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Eric Schulze-Bahr

Research Profile

Disorders

Physiology

Chemicals & Drugs

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DNA Mutational Analysis

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Defibrillators, Implantable

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TOP 3
Matthias Paul; Horst Robenek; Eric Schulze-Bahr; Volker Arps; Günter Breithardt; Joachim Gerss; Thomas Wichter; Gabriele Weissen-Plenz
Connexin expression patterns in arrhythmogenic right ventricular cardiomyopathy.
Maren M Limberg; Michael F Netter; Susanne Rinné; Jane Rogers; Doris Böckelmann; Alison J Coffey; Niels Decher; Andrew Grace; Birgit Stallmeyer; Sven Zumhagen; Eric Schulze-Bahr
Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype.
Alexander Samol; Eric Schulze-Bahr; Christian Vahlhaus; Thomas Wichter; Christian G Wollmann; Günter Breithardt; Hans-Jürgen Bruns; Joachim Gerss; Matthias Paul
T-wave integral: an electrocardiographic marker discriminating patients with arrhythmogenic right ventricular cardiomyopathy from patients with right ventricular outflow tract tachycardia.

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2013: Matthias Paul; Horst Robenek; Eric Schulze-Bahr; Volker Arps; Günter Breithardt; Joachim Gerss; Thomas Wichter; Gabriele Weissen-Plenz
Connexin expression patterns in arrhythmogenic right ventricular cardiomyopathy.
The American journal of cardiology 2013;111(10):1488-95.
2013: Maren M Limberg; Michael F Netter; Susanne Rinné; Jane Rogers; Doris Böckelmann; Alison J Coffey; Niels Decher; Andrew Grace; Birgit Stallmeyer; Sven Zumhagen; Eric Schulze-Bahr
Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype.
Basic research in cardiology 2013;108(3):353.
2013: Alexander Samol; Eric Schulze-Bahr; Christian Vahlhaus; Thomas Wichter; Christian G Wollmann; Günter Breithardt; Hans-Jürgen Bruns; Joachim Gerss; Matthias Paul
T-wave integral: an electrocardiographic marker discriminating patients with arrhythmogenic right ventricular cardiomyopathy from patients with right ventricular outflow tract tachycardia.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2013;15(4):582-9.
2012: Matthias Paul; Eric Schulze-Bahr; J Waltenberger; Thomas Wichter; Larissa Fabritz; Paulus Kirchhof
Arrhythmogenic right ventricular cardiomyopathy: an update on pathophysiology, genetics, diagnosis, and risk stratification.
Herzschrittmachertherapie & Elektrophysiologie 2012;23(3):186-95.
2012: Sven Zumhagen; Lars Eckardt; Corinna Friedrich; Guiscard Seebohm; Birgit Stallmeyer; Eric Schulze-Bahr
Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy.
Herzschrittmachertherapie & Elektrophysiologie 2012;23(3):211-9.
2012: G Frommeyer; C Pott; Eric Schulze-Bahr; Lars Eckardt
[Catecholaminergic polymorphic ventricular tachycardia].
Herzschrittmachertherapie & Elektrophysiologie 2012;23(3):231-6.
2012: Sven Zumhagen; Lars Eckardt; Andrew A Grace; Julia Köbe; Andreas Löher; Stephen O'Connor; Eric Schulze-Bahr
Totally subcutaneous implantable cardioverter defibrillator with an alternative, right parasternal, electrode placement.
Pacing and clinical electrophysiology : PACE 2012;35(9):e254-7.
2012: Simon Kochhäuser; Eric Schulze-Bahr; Uwe Kirchhefer
Arrhythmia-associated cardiac Ca²(+) cycling proteins and gene mutations.
Wiener medizinische Wochenschrift (1946) 2012;162(13-14):292-6.
2012: Birgit Stallmeyer; Matthias Koopmann; Eric Schulze-Bahr
Identification of novel mutations in LMNA associated with familial forms of dilated cardiomyopathy.
Genetic testing and molecular biomarkers 2012;16(6):543-9.
2012: Christian Geier; Eric Schulze-Bahr; Gisèle Bonne
Guiding the molecular diagnosis of hypertrophic cardiomyopathy.
The Journal of thoracic and cardiovascular surgery 2012;143(5):1234.
2012: Matthias Paul; Kambiz Rahbar; Klaus P Schäfers; Günter Breithardt; Joachim Gerss; Peter Kies; Otmar Schober; Eric Schulze-Bahr; Thomas Wichter; Michael Schäfers
Microvascular dysfunction in nonfailing arrhythmogenic right ventricular cardiomyopathy.
European journal of nuclear medicine and molecular imaging 2012;39(3):416-20.
2012: Gerold Mönnig; Christian Pott; Razvan Radu; Hans H Scheld; Eric Schulze-Bahr; Kristina Wasmer; Stephan Zellerhoff; Sven Zumhagen; Wilhelm Haverkamp; Julia Köbe; Andreas Löher; Peter Milberg; Lars Eckardt
Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: a long-term follow-up.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2012;14(3):396-401.
