Browse by Basel Contributors ID

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Ajdler-Schäffler, Evelyne and Kaplan, V. and Keller, D. I.. (2011) [Perioperative cardiac risk management]. Schweizerische Rundschau für Medizin PRAXIS, Vol. 100 , S. 687-696, quiz 695.

Stanek, Nadine and Keller, Dagmar I.. (2011) [Lack of blood pressure rise and blood pressure fall during ergometry]. Schweizerische Rundschau für Medizin PRAXIS, Vol. 100, H. 13 , S. 755-764, quiz 763.

Tomaske, Maren and Keller, Dagmar I. and Bauersfeld, Urs. (2011) Sudden cardiac death : clinical evaluation of paediatric family members. Europace, Vol. 13, H. 3. pp. 421-426.

Rüdiger-Stürchler, Marjam and Keller, Dagmar I. and Bingisser, Roland. (2010) Emergency physician intershift handover - can a dINAMO checklist speed it up and improve quality? Swiss Medical Weekly, Vol. 140 , w13085.

Nickel, C. H. and Stephan, F. P. and Dangel, M. and Blume, K. and Gehrisch, R. and Dumoulin, A. and Tschudin, S. and Keller, D. I. and Hirsch, H. H. and Widmer, A. F. and Bingisser, R.. (2009) First wave of the influenza A/H1N1v pandemic in Switzerland. Swiss medical weekly : official journal of the Swiss Society of Infectious Diseases, the Swiss Society of Internal Medicine, the Swiss Society of Pneumology, Vol. 139. pp. 731-737.

Keller, Dagmar I. and Grenier, Julie and Christé, Georges and Dubouloz, Frédérique and Osswald, Stefan and Brink, Marijke and Ficker, Eckhard and Chahine, Mohamed. (2009) Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures. The Canadian journal of cardiology = Journal canadien de cardiologie, Vol. 25. pp. 455-462.

Keller, D. I. and Schwitter, J. and Valsangiacomo, E. R. and Landolt, P. and Attenhofer Jost, C. H.. (2009) Hypertrophic cardiomyopathy due to beta-myosin heavy chain mutation with extreme phenotypic variability within a family. International journal of cardiology, Vol. 134, H. 3 , e87-93.

Petitprez, S. and Jespersen, T. and Pruvot, E. and Keller, D. I. and Corbaz, C. and Schläpfer, J. and Abriel, H. and Kucera, J. P.. (2008) Analyses of a novel SCN5A mutation (C1850S) : conduction vs : repolarization disorder hypotheses in the Brugada syndrome. Cardiovascular Research, Vol. 78. pp. 494-504.