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	1.	Cardiovascular disease and sudden cardiac death: between genetics and genomics. [electronic resource] by Stallmeyer, Birgit Schulze-Bahr, Eric Producer: 20160405 In: European heart journal vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Identification of novel mutations in LMNA associated with familial forms of dilated cardiomyopathy. [electronic resource] by Stallmeyer, Birgit Koopmann, Matthias Schulze-Bahr, Eric Producer: 20121022 In: Genetic testing and molecular biomarkers vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	(Tpeak - Tend)/QRS and (Tpeak - Tend)/(QT × QRS) as risk markers in Brugada syndrome: authors' reply. [electronic resource] by Zumhagen, Sven Stallmeyer, Birgit Eckardt, Lars Schulze-Bahr, Eric Producer: 20180423 In: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Regulation of eNOS in normal and diabetes-impaired skin repair: implications for tissue regeneration. [electronic resource] by Stallmeyer, Birgit Anhold, Manuel Wetzler, Christian Kahlina, Kornelija Pfeilschifter, Josef Frank, Stefan Producer: 20020619 In: Nitric oxide : biology and chemistry vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genes causing inherited forms of cardiomyopathies. A current compendium. [electronic resource] by Paul, Matthias Zumhagen, Sven Stallmeyer, Birgit Koopmann, Matthias Spieker, Tilmann Schulze-Bahr, Eric Producer: 20090706 In: Herz vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy. [electronic resource] by Zumhagen, Sven Stallmeyer, Birgit Friedrich, Corinna Eckardt, Lars Seebohm, Guiscard Schulze-Bahr, Eric Producer: 20130401 In: Herzschrittmachertherapie & Elektrophysiologie vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Tpeak-Tend interval and Tpeak-Tend/QT ratio in patients with Brugada syndrome. [electronic resource] by Zumhagen, Sven Zeidler, Eva Maria Stallmeyer, Birgit Ernsting, Marko Eckardt, Lars Schulze-Bahr, Eric Producer: 20170816 In: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease. [electronic resource] by Neu, Axel Eiselt, Michele Paul, Matthias Sauter, Kathrin Stallmeyer, Birgit Isbrandt, Dirk Schulze-Bahr, Eric Producer: 20101020 In: Human mutation vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	PKC delta-induced activation of MAPK pathway is required for bFGF-stimulated proliferation of coronary smooth muscle cells. [electronic resource] by Skaletz-Rorowski, Adriane Eschert, Heike Leng, Jutta Stallmeyer, Birgit Sindermann, Jürgen R Pulawski, Ewa Breithardt, Günter Producer: 20051213 In: Cardiovascular research vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correction. [electronic resource] by Malan, Daniela Zhang, Miao Stallmeyer, Birgit Müller, Jovanca Fleischmann, Bernd K Schulze-Bahr, Eric Sasse, Philipp Greber, Boris Producer: 20161021 In: Basic research in cardiology vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channel. [electronic resource] by Henrion, Ulrike Zumhagen, Sven Steinke, Katja Strutz-Seebohm, Nathalie Stallmeyer, Birgit Lang, Florian Schulze-Bahr, Eric Seebohm, Guiscard Producer: 20121108 In: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder. [electronic resource] by Friedrich, Corinna Rinné, Susanne Zumhagen, Sven Kiper, Aytug K Silbernagel, Nicole Netter, Michael F Stallmeyer, Birgit Schulze-Bahr, Eric Decher, Niels Producer: 20150209 In: EMBO molecular medicine vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Structural interplay of K [electronic resource] by Rothenberg, Ina Piccini, Ilaria Wrobel, Eva Stallmeyer, Birgit Müller, Jovanca Greber, Boris Strutz-Seebohm, Nathalie Schulze-Bahr, Eric Schmitt, Nicole Seebohm, Guiscard Publication details: HeartRhythm case reports Nov 2016 In: HeartRhythm case reports vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I. [electronic resource] by Kruse, Martin Schulze-Bahr, Eric Corfield, Valerie Beckmann, Alf Stallmeyer, Birgit Kurtbay, Güven Ohmert, Iris Schulze-Bahr, Ellen Brink, Paul Pongs, Olaf Producer: 20091002 In: The Journal of clinical investigation vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K [electronic resource] by Kuß, Johanna Stallmeyer, Birgit Goldstein, Matthias Rinné, Susanne Pees, Christiane Zumhagen, Sven Seebohm, Guiscard Decher, Niels Pott, Lutz Kienitz, Marie-Cécile Schulze-Bahr, Eric Producer: 20200312 In: Circulation. Genomic and precision medicine vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome. [electronic resource] by Zumhagen, Sven Veldkamp, Marieke W Stallmeyer, Birgit Baartscheer, Antonius Eckardt, Lars Paul, Matthias Remme, Carol Ann Bhuiyan, Zahurul A Bezzina, Connie R Schulze-Bahr, Eric Producer: 20140424 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype. [electronic resource] by Limberg, Maren M Zumhagen, Sven Netter, Michael F Coffey, Alison J Grace, Andrew Rogers, Jane Böckelmann, Doris Rinné, Susanne Stallmeyer, Birgit Decher, Niels Schulze-Bahr, Eric Producer: 20130816 In: Basic research in cardiology vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography. [electronic resource] by Zumhagen, Sven Vrachimis, Alexis Stegger, Lars Kies, Peter Wenning, Christian Ernsting, Marko Müller, Jovanca Seebohm, Guiscard Paul, Matthias Schäfers, Klaus Stallmeyer, Birgit Schäfers, Michael Schulze-Bahr, Eric Producer: 20181114 In: Heart (British Cardiac Society) vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbances. [electronic resource] by Stallmeyer, Birgit Zumhagen, Sven Denjoy, Isabelle Duthoit, Guillaume Hébert, Jean-Louis Ferrer, Xavier Maugenre, Svetlana Schmitz, Wilhelm Kirchhefer, Uwe Schulze-Bahr, Ellen Guicheney, Pascale Schulze-Bahr, Eric Producer: 20120423 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome. [electronic resource] by Wemhöner, Konstantin Friedrich, Corinna Stallmeyer, Birgit Coffey, Alison J Grace, Andrew Zumhagen, Sven Seebohm, Guiscard Ortiz-Bonnin, Beatriz Rinné, Susanne Sachse, Frank B Schulze-Bahr, Eric Decher, Niels Producer: 20151120 In: Journal of molecular and cellular cardiology vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 31 results.