 December 2020

The short QT syndrome as a paradigm to understand the role of potassium channels in ventricular fibrillation

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

1 reference

12 December 2020

Inherited arrhythmia syndromes: applying the molecular biology and genetic to the clinical management.

1 reference

12 December 2020

Risk stratification in the long-QT syndrome.

1 reference

12 December 2020

Implantable cardioverter-defibrillator therapy in patients with congenital long-QT syndrome: a long-term follow-up

1 reference

12 December 2020

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

1 reference

12 December 2020

Novel mutation in the Per-Arnt-Sim domain of KCNH2 causes a malignant form of long-QT syndrome.

1 reference

12 December 2020

1 reference

12 December 2020

Short QT syndrome or Andersen syndrome: Yin and Yang of Kir2.1 channel dysfunction

1 reference

12 December 2020

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

1 reference

12 December 2020

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

1 reference

12 December 2020

Short QT syndrome: pharmacological treatment

1 reference

12 December 2020

Long QT syndrome: from channels to cardiac arrhythmias

1 reference

12 December 2020

10.1007/S00399-006-0534-9

Identifiers

DOI

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15 August 2017

1 reference