2012: Ulrike Henrion; Florian Lang; Eric Schulze-Bahr; Birgit Stallmeyer; Katja Steinke; Nathalie Strutz-Seebohm; Sven Zumhagen; Guiscard Seebohm
Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channel.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2012;29(5-6):809-18.
2011: Matthias Paul; Eric Schulze-Bahr; Jörg Stypmann; Günter Breithardt; Joachim Gerss; Sophia Wirdeier; Sven Zumhagen; Thomas Wichter
Safety of endomyocardial biopsy in patients with arrhythmogenic right ventricular cardiomyopathy: a study analyzing 161 diagnostic procedures.
JACC. Cardiovascular interventions 2011;4(10):1142-8.
2011: Julia Köbe; F Reinke; Eric Schulze-Bahr; S Zumhagen; Lars Eckardt
[Totally subcutaneous cardioverter-defibrillator (S-ICD®) : recent experience and future perspectives].
Herz 2011;36(7):586-91.
2011: Matthias Paul; Kambiz Rahbar; Günter Breithardt; Lars Eckardt; Joachim Gerss; Peter Kies; Otmar Schober; Eric Schulze-Bahr; Thomas Wichter; Christian G Wollmann; Michael Schäfers
Cardiac sympathetic dysfunction in genotyped patients with arrhythmogenic right ventricular cardiomyopathy and risk of recurrent ventricular tachyarrhythmias.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2011;52(10):1559-65.
2011: Peter Kies; Gerold Mönnig; Matthias Paul; Michael Schäfers; Otmar Schober; Lars Stegger; Thomas Wichter; Joachim Gerss; Eric Schulze-Bahr
Impaired cardiac sympathetic innervation in symptomatic patients with long QT syndrome.
European journal of nuclear medicine and molecular imaging 2011;38(10):1899-907.
2011: Michael J Ackerman; Charles Berul; Ramon Brugada; Hugh Calkins; A John Camm; Patrick T Ellinor; Michael Gollob; Robert Hamilton; Ray E Hershberger; Daniel P Judge; Hervè Le Marec; William J McKenna; Silvia G Priori; Eric Schulze-Bahr; Chris Semsarian; Jeffrey A Towbin; Hugh Watkins; Arthur Wilde; Stephan Willems; Christian Wolpert; Douglas P Zipes
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2011;13(8):1077-109.
2011: Michael J Ackerman; Charles Berul; Ramon Brugada; Hugh Calkins; A John Camm; Patrick T Ellinor; Michael Gollob; Robert Hamilton; Ray E Hershberger; Daniel P Judge; Hervè Le Marec; William J McKenna; Silvia G Priori; Eric Schulze-Bahr; Chris Semsarian; Jeffrey A Towbin; Hugh Watkins; Arthur Wilde; Stephan Willems; Christian Wolpert; Douglas P Zipes
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).
Heart rhythm : the official journal of the Heart Rhythm Society 2011;8(8):1308-39.
2011: Christian Pott; Dirk G Dechering; Florian Reinke; Adam Muszynski; Stephan Zellerhoff; Alex Bittner; Julia Köbe; Kristina Wasmer; Eric Schulze-Bahr; Gerold Mönnig; Stefan Kotthoff; Lars Eckardt
Successful treatment of catecholaminergic polymorphic ventricular tachycardia with flecainide: a case report and review of the current literature.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2011;13(6):897-901.
2010: Stephan Zellerhoff; Martin Hinterseer; Bastian Felix Krull; Eric Schulze-Bahr; Larissa Fabritz; Günter Breithardt; Paulus Kirchhof; Stefan Kääb
Ivabradine in patients with inappropriate sinus tachycardia.
Naunyn-Schmiedeberg's archives of pharmacology 2010;382(5-6):483-6.
2010: Axel Neu; Michele Eiselt; Matthias Paul; Kathrin Sauter; Birgit Stallmeyer; Dirk Isbrandt; Eric Schulze-Bahr
A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.
Human mutation 2010;31(8):E1609-21.
2010: Uwe Kirchhefer; Diana Wehrmeister; Alex V Postma; Gottfried Pohlentz; Michael Mormann; Dana Kucerova; Frank U Müller; Wilhelm Schmitz; Eric Schulze-Bahr; Arthur A Wilde; Joachim Neumann
The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handling.
Journal of molecular and cellular cardiology 2010;49(1):95-105.
2010: Jamie D Kapplinger; David J Tester; Marielle Alders; Begoña Benito; Myriam Berthet; Josep Brugada; Pedro Brugada; Véronique Fressart; Alejandra Guerchicoff; Carole Harris-Kerr; Shiro Kamakura; Florence Kyndt; Tamara T Koopmann; Yoshihiro Miyamoto; Ryan Pfeiffer; Guido D Pollevick; Vincent Probst; Sven Zumhagen; Matteo Vatta; Jeffrey A Towbin; Wataru Shimizu; Eric Schulze-Bahr; Charles Antzelevitch; Salisbury Benjamin; Pascale Guicheney; Arthur A M Wilde; Ramon Brugada; Jean-Jacques Schott; Michael J Ackerman
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.
