Auswahl an Publikationen von PD Horst Wedekind
Wedekind H, Özgün M. Prolonged reversible cortical blindness over 5 days after cardiac catheterization. Med Klin Intensivmed Notfmed. 2017;112:535-539.
Wedekind H, Rozhnev A, Kleine-Katthöfer P, Kranig W. Epileptic seizure in a patient with an implantable cardioverter-defibrillator: Quo vadis right ventricular lead? Herzschrittmacherther Elektrophysiol. 2016;27:63-6.
Böhm M, Mahfoud F, Ukena C, Hoppe UC, Narkiewicz K, Negoita M, Ruilope L, Schlaich MP, Schmieder RE, Whitbourn R, Williams B, Zeymer U, Zirlik A, Mancia G; GSR Investigators. First report of the Global SYMPLICITY Registry on the effect of renal artery denervation in patients with uncontrolled hypertension. Hypertension. 2015;65:766-74.
Wedekind H, Grossekettler U, Matheja P, Kleine-Katthoefer P. PET-CT imaging in the diagnosis of coronary stent infection. J Nucl Cardiol. 2013;20:1184-5.
Giant left atrial sarcoma. Wedekind H, Koesek V, Welp H, Scheld HH. J Card Surg. 2013;28:705-6.
Schmitt M, Wichmann A, Wedekind H. 86-year-old patient with left thoracic, breathing-dependent pain. Dtsch Med Wochenschr. 2012;137:533-4.
Wedekind H, Böcker D, Scheld HH, Zörner D. Dual chamber pacemaker implantation in a patient with persistent left superior vena cava after orthotopic heart transplantation. Wien Klin Wochenschr. 2010;122:22.
Wedekind H, Müller JG, Ribbing M, Skurzewski P, Bozzetti C, Meyer-Krahmer HJ, Böcker D. A fatal combination in an old lady: Tako-Tsubo cardiomyopathy, long QT syndrome, and cardiac hypertrophy. Europace. 2009;11:820-2.
Wedekind H, Burde D, Zumhagen S, Debus V, Burkhardtsmaier G Mönnig G, Breithardt G, Schulze-Bahr E. QT interval prolongation and risk for cardiac events in genotyped LQTS index children. Eur J Pediatr. Eur J Pediatr. 2009;168:1107-15.
Böcker D, Wedekind H. Defibrillator-Therapie: eine fallorientierte Darstellung. Kardiologie up2date. 2007;3:123-134.
Wedekind H, Müller JG. Visual diagnosis in cardiology: Malposition of dual chamber pacemaker lead. Anaesth Intensive Care 2007;35:806.
Wedekind H, Moller K. Pulmonary fluid status monitoring system for terminal heart failure. Dtsch Med Wochenschr 2007;132:555-559.
Wedekind H, Schulze-Bahr E, Debus V, Breithardt G, Brinkmann B, Bajanowski T. Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigation. Int J Legal Med 2007;121:245-257.
Monnig G, Eckardt L, Wedekind H, Haverkamp W, Gerss J, Milberg P, Wasmer K, Kirchhof P, Assmann G, Breithardt G, Schulze-Bahr E. Electrocardiographic risk stratification in families with congenital long QT syndrome. Eur Heart J 2006;17:2074-2080.
Wedekind H, Moller K, Scholz KH. Giant thrombus trapped in foramen ovale with paradoxical cerebral embolization and stroke. Clin Cardiol 2006;10:466.
Wedekind H, Möller K, Scholz KH. Tako-Tsubo Kardiomyopathie - Inzidenz bei Patienten mit akutem Koronarsyndrom. Herz 2006;31:339-346.
Gradaus R, Eckardt L, Wedekind H, Loher A, Bocker D. Transvenous ICD implantation after artificial tricuspid valve replacement. A new approach placing a transvenous ICD lead in the mid cardiac vein of the coronary sinus. Z Kardiol 2005;94:588-591.
Smits JP, Veldkamp MW, Bezzina CR, Bhuiyan ZA, Wedekind H, Schulze-Bahr E, Wilde AA. Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome. Cardiovasc Res 2005;3:459-466.
Monnig G, Kobe J, Loher A, Eckardt L, Wedekind H, Scheld HH, Haverkamp W, Milberg P, Breithardt G, Schulze-Bahr E, Bocker D. Implantable cardioverter-defibrillator therapy in patients with congenital long-QT syndrome: A long-term follow-up. Heart Rhythm 2005;2:497-504.
Wedekind H, Bajanowski T, Friederich P, Breithardt G, Wülfing T, Siebrands C, Engeland B, Mönnig G, Haverkamp W, Brinkmann B, Schulze-Bahr E. Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study. Int J Legal Med 2005;120:129-137.
Wedekind H, Gradaus R, Loeher A, Böcker D. Combined P/S-HV ICD lead implantation via the coronary sinus in a patient with a prosthetic tricuspid valve. J Cardiovasc Electrophysiol 2005;16:1-2.
