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Zumhagen, S.
29  results:
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1

Whole exome sequencing (WES) in a patient with a cardiac co..:

Friedrich, C. ; Rinne, S. ; Zumhagen, S....
European Heart Journal.  34 (2013)  suppl 1 - p. P2296-P2296 , 2013
Link: https://doi.org/10.1093/..
 
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2

Prediction of variant pathogenicity in congenital LQT syndr..:

Stallmeyer, B. ; Schlegelberger, T. ; Zumhagen, S....
European Heart Journal.  34 (2013)  suppl 1 - p. P2302-P2302 , 2013
Link: https://doi.org/10.1093/..
 
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3

EKG-Quiz:

Bauersachs, J. ; Borggrefe, M. ; Eckardt, L....
Herzschrittmachertherapie + Elektrophysiologie.  23 (2012)  3 - p. 237-257 , 2012
Link: https://doi.org/10.1007/..
 
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4

Role of implantable cardioverter defibrillator therapy in p..:

Monnig, G. ; Kobe, J. ; Loher, A....
Europace.  14 (2011)  3 - p. 396-401 , 2011
Link: https://doi.org/10.1093/..
 
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5

Komplett subkutaner Kardioverter-Defibrillator (S-ICD®): Ak..:

Köbe, J. ; Zumhagen, S. ; Reinke, F...
Herz.  36 (2011)  7 - p. 586-591 , 2011
Link: https://doi.org/10.1007/..
 
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6

Brugada‐like cardiac disease in myotonic dystrophy type 2: ..:

Rudnik‐Schöneborn, S. ; Schaupp, M. ; Lindner, A....
European Journal of Neurology.  18 (2010)  1 - p. 191-194 , 2010
Link: https://doi.org/10.1111/..
 
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7

QT interval prolongation and risk for cardiac events in gen..:

Wedekind, H. ; Burde, D. ; Zumhagen, S....
European Journal of Pediatrics.  168 (2008)  9 - p. 1107-1115 , 2008
Link: https://doi.org/10.1007/..
 
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8

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh R ; Lahrouchi N ; Tadros R...
info:eu-repo/semantics/altIdentifier/pmid/32893267.  , 2021
Link: http://hdl.handle.net/23..
 
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9

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-020-00946-5.  , 2021
Link: https://inserm.hal.scien..
 
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10

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-020-00946-5.  , 2021
Link: https://inserm.hal.scien..
 
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11

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-020-00946-5.  , 2021
Link: https://inserm.hal.scien..
 
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12

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
https://openaccess.sgul.ac.uk/id/eprint/112371/3/s41436-020-00946-5.pdf.  , 2021
Link: https://openaccess.sgul...
 
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13

POPDC2 a novel susceptibility gene for conduction disorders:

Rinné S ; Ortiz-Bonnin B ; Stallmeyer B...
info:eu-repo/semantics/altIdentifier/pmid/32535041.  , 2020
Link: http://hdl.handle.net/11..
 
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14

Transethnic Genome-Wide Association Study Provides Insights..:

Lahrouchi, N ; Tadros, R ; Crotti, L...
https://openaccess.sgul.ac.uk/id/eprint/111978/12/CIRCULATIONAHA.120.045956.pdf.  , 2020
Link: https://openaccess.sgul...
 
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15

Transethnic genome-wide association study provides insights..:

Lahrouchi N ; Tadros R ; Crotti L...
info:eu-repo/semantics/altIdentifier/pmid/32429735.  , 2020
Link: http://hdl.handle.net/10..
 
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