Heart rhythm : the official journal of the Heart Rhythm Society 2010;7(1):33-46.
2009: Moritz F Sinner; Arne Pfeufer; Siegfried Perz; Eric Schulze-Bahr; Gerold Mönnig; Lars Eckardt; britt beckmann; H-Erich Wichmann; Günter Breithardt; Gerhard Steinbeck; Larissa Fabritz; Stefan Kääb; Paulus Kirchhof
Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2009;11(10):1338-44.
2009: Martin Kruse; Eric Schulze-Bahr; Valerie Corfield; Alf Beckmann; Birgit Stallmeyer; Andersen Jerome; Iris Ohmert; Eric Schulze-Bahr; Paul Brink; Olaf Pongs
Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I.
The Journal of clinical investigation 2009;119(9):2737-44.
2009: Horst Wedekind; D Burde; S Zumhagen; Volker Debus; G Burkhardtsmaier; Gerold Mönnig; Günter Breithardt; Eric Schulze-Bahr
QT interval prolongation and risk for cardiac events in genotyped LQTS-index children.
European journal of pediatrics 2009;168(9):1107-15.
2009: Eric Schulze-Bahr
Making sense in a nonsense reading frame: suppression of cardiac sodium channel dysfunction.
Cardiovascular research 2009;83(3):423-4.
2009: Stephan Zellerhoff; Rudin Pistulli; Gerold Mönnig; Martin Hinterseer; britt beckmann; Julia Köbe; Gerhard Steinbeck; Stefan Kääb; Wilhelm Haverkamp; Larissa Fabritz; Rainer Gradaus; Günter Breithardt; Eric Schulze-Bahr; Dirk Böcker; Paulus Kirchhof
Atrial Arrhythmias in long-QT syndrome under daily life conditions: a nested case control study.
Journal of cardiovascular electrophysiology 2009;20(4):401-7.
2009: Matthias Paul; Sven Zumhagen; Birgit Stallmeyer; Matthias Koopmann; Tilmann Spieker; Eric Schulze-Bahr
Genes causing inherited forms of cardiomyopathies. A current compendium.
Herz 2009;34(2):98-109.
2009: Sven Zumhagen; Tilmann Spieker; Julia Rolinck; Hideo A Baba; Günter Breithardt; Werner Böcker; Lars Eckardt; Matthias Paul; Thomas Wichter; Eric Schulze-Bahr
Absence of pathognomonic or inflammatory patterns in cardiac biopsies from patients with Brugada syndrome.
Circulation. Arrhythmia and electrophysiology 2009;2(1):16-23.
2009: Nathalie Gaborit; Thomas Wichter; Andras Varro; Viktoria Szuts; guillaume lamirault; Lars Eckardt; Matthias Paul; Günter Breithardt; Eric Schulze-Bahr; Denis Escande; Stanley Nattel; Sophie Demolombe
Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseases.
European heart journal 2009;30(4):487-96.
2009: Michel Haïssaguerre; Stephanie Chatel; Frederic Sacher; Rukshen Weerasooriya; Vincent Probst; Gildas Loussouarn; Marc Horlitz; Ruedige Liersch; Eric Schulze-Bahr; Arthur Wilde; Stefan Kääb; Joseph Koster; Yoram Rudy; Hervé Le Marec; Jean Jacques Schott
Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel.
Journal of cardiovascular electrophysiology 2009;20(1):93-8.
2008: Eric Schulze-Bahr
Susceptibility genes & modifiers for cardiac arrhythmias.
Progress in biophysics and molecular biology 2008;98(2-3):289-300.
2008: Naomasa Makita; Elijah Behr; Wataru Shimizu; Minoru Horie; Akihiko Sunami; Lia Crotti; Eric Schulze-Bahr; Shigetomo Fukuhara; Naoki Mochizuki; Takeru Makiyama; Hideki Itoh; Michael Christiansen; Pascal McKeown; Koji Miyamoto; Shiro Kamakura; Hiroyuki Tsutsui; Peter J Schwartz; Alfred L George; Dan Mark Roden
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.
The Journal of clinical investigation 2008;118(6):2219-29.
2008: Matthias Paul; Eric Schulze-Bahr
Risk assessment in Brugada-syndrome: the way back to the surface ECG.
Journal of cardiovascular electrophysiology 2008;19(4):384-5.
2007: Lia Crotti; Carla Spazzolini; Peter J Schwartz; Wataru Shimizu; Isabelle Denjoy; Eric Schulze-Bahr; Elena V Zaklyazminskaya; Heikki Swan; Michael J Ackerman; Arthur J Moss; Arthur A M Wilde; Minoru Horie; Paul A Brink; Roberto Insolia; Gaetano M De Ferrari; Gabriele Crimi
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.
