Search details
1.
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation
; 142(4): 324-338, 2020 07 28.
Article
in English
| MEDLINE | ID: mdl-32429735
2.
POPDC2 a novel susceptibility gene for conduction disorders.
J Mol Cell Cardiol
; 145: 74-83, 2020 08.
Article
in English
| MEDLINE | ID: mdl-32535041
3.
A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction.
Circ Res
; 120(10): e33-e44, 2017 May 12.
Article
in English
| MEDLINE | ID: mdl-28219978
4.
Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking.
Eur Heart J
; 37(7): 640-50, 2016 Feb 14.
Article
in English
| MEDLINE | ID: mdl-26271031
5.
Corneal Densitometry as a Novel Technique for Monitoring Amiodarone Therapy.
Ophthalmology
; 123(11): 2294-2299, 2016 11.
Article
in English
| MEDLINE | ID: mdl-27591052
6.
Tpeak-Tend interval and Tpeak-Tend/QT ratio in patients with Brugada syndrome.
Europace
; 18(12): 1866-1872, 2016 Dec.
Article
in English
| MEDLINE | ID: mdl-26941339
7.
Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia.
Europace
; 18(10): 1587-1592, 2016 Oct.
Article
in English
| MEDLINE | ID: mdl-26705564
8.
Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome.
J Mol Cell Cardiol
; 80: 186-95, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25633834
9.
Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype.
Basic Res Cardiol
; 108(3): 353, 2013 May.
Article
in English
| MEDLINE | ID: mdl-23644778
10.
Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbances.
Hum Mutat
; 33(1): 109-17, 2012 Jan.
Article
in English
| MEDLINE | ID: mdl-21887725
11.
Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channel.
Cell Physiol Biochem
; 29(5-6): 809-18, 2012.
Article
in English
| MEDLINE | ID: mdl-22613981
12.
(Tpeak - Tend)/QRS and (Tpeak - Tend)/(QT × QRS) as risk markers in Brugada syndrome: authors' reply.
Europace
; 19(4): 696-697, 2017 04 01.
Article
in English
| MEDLINE | ID: mdl-28398527
13.
Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: a long-term follow-up.
Europace
; 14(3): 396-401, 2012 Mar.
Article
in English
| MEDLINE | ID: mdl-21979994
14.
Totally subcutaneous implantable cardioverter defibrillator with an alternative, right parasternal, electrode placement.
Pacing Clin Electrophysiol
; 35(9): e254-7, 2012 Sep.
Article
in English
| MEDLINE | ID: mdl-21401656
15.
Genes causing inherited forms of cardiomyopathies. A current compendium.
Herz
; 34(2): 98-109, 2009 Mar.
Article
in English
| MEDLINE | ID: mdl-19370325
16.
Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K+ Channel) Channel Function.
Circ Genom Precis Med
; 12(1): e002238, 2019 01.
Article
in English
| MEDLINE | ID: mdl-30645171
17.
Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography.
Heart
; 104(4): 332-339, 2018 02.
Article
in English
| MEDLINE | ID: mdl-28864717
18.
Sodium permeable and "hypersensitive" TREK-1 channels cause ventricular tachycardia.
EMBO Mol Med
; 9(4): 403-414, 2017 04.
Article
in English
| MEDLINE | ID: mdl-28242754
19.
Long-term follow-up of subcutaneous ICD systems in patients with hypertrophic cardiomyopathy: a single-center experience.
Clin Res Cardiol
; 105(1): 89-93, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-26233714
20.
Intraoperative Defibrillation Testing of Subcutaneous Implantable Cardioverter-Defibrillator Systems-A Simple Issue?
J Am Heart Assoc
; 5(3): e003181, 2016 Mar 15.
Article
in English
| MEDLINE | ID: mdl-27068637