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	1.	[Genetics of atrial fibrillation: rare mutations, common variants and clinical relevance?]. [electronic resource] by Sinner, M F Pfeufer, A Kääb, S Producer: 20060905 In: Herzschrittmachertherapie & Elektrophysiologie vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Differential modulation of human immunoglobulin isotype production by the neuropeptides substance P, NKA and NKB. [electronic resource] by Braun, A Wiebe, P Pfeufer, A Gessner, R Renz, H Producer: 19990712 In: Journal of neuroimmunology vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Long QT syndrome. Why does sex matter? [electronic resource] by Kääb, S Pfeufer, A Hinterseer, M Näbauer, M Schulze-Bahr, E Producer: 20041210 In: Zeitschrift fur Kardiologie vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Cost-Effectiveness Analysis of Ugt1a1 Genotyping Before Colorectal Cancer Treatment with Irinotecan. [electronic resource] by Butzke, B Oduncu, F Heinemann, V Pfeufer, A Giessen, C Stollenwerk, B Rogowski, W Producer: 20160610 In: Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	INSIG2 promoter variant, obesity markers and lipid parameters - No association in a large Slavonic Caucasian population sample. [electronic resource] by Hubácek, J A Kuthanová, L Bohuslavová, R Adámková, V Lánská, V Meitinger, T Pfeufer, A Producer: 20101103 In: Folia biologica vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	6.	Acute respiratory distress syndrome with transiently impaired left ventricular function and Torsades de Pointes arrhythmia unmasking congenital long QT syndrome in a 25-yr-old woman. [electronic resource] by Hinterseer, M Irlbeck, M Ney, L Beckmann, B-M Pfeufer, A Steinbeck, G Kaab, S Producer: 20060821 In: British journal of anaesthesia vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Angiotensin-converting enzyme and heart chymase gene polymorphisms in hypertrophic cardiomyopathy. [electronic resource] by Pfeufer, A Osterziel, K J Urata, H Borck, G Schuster, H Wienker, T Dietz, R Luft, F C Producer: 19960917 In: The American journal of cardiology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity. [electronic resource] by Yang, P Koopmann, T T Pfeufer, A Jalilzadeh, S Schulze-Bahr, E Kääb, S Wilde, A A Roden, D M Bezzina, C R Producer: 20080604 In: European journal of human genetics : EJHG vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21. [electronic resource] by Grohmann, K Wienker, T F Saar, K Rudnik-Schöneborn, S Stoltenburg-Didinger, G Rossi, R Novelli, G Nürnberg, G Pfeufer, A Wirth, B Reis, A Zerres, K Hübner, C Producer: 19991210 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Chymase gene locus is not associated with myocardial infarction and is not linked to heart size or blood pressure. [electronic resource] by Pfeufer, A Busjahn, A Vergopoulos, A Knoblauch, H Urata, H Osterziel, K J Menz, M Wienker, T F Faulhaber, H D Steinmetz, A Schuster, H Dietz, R Luft, F C Producer: 19981106 In: The American journal of cardiology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1. [electronic resource] by Grohmann, K Schuelke, M Diers, A Hoffmann, K Lucke, B Adams, C Bertini, E Leonhardt-Horti, H Muntoni, F Ouvrier, R Pfeufer, A Rossi, R Van Maldergem, L Wilmshurst, J M Wienker, T F Sendtner, M Rudnik-Schöneborn, S Zerres, K Hübner, C Producer: 20010927 In: Nature genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)