Circulation 2007;116(21):2366-75.
2007: Matthias Paul; Joachim Gerss; Eric Schulze-Bahr; Thomas Wichter; Christian Vahlhaus; Arthur A M Wilde; Günter Breithardt; Lars Eckardt
Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data.
European heart journal 2007;28(17):2126-33.
2007: Lisa Wingenfeld; Andreas Freislederer; Eric Schulze-Bahr; Matthias Paul; Thomas Bajanowski
Life-threatening hobbies in the youth? Two autoptic cases suggesting arrhythmogenic right ventricular cardiomyopathy.
Forensic science international 2007;171(1):e1-4.
2007: Eric Schulze-Bahr
Cardiac sodium channels: dysregulation meets myocardial failure.
Cardiovascular research 2007;75(3):455-6.
2007: Horst Wedekind; Eric Schulze-Bahr; Volker Debus; Günter Breithardt; Bernd Brinkmann; Thomas Bajanowski
Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigation.
International journal of legal medicine 2007;121(4):245-57.
2007: Nicole Schmitt; Kirstine Calloe; Nathalie Hélix Nielsen; Maria Buschmann; Erwin-Josef Speckmann; Eric Schulze-Bahr; Martin Schwarz
The novel C-terminal KCNQ1 mutation M520R alters protein trafficking.
Biochemical and biophysical research communications 2007;358(1):304-10.
2007: Stefan Peters; Eric Schulze-Bahr; Susan P Etheridge; Martin Tristani-Firouzi
Sudden cardiac death in Andersen-Tawil syndrome.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2007;9(3):162-6.
2006: Medea Imboden; Heikki Swan; Isabelle Denjoy; Irene van Langen; Päivi Johanna Latinen-Forsblom; Carlo Napolitano; Véronique Fressart; Guenter Breithardt; Myriam Berthet; Silvia Priori; Bernard Hainque; Arthur Arnold Maria Wilde; Eric Schulze-Bahr; JOSUE FEINGOLD; Pascale Guicheney
Female predominance and transmission distortion in the long-QT syndrome.
The New England journal of medicine 2006;355(26):2744-51.
2006: Hanno L Tan; Abdennasser Bardai; Wataru Shimizu; Arthur J Moss; Eric Schulze-Bahr; Takashi Noda; Arthur A M Wilde
Genotype-specific onset of arrhythmias in congenital long-QT syndrome: possible therapy implications.
Circulation 2006;114(20):2096-103.
2006: Chi-un Choe; Eric Schulze-Bahr; Axel Neu; Jun Xu; Zheng I Zhu; Kathrin Sauter; Robert Bähring; Silvia Priori; Pascale Guicheney; Gerold Mönnig; Carlo Neapolitano; Jan Heidemann; colleen clancy; Olaf Pongs; Dirk Isbrandt
C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon.
Human molecular genetics 2006;15(19):2888-902.
2006: Gerold Mönnig; Lars Eckardt; Horst Wedekind; Wilhelm Haverkamp; Joachim Gerss; Peter Milberg; Kristina Wasmer; Paulus Kirchhof; Gerd Assmann; Günter Breithardt; Eric Schulze-Bahr
Electrocardiographic risk stratification in families with congenital long QT syndrome.
European heart journal 2006;27(17):2074-80.
2006: Eric Schulze-Bahr
Mutation detection beyond: an example from congenital long QT syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2006;3(7):822-3.
2006: Horst Wedekind; Thomas Bajanowski; Patrick Friederich; Günter Breithardt; Thomas Wülfing; Cornelia C Siebrands; Birgit Engeland; Gerold Mönnig; Wilhelm Haverkamp; Bernd Brinkmann; Eric Schulze-Bahr
Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.
International journal of legal medicine 2006;120(3):129-37.
2006: Dörte Etzrodt; Eric Schulze-Bahr
Letter regarding article by Burke et al, "role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks".
Circulation 2006;113(15):e709; author reply e709.
2006: Eric Schulze-Bahr
[Short QT Syndromes].
Herz 2006;31(2):118-22; quiz 142-3.
2006: Peter J Schwartz; Carla Spazzolini; Lia Crotti; Jørn Bathen; Jan P Amlie; Katherine W Timothy; Maria Shkolnikova; Charles I Berul; Maria Bitner-Glindzicz; Lauri Toivonen; Minoru Horie; Eric Schulze-Bahr; Isabelle Denjoy
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome.
Circulation 2006;113(6):783-90.
2005: Hans Gerd Kehl; Volker Debus; D Stege; T D T Tjan; Johannes Vogt; Eric Schulze-Bahr
[Atrial flutter after orthotopic heart transplantation due to recipient-to-donor transatrial conduction].
Herzschrittmachertherapie & Elektrophysiologie 2005;16(4):270-3.
