Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Novel risk predictor of arrhythmias for patients with potassium channel related congenital Long-QT Syndrome.

Autor: Juarez CK; Department of Experimental Cardiology, Heart Centre, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, the Netherlands., Proost VM; Department of Experimental Cardiology, Heart Centre, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, the Netherlands., Tanck MW; Department of Epidemiology and Data Science, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, the Netherlands., Dittmann S; Institute for Genetics of Heart Diseases, University Hospital Münster, Münster, Germany., Bos JM; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology & Experimental Therapeutics, Division of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, USA., Crotti L; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy; Department of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy., Barc J; Nantes Université, CNRS, INSERM, l'institut du thorax, F-44000 Nantes, France; Member of the European Reference Network for rare, low prevalence and complex diseases of the heart: ERN GUARD-Heart., van den Berg MP; Department of Cardiology, University Medical Centre Groningen, University of Groningen, The Netherlands., Mujkanovic J; The Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Denmark; Department of Forensic Medicine, Faculty of Health and Medical Sciences, Copenhagen, Denmark., Rickert C; Institute for Genetics of Heart Diseases, University Hospital Münster, Münster, Germany., Lopes Neves RA; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology & Experimental Therapeutics, Division of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, USA., Musu G; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy., Dagradi F; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy., Giovenzana FLF; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy., Clédel A; Nantes Université, CNRS, INSERM, l'institut du thorax, F-44000 Nantes, France., Thollet A; Nantes Université, CNRS, INSERM, l'institut du thorax, F-44000 Nantes, France., Giudicessi JR; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology & Experimental Therapeutics, Division of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, USA., Tfelt-Hansen J; The Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Denmark; Member of the European Reference Network for rare, low prevalence and complex diseases of the heart: ERN GUARD-Heart., Probst V; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, F-44000 Nantes, France; Member of the European Reference Network for rare, low prevalence and complex diseases of the heart: ERN GUARD-Heart., Schwartz PJ; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy., Ackerman MJ; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology & Experimental Therapeutics, Division of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, USA., Schulze-Bahr E; Institute for Genetics of Heart Diseases, University Hospital Münster, Münster, Germany; Member of the European Reference Network for rare, low prevalence and complex diseases of the heart: ERN GUARD-Heart., Bezzina CR; Department of Experimental Cardiology, Heart Centre, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, the Netherlands; Member of the European Reference Network for rare, low prevalence and complex diseases of the heart: ERN GUARD-Heart., Wilde AAM; Department of Experimental Cardiology, Heart Centre, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, the Netherlands; Member of the European Reference Network for rare, low prevalence and complex diseases of the heart: ERN GUARD-Heart. Electronic address: a.a.wilde@amsterdamumc.nl.

Publikováno v: Heart rhythm [Heart Rhythm] 2024 Dec 13. Date of Electronic Publication: 2024 Dec 13.