Wedekind H, Schwarz M, Hauenschild S, Djonlagic H, Haverkamp W, Breithardt G, Wulfing T, Pongs O, Isbrandt D, Schulze-Bahr E. Effective long-term control of cardiac events with beta-blockers in a family with a common LQT1 mutation. Clin Genet 2004;65:233-241.
Acil T, Schulze-Bahr E, Wichter T, Breithardt G, Wedekind H. Sudden cardiac death and genetics. Turkish Journal of Arrhythmia, Pacing and Electrophysiology 2004;2:17-30.
Schulze-Bahr E, Fenge H, Etzrodt D, Haverkamp W, Monnig G, Wedekind H, Breithardt G, Kehl HG. Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response. Heart 2004;90:13-16.
Schulze Bahr E, Mönnig G, Eckardt L, Wedekind H, Wichter T, Breithardt G. The long QT syndrome: Considerations in the athletic population. Current Sports Medicine Reports 2003;2:72-78.
Bajanowski T, Ortmann C, Teige K, Wedekind H, Zack F, Rose I, Brinkmann B. Pathological changes of the heart in sudden infant death. Int J Legal Med 2003;117:193-203.
Kirchhof P, Eckardt L, Franz MR, Mönnig G, Loh P, Wedekind H, Schulze-Bahr E, Breithardt G, Haverkamp W. Prolonged atrial action potential durations and polymorphic atrial tachyarrhythmias in patients with long QT syndrome. J Cardiovasc Electrophysiol 2003; 14:1027-1033.
Wedekind H, Mönnig G, Breithardt G, Schulze-Bahr E. Der plötzliche Herztod: Genetische Prädispositionen. Herzschr Elektrophysiol 2003;4:180-191
Wedekind H, Schulze-Bahr E, Djonlagic H. Postextrasystolic "T wave hump" augmentation as a marker of increased arrhythmogenic risk in the long QT syndrome. Heart 2002;88:633.
Wedekind H, Bisping G, Attaie T, Wessling J, Tombach B, Breithardt G, Domschke W. Differential diagnosis of dysphagia in an old lady. Clin Cardiol 2002;25:132.
Wedekind H, Smits JPP, Schulze-Bahr E, Arnold R, Veldkamp MW, Bajanowski T, Borggrefe M, Brinkmann B, Warnecke I, Funke H, Bhuiyan ZA, Wilde AAM, Breithardt G, Haverkamp W. De novo mutation in the SCN5A gene associated with early onset of sudden infant death. Circulation 2001;104:1158-1164.
Schulze-Bahr E, Schwarz M, Hoffmann S, Wedekind H, Funke H, Haverkamp W, Breithardt G, Pongs O, Isbrandt D. A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype. J Mol Med 2001;79:504-509.
Schwartz PJ, Priori SG, Bloise R, Napolitano C, Ronchetti E, Piccinini A, Goj C, Breithardt G, Schulze-Bahr E, Wedekind H, Nastoli J. Molecular diagnosis in a child with sudden infant death syndrome. Lancet 2001;358:1342-1343.
Haverkamp W, Mönnig G, Schulze-Bahr E, Wedekind H, Breithardt G. Kongenitale QT-Syndrome. Forum Rhythmologie 2001;4:16-20.
Bajanowski T, Rossi L, Biondo B, Ortmann C, Haverkamp W, Wedekind H, Jorch G, Brinkmann B. Prolonged QT interval and sudden infant death – report of two cases. Forensic Sci Int 2001;115:147-153.
Moennig G, Schulze-Bahr E, Wedekind H, Borggrefe M, Funke H, Toelle M, Kirchhof P, Eckardt L, Assmann G, Breithardt G, Haverkamp W. Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome. Pacing Clin Electrophysiol 2001;24:406-415.
Wedekind H, Schulze-Bahr E, FunkE H, Breithardt G, Haverkamp W, Borggrefe M. Long-QT-Syndrom – eine Ionenkanalerkrankung. Medizinische Genetik 1999;11:271-274.
Schulze-Bahr E, Haverkamp W, Wedekind H, Rubie C, Hördt M, Borggrefe M, Assmann G, Breithardt G, Funke H. Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous. Human Genet 1997;100:573-576.
Schulze-Bahr E, Wang Q, Wedekind H, Haverkamp W, Chen Q, Sun Y, Rubie C, Hördt M, Towbin J, Borggrefe M, Assmann G, Qu X, Somberg J C, Breithardt G, Oberti C, Funke H. KCNE1 mutations cause Jervell and Lange-Nielsen syndrome. Nature Genet 1997;17:267-268.
Schulze-Bahr E, Haverkamp W, Wiebusch H, Wedekind H, Assmann G, Breithardt G, Funke H. Molekulare Differenzierung des Romano-Ward-Syndroms. Herzschr Elektrophys 1996;7 (Suppl. 1): 21-26.
Hildebrandt F, Singh-Sawhney I, Schnieders B, Centofante L, Omran H, Pohlmann A, Schmaltz C, Wedekind H, Schubotz C, Antignac C, Weber L J, Brandis M. Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining the flanking markers on chromosome 2. Am J Hum Genet 1993;53:1256-1261.