2005: Matthias Paul; Eric Schulze-Bahr; Lars Eckardt; Günter Breithardt; Thomas Wichter
[Right ventricular tachyarrhythmias--diagnostics and therapy].
Herzschrittmachertherapie & Elektrophysiologie 2005;16(4):260-9.
2005: Arie O Verkerk; Ronald Wilders; Eric Schulze-Bahr; Leander Beekman; Zahurul A Bhuiyan; Jessica Bertrand; Lars Eckardt; Dongxin Lin; Martin Borggrefe; Günter Breithardt; marcel mannens; Hanno L Tan; Arthur A M Wilde; Connie R Bezzina
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome.
Cardiovascular research 2005;68(3):441-53.
2005: Jeroen P P Smits; Marieke W Veldkamp; Connie R Bezzina; Zahurul A Bhuiyan; Horst Wedekind; Eric Schulze-Bahr; Arthur A M Wilde
Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome.
Cardiovascular research 2005;67(3):459-66.
2005: Stefan Kääb; Eric Schulze-Bahr
Susceptibility genes and modifiers for cardiac arrhythmias.
Cardiovascular research 2005;67(3):397-413.
2005: Eric Schulze-Bahr; Paulus Kirchhof; Lars Eckardt; Jessica Bertrand; Günter Breithardt
Gender differences in cardiac arrhythmias.
Herz 2005;30(5):390-400.
2005: Gerold Mönnig; Julia Köbe; Andreas Löher; Lars Eckardt; Horst Wedekind; Hans H Scheld; Wilhelm Haverkamp; Peter Milberg; Günter Breithardt; Eric Schulze-Bahr; Dirk Böcker
Implantable cardioverter-defibrillator therapy in patients with congenital long-QT syndrome: a long-term follow-up.
Heart rhythm : the official journal of the Heart Rhythm Society 2005;2(5):497-504.
2005: Eric Schulze-Bahr
Short QT syndrome or Andersen syndrome: Yin and Yang of Kir2.1 channel dysfunction.
Circulation research 2005;96(7):703-4.
2005: Charles Antzelevitch; Pedro Brugada; Martin Borggrefe; Josep Brugada; Ramon Brugada; Domenico Corrado; Ihor Gussak; Herve LeMarec; Koonlawee Nademanee; Andres Ricardo Perez Riera; Wataru Shimizu; Eric Schulze-Bahr; Hanno Tan; Arthur Wilde
Brugada syndrome: report of the second consensus conference.
Heart rhythm : the official journal of the Heart Rhythm Society 2005;2(4):429-40.
2005: Eric Schulze-Bahr; Günter Breithardt
Short QT interval and short QT syndromes.
Journal of cardiovascular electrophysiology 2005;16(4):397-8.
2005: Charles Antzelevitch; Pedro Brugada; Martin Borggrefe; Josep Brugada; Ramon Brugada; Domenico Corrado; Ihor Gussak; Herve LeMarec; Koonlawee Nademanee; Andres Ricardo Perez Riera; Wataru Shimizu; Eric Schulze-Bahr; Hanno Tan; Arthur Wilde
Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.
Circulation 2005;111(5):659-70.
2004: Paulus Kirchhof; Stephan Zellerhoff; Gerold Mönnig; Eric Schulze-Bahr
Pauses after burst pacing provoke afterdepolarizations and torsades de pointes in a patient with long QT syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2004;1(6):720-3.
2004: Peter Kies; Thomas Wichter; Michael Schäfers; Matthias Paul; Klaus P Schäfers; Lars Eckardt; Lars Stegger; Eric Schulze-Bahr; Ornella E Rimoldi; Günter Breithardt; Otmar Schober; Paolo G Camici
Abnormal myocardial presynaptic norepinephrine recycling in patients with Brugada syndrome.
Circulation 2004;110(19):3017-22.
2004: Brenda Gerull; Arnd Heuser; Thomas Wichter; Matthias Paul; Craig T Basson; Deborah McDermott; Bruce B Lerman; Steve M Markowitz; Patrick T Ellinor; Calum A MacRae; Stefan Peters; Katja S Grossmann; Jörg Drenckhahn; Beate Michely; Sabine Sasse-Klaassen; Walter Birchmeier; Rainer Dietz; Günter Breithardt; Eric Schulze-Bahr; Ludwig Thierfelder
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy.
Nature genetics 2004;36(11):1162-4.
2004: Stefan Kääb; Arne Pfeufer; Martin Hinterseer; Michael Näbauer; Eric Schulze-Bahr
Long QT syndrome. Why does sex matter?
Zeitschrift für Kardiologie 2004;93(9):641-5.
2004: Hans Gerd Kehl; Wilhelm Haverkamp; Georg Rellensmann; T Mesud Yelbuz; Thomas Krasemann; Johannes Vogt; Eric Schulze-Bahr
Images in cardiovascular medicine. Life-threatening neonatal arrhythmia: successful treatment and confirmation of clinically suspected extreme long QT-syndrome-3.
