Keller DI - Search Results

1

A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation.

Keller DI, Huang H, Zhao J, Frank R, Suarez V, Delacrétaz E, Brink M, Osswald S, Schwick N, Chahine M. Keller DI, et al. Cardiovasc Res. 2006 Jun 1;70(3):521-9. doi: 10.1016/j.cardiores.2006.02.030. Epub 2006 Mar 3. Cardiovasc Res. 2006. PMID: 16616735 Free article.

2

Rate response of a closed-loop stimulation pacing system to changing preload and afterload conditions.

Cron TA, Pouskoulas CD, Keller DI, Zaugg CE, Buser PT, Pfisterer ME, Osswald S, Hilti P, Schächinger H. Cron TA, et al. Among authors: keller di. Pacing Clin Electrophysiol. 2003 Jul;26(7 Pt 1):1504-10. doi: 10.1046/j.1460-9592.2003.t01-1-00218.x. Pacing Clin Electrophysiol. 2003. PMID: 12914629

3

A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.

Keller DI, Acharfi S, Delacrétaz E, Benammar N, Rotter M, Pfammatter JP, Fressart V, Guicheney P, Chahine M. Keller DI, et al. J Mol Cell Cardiol. 2003 Dec;35(12):1513-21. doi: 10.1016/j.yjmcc.2003.08.007. J Mol Cell Cardiol. 2003. PMID: 14654377

4

Arrhythmogenic right ventricular cardiomyopathy: diagnostic and prognostic value of the cardiac MRI in relation to arrhythmia-free survival.

Keller DI, Osswald S, Bremerich J, Bongartz G, Cron TA, Hilti P, Pfisterer ME, Buser PT. Keller DI, et al. Int J Cardiovasc Imaging. 2003 Dec;19(6):537-43; discussion 545-7. doi: 10.1023/b:caim.0000004351.40409.ee. Int J Cardiovasc Imaging. 2003. PMID: 14690194

5

Brugada syndrome and fever: genetic and molecular characterization of patients carrying SCN5A mutations.

Keller DI, Rougier JS, Kucera JP, Benammar N, Fressart V, Guicheney P, Madle A, Fromer M, Schläpfer J, Abriel H. Keller DI, et al. Cardiovasc Res. 2005 Aug 15;67(3):510-9. doi: 10.1016/j.cardiores.2005.03.024. Cardiovasc Res. 2005. PMID: 15890323 Free article.

6

A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state.

Keller DI, Barrane FZ, Gouas L, Martin J, Pilote S, Suarez V, Osswald S, Brink M, Guicheney P, Schwick N, Chahine M. Keller DI, et al. Can J Cardiol. 2005 Sep;21(11):925-31. Can J Cardiol. 2005. PMID: 16239976

7

Value of repeated cardiac magnetic resonance imaging in patients with suspected arrhythmogenic right ventricular cardiomyopathy.

Conen D, Osswald S, Cron TA, Linka A, Bremerich J, Keller DI, Pfisterer ME, Buser PT. Conen D, et al. Among authors: keller di. J Cardiovasc Magn Reson. 2006;8(2):361-6. doi: 10.1080/10976640500527082. J Cardiovasc Magn Reson. 2006. PMID: 16669179

8

Brugada syndrome unmasked by accidental inhalation of gasoline vapors.

Kranjcec D, Bergovec M, Rougier JS, Raguz M, Pavlovic S, Jespersen T, Castella V, Keller DI, Abriel H. Kranjcec D, et al. Among authors: keller di. Pacing Clin Electrophysiol. 2007 Oct;30(10):1294-8. doi: 10.1111/j.1540-8159.2007.00857.x. Pacing Clin Electrophysiol. 2007. PMID: 17897138

9

Analyses of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome.

Petitprez S, Jespersen T, Pruvot E, Keller DI, Corbaz C, Schläpfer J, Abriel H, Kucera JP. Petitprez S, et al. Among authors: keller di. Cardiovasc Res. 2008 Jun 1;78(3):494-504. doi: 10.1093/cvr/cvn023. Epub 2008 Feb 5. Cardiovasc Res. 2008. PMID: 18252757

10

Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures.

Keller DI, Grenier J, Christé G, Dubouloz F, Osswald S, Brink M, Ficker E, Chahine M. Keller DI, et al. Can J Cardiol. 2009 Aug;25(8):455-62. doi: 10.1016/s0828-282x(09)70117-5. Can J Cardiol. 2009. PMID: 19668779 Free PMC article.

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