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Heart (British Cardiac Society)|August 17, 2005
Predictors of adverse outcome in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy: long term experience of a tertiary care centreK Lemola, C Brunckhorst, U Helfenstein, et al.Heart (British Cardiac Society)|November 17, 2001
Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathyR Jenni, E Oechslin, J Schneider, et al.Therapeutische Umschau. Revue Therapeutique|November 5, 1999
[Cardiovascular disease in pregnancy]E Oechslin, J Turina, U Lauper, et al.Cardiology|July 15, 2000
Extensive thrombus formation in the right ventricle due to a rare combination of arrhythmogenic right ventricular cardiomyopathy and heterozygous prothrombin gene mutation G20210 AC H Attenhofer Jost, T Bombeli, C Schrimpf, et al.British Heart Journal|December 1, 1995
Pseudoaneurysm following aortic homograft: clinical implications?E Oechslin, T Carrel, M Ritter, et al.Therapeutische Umschau. Revue Therapeutique|August 1, 1996
[Treatment strategies in mechanical and electrical cardiovascular failure]E OechslinHeart (British Cardiac Society)|February 18, 2004
Aberrant tendinous chords with tethering of the tricuspid leaflets: a congenital anomaly causing severe tricuspid regurgitationR Kobza, D J Kurz, E N Oechslin, et al.Therapeutische Umschau. Revue Therapeutique|March 10, 2001
[Organizational and medical aspects of transition of juveniles with congenital heart defects to adult cardiology care]E Oechslin, A HoffmannSchweizerische Medizinische Wochenschrift|August 31, 1985
[Hashimoto's lymphomatous thyroiditis and endemic struma]E Oechslin, C HedingerPageof 44