Circulation 2004;109(18):e205-6.
2004: Petra Ursula Seiler; Jörg Stypmann; Günter Breithardt; Eric Schulze-Bahr
Real-time RT-PCR for gene expression profiling in blood of heart failure patients-a pilot study: gene expression in blood of heart failure patients.
Basic research in cardiology 2004;99(3):230-8.
2004: Aimée D C Paulussen; Ron A H J Gilissen; Martin Armstrong; Pieter A Doevendans; Peter Verhasselt; H J M Smeets; Eric Schulze-Bahr; Wilhelm Haverkamp; Günter Breithardt; Nadine Cohen; Jeroen Aerssens
Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
Journal of molecular medicine (Berlin, Germany) 2004;82(3):182-8.
2004: Horst Wedekind; M Schwarz; S Hauenschild; H Djonlagic; Wilhelm Haverkamp; Günter Breithardt; T Wülfing; Olaf Pongs; Dirk Isbrandt; Eric Schulze-Bahr
Effective long-term control of cardiac events with beta-blockers in a family with a common LQT1 mutation.
Clinical genetics 2004;65(3):233-41.
2004: Carsten Müller-Tidow; Joachim Schwäble; Björn Steffen; Nicola Tidow; Burkhard Brandt; Kerstin Becker; Eric Schulze-Bahr; Hartmut Halfter; Ulf Vogt; Ralf Metzger; Paul M Schneider; Thomas Büchner; Christian Brandts; Wolfgang E Berdel; Hubert Serve
High-throughput analysis of genome-wide receptor tyrosine kinase expression in human cancers identifies potential novel drug targets.
Clinical cancer research : an official journal of the American Association for Cancer Research 2004;10(4):1241-9.
2004: Eric Schulze-Bahr; H Fenge; D Etzrodt; Wilhelm Haverkamp; Gerold Mönnig; Horst Wedekind; Günter Breithardt; Hans Gerd Kehl
Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response.
Heart (British Cardiac Society) 2004;90(1):13-6.
2003: Paulus Kirchhof; Eric Schulze-Bahr
Atrial fibrillation, thromboembolism, and haemostasis: causal or casual associations?
Thrombosis and haemostasis 2003;90(6):973-5.
2003: Paulus Kirchhof; Lars Eckardt; Michael R Franz; Gerold Mönnig; Peter Loh; Horst Wedekind; Eric Schulze-Bahr; Günter Breithardt; Wilhelm Haverkamp
Prolonged atrial action potential durations and polymorphic atrial tachyarrhythmias in patients with long QT syndrome.
Journal of cardiovascular electrophysiology 2003;14(10):1027-33.
2003: Eric Schulze-Bahr; Karl-Albert Zoelch; Lars Eckardt; Wilhelm Haverkamp; Günter Breithardt; Martin Borggrefe
Electrical alternans in long QT syndrome resembling a Brugada syndrome pattern.
Pacing and clinical electrophysiology : PACE 2003;26(10):2033-5.
2003: Eric Schulze-Bahr; Lars Eckardt; Günter Breithardt; Karlheinz Seidl; Thomas Wichter; Christian Wolpert; Martin Borggrefe; Wilhelm Haverkamp
Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease.
Human mutation 2003;21(6):651-2.
2003: Eric Schulze-Bahr; Axel Neu; Patrick Friederich; U Benjamin Kaupp; Günter Breithardt; Olaf Pongs; Dirk Isbrandt
Pacemaker channel dysfunction in a patient with sinus node disease.
The Journal of clinical investigation 2003;111(10):1537-45.
2003: Eric Schulze-Bahr; Gerold Mönnig; Lars Eckardt; Horst Wedekind; Thomas Wichter; Günter Breithardt
The long QT syndrome: considerations in the athletic population.
Current sports medicine reports 2003;2(2):72-8.
2003: Matthias Paul; Eric Schulze-Bahr; Günter Breithardt; Thomas Wichter
Genetics of arrhythmogenic right ventricular cardiomyopathy--status quo and future perspectives.
Zeitschrift für Kardiologie 2003;92(2):128-36.
2002: Thomas Wichter; Eric Schulze-Bahr; Lars Eckardt; Matthias Paul; Bodo Levkau; Matthias Meyborg; Michael Schäfers; Wilhelm Haverkamp; Günter Breithardt
Molecular mechanisms of inherited ventricular arrhythmias.
Herz 2002;27(8):712-39.
2002: Horst Wedekind; Eric Schulze-Bahr; H Djonlagic
Postextrasystolic "T wave hump" augmentation as a marker of increased arrhythmogenic risk in the long QT syndrome.
Heart (British Cardiac Society) 2002;88(6):633.
2002: Lars Eckardt; Paulus Kirchhof; Eric Schulze-Bahr; Sascha Rolf; Michael Ribbing; Peter Loh; Hans-Jürgen Bruns; A Witte; Peter Milberg; Martin Borggrefe; Günter Breithardt; Thomas Wichter; Wilhelm Haverkamp
Electrophysiologic investigation in Brugada syndrome; yield of programmed ventricular stimulation at two ventricular sites with up to three premature beats.
European heart journal 2002;23(17):1394-401.
2002: J Junker; Wilhelm Haverkamp; Eric Schulze-Bahr; Lars Eckardt; Werner Paulus; R Kiefer
Amiodarone and acetazolamide for the treatment of genetically confirmed severe Andersen syndrome.
Neurology 2002;59(3):466.
2002: Lars Eckardt; Hans-Jürgen Bruns; Matthias Paul; Paulus Kirchhof; Eric Schulze-Bahr; Thomas Wichter; Günter Breithardt; Martin Borggrefe; Wilhelm Haverkamp
Body surface area of ST elevation and the presence of late potentials correlate to the inducibility of ventricular tachyarrhythmias in Brugada syndrome.
Journal of cardiovascular electrophysiology 2002;13(8):742-9.
2002: Dirk Isbrandt; Patrick Friederich; Anna Solth; Wilhelm Haverkamp; Andreas Ebneth; Martin Borggrefe; Harald Funke; Kathrin Sauter; Günter Breithardt; Olaf Pongs; Eric Schulze-Bahr
Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics.
Journal of molecular medicine (Berlin, Germany) 2002;80(8):524-32.
2002: Jeroen P P Smits; Lars Eckardt; Vincent Probst; Connie R Bezzina; Jean-Jacques Schott; Carol Ann Remme; Wilhelm Haverkamp; Günter Breithardt; Denis Escande; Eric Schulze-Bahr; Herve LeMarec; Arthur A M Wilde
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.
Journal of the American College of Cardiology 2002;40(2):350-6.
2002: Gerold Mönnig; Eric Schulze-Bahr; Horst Wedekind; Lars Eckardt; Paulus Kirchhof; Harald Funke; S Kotthoff; J Vogt; G Assmann; G Breithardt; W Haverkamp
[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome].
Zeitschrift für Kardiologie 2002;91(5):380-8.
2002: Hans-Jürgen Bruns; Lars Eckardt; Christian Vahlhaus; Eric Schulze-Bahr; Wilhelm Haverkamp; Martin Borggrefe; Günter Breithardt; Thomas Wichter
Body surface potential mapping in patients with Brugada syndrome: right precordial ST segment variations and reverse changes in left precordial leads.
Cardiovascular research 2002;54(1):58-66.
2002: Wilhelm Haverkamp; Gerold Mönnig; Eric Schulze-Bahr; Franziska Haverkamp; Günter Breithardt
Physician-induced torsade de pointes--therapeutic implications.
Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy 2002;16(2):101-9.
2002: Thomas Wichter; Peter Matheja; Lars Eckardt; Peter Kies; Klaus P Schäfers; Eric Schulze-Bahr; Wilhelm Haverkamp; Martin Borggrefe; Otmar Schober; Günter Breithardt; Michael Schäfers
Cardiac autonomic dysfunction in Brugada syndrome.
Circulation 2002;105(6):702-6.
2001: Peter J Schwartz; silvia priori; Raffaella Bloise; Carlo Napolitano; Elena Ronchetti; A Piccinini; C Goj; G Breithardt; Eric Schulze-Bahr; Horst Wedekind; Janni Nastoli
Molecular diagnosis in a child with sudden infant death syndrome.
Lancet 2001;358(9290):1342-3.
2001: Horst Wedekind; Jeroen P P Smits; Eric Schulze-Bahr; R Arnold; Marieke W Veldkamp; Thomas Bajanowski; Martin Borggrefe; Bernd Brinkmann; I Warnecke; Harald Funke; Zahurul A Bhuiyan; Arthur A M Wilde; Günter Breithardt; Wilhelm Haverkamp
De novo mutation in the SCN5A gene associated with early onset of sudden infant death.
Circulation 2001;104(10):1158-64.
2001: Eric Schulze-Bahr; M Schwarz; S Hauenschild; Horst Wedekind; Harald Funke; Wilhelm Haverkamp; Günter Breithardt; Olaf Pongs; Dirk Isbrandt; S Hoffman
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype.
Journal of molecular medicine (Berlin, Germany) 2001;79(9):504-9.
2001: Lars Eckardt; Paulus Kirchhof; Peter Loh; Eric Schulze-Bahr; R Johna; Thomas Wichter; Günter Breithardt; Wilhelm Haverkamp; Martin Borggrefe
Brugada syndrome and supraventricular tachyarrhythmias: a novel association?
Journal of cardiovascular electrophysiology 2001;12(6):680-5.
2001: G Moennig; Eric Schulze-Bahr; Horst Wedekind; Martin Borggrefe; Harald Funke; M Toelle; Paulus Kirchhof; Lars Eckardt; Gerd Assmann; Günter Breithardt; Wilhelm Haverkamp
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome.
Pacing and clinical electrophysiology : PACE 2001;24(4 Pt 1):406-15.
2001: Peter J Schwartz; silvia priori; Carla Spazzolini; Arthur J Moss; G Michael Vincent; Carlo Napolitano; Isabelle Denjoy; P Guicheney; Günter Breithardt; Mark T Keating; J A Towbin; Alan H Beggs; Paul Brink; Arthur A M Wilde; Lauri Toivonen; W Zareba; J L Robinson; Katherine W Timothy; Valerie A Corfield; Duangrurdee Wattanasirichaigoon; C Corbett; W Haverkamp; Eric Schulze-Bahr; Michael H Lehmann; K Schwartz; P Coumel; Raffaella Bloise
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.
Circulation 2001;103(1):89-95.
2000: Paulus Kirchhof; Lars Eckardt; Gerold Mönnig; R Johna; Peter Loh; Eric Schulze-Bahr; Günter Breithardt; Martin Borggrefe; Wilhelm Haverkamp
A patient with "atrial torsades de pointes".
Journal of cardiovascular electrophysiology 2000;11(7):806-11.
2000: Wilhelm Haverkamp; Lars Eckardt; Paulus Kirchhof; Gerold Mönnig; Eric Schulze-Bahr; Horst Wedekind; Martin Borggrefe; Michael Madeja; Günter Breithardt
[New knowledge in arrhythmogenesis--role of ion channels and genetic aspects].
Zeitschrift für Kardiologie 2000;89 Suppl 10():2-9; discussion 9-10.
2000: Eric Schulze-Bahr; Wilhelm Haverkamp; Martin Borggrefe; Horst Wedekind; Gerold Mönnig; J Mergenthaler; Gerd Assmann; Harald Funke; Günter Breithardt
Molecular genetics of arrhythmias--a new paradigm.
Zeitschrift für Kardiologie 2000;89 Suppl 4():IV12-22.
1999: Wilhelm Haverkamp; Eric Schulze-Bahr; Gerold Mönnig; Horst Wedekind; Martin Borggrefe; Harald Funke; Günter Breithardt
[Congenital and "acquired QT syndromes].
Herz 1999;24(7):587-90.
1999: C Rubie; Eric Schulze-Bahr; Horst Wedekind; Martin Borggrefe; Wilhelm Haverkamp; Günter Breithardt
Multistep-touchdown vectorette-PCR--a rapid technique for the identification of IVS in genes.
BioTechniques 1999;27(3):414-6, 418.
1999: Wilhelm Haverkamp; Gerold Mönnig; Horst Wedekind; Eric Schulze-Bahr; Martin Borggrefe; Gerd Assmann; Harald Funke; Günter Breithardt
[Clinical aspects and molecular genetics of the long QT-syndrome].
Deutsche medizinische Wochenschrift (1946) 1999;124(33):972-9.
1999: Eric Schulze-Bahr; Horst Wedekind; Wilhelm Haverkamp; Martin Borggrefe; Gerd Assmann; Günter Breithardt; Harald Funke
The LQT syndromes--current status of molecular mechanisms.
Zeitschrift für Kardiologie 1999;88(4):245-54.
1999: Myriam Berthet; Isabelle Denjoy; C Donger; L Demay; H Hammoude; Didier Klug; Eric Schulze-Bahr; Pascale Richard; H Funke; Ketty Schwartz; Philippe Coumel; Bernard Hainque; Pascale Guicheney
C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
Circulation 1999;99(11):1464-70.
1997: Eric Schulze-Bahr; Q Wang; Horst Wedekind; Wilhelm Haverkamp; Q Chen; Y Sun; C Rubie; M Hördt; J A Towbin; Martin Borggrefe; Gerd Assmann; X Qu; J C Somberg; Günter Breithardt; C Oberti; Harald Funke
KCNE1 mutations cause jervell and Lange-Nielsen syndrome.
Nature genetics 1997;17(3):267-8.
1997: Eric Schulze-Bahr; Wilhelm Haverkamp; Horst Wedekind; C Rubie; M Hördt; Martin Borggrefe; Gerd Assmann; Günter Breithardt; Harald Funke
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous.
Human genetics 1997;100(5-6):573-6.
1996: Eric Schulze-Bahr; Wilhelm Haverkamp; Günter Breithardt; Harald Funke; Heiko Wiebusch; Gerd Assmann
ECG repolarization patterns in chromosome 7-linked QT syndrome (LQTS 2)
Circulation 1996;94(9):2318-9.
1995: Eric Schulze-Bahr; Wilhelm Haverkamp; Harald Funke
The long-QT syndrome.
The New England journal of medicine 1995;333(26):1783-4.
1995: Eric Schulze-Bahr; Wilhelm Haverkamp; Heiko Wiebusch; Helmut Schulte; M Hördt; Martin Borggrefe; Günter Breithardt; Gerd Assmann; Harald Funke
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndrome.
Journal of molecular medicine (Berlin, Germany) 1995;73(11):565-9.