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	1.	[Analgesia in intensive care medicine]. [electronic resource] by Ortlepp, J R Luethje, F Walz, R Producer: 20170315 In: Medizinische Klinik, Intensivmedizin und Notfallmedizin vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Polymorphisms--genetic risk factors for coronary heart disease?]. [electronic resource] by Ortlepp, J R Klues, H G Hanrath, P Producer: 19990615 In: Deutsche medizinische Wochenschrift (1946) vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Lack of association among five genetic polymorphisms of the renin-angiotensin system and cardiac hypertrophy in patients with aortic stenosis. [electronic resource] by Ortlepp, J R Breithardt, O Ohme, F Hanrath, P Hoffmann, R Producer: 20010517 In: American heart journal vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Cardiovascular risk factors in patients with aortic stenosis predict prevalence of coronary artery disease but not of aortic stenosis: an angiographic pair matched case-control study. [electronic resource] by Ortlepp, J R Schmitz, F Bozoglu, T Hanrath, P Hoffmann, R Producer: 20030923 In: Heart (British Cardiac Society) vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Vitamin D receptor gene polymorphism BsmI is not associated with the prevalence and severity of CAD in a large-scale angiographic cohort of 3441 patients. [electronic resource] by Ortlepp, J R von Korff, A Hanrath, P Zerres, K Hoffmann, R Producer: 20030606 In: European journal of clinical investigation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	The vitamin D receptor gene variant is associated with the prevalence of type 2 diabetes mellitus and coronary artery disease. [electronic resource] by Ortlepp, J R Lauscher, J Hoffmann, R Hanrath, P Joost, H G Producer: 20020111 In: Diabetic medicine : a journal of the British Diabetic Association vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	[Prevalence and severity of pulmonary embolism are dependent on clinical and paraclinical parameters : Analysis of 1,943 consecutive patients with CT pulmonary angiography]. [electronic resource] by Kocea, P Mischke, K Volk, H-P Eberle, U Ortlepp, J R Producer: 20180315 In: Medizinische Klinik, Intensivmedizin und Notfallmedizin vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	The vitamin D receptor genotype predisposes to the development of calcific aortic valve stenosis. [electronic resource] by Ortlepp, J R Hoffmann, R Ohme, F Lauscher, J Bleckmann, F Hanrath, P Producer: 20010614 In: Heart (British Cardiac Society) vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The 4G/5G promotor polymorphism of the plasminogen activator inhibitor-1 gene and late lumen loss after coronary stent placement in smoking and nonsmoking patients. [electronic resource] by Ortlepp, J R Hoffmann, R Killian, A Lauscher, J Merkelbach-Brese, S Hanrath, P Producer: 20020111 In: Clinical cardiology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	The vitamin D receptor gene variant and physical activity predicts fasting glucose levels in healthy young men. [electronic resource] by Ortlepp, J R Metrikat, J Albrecht, M von Korff, A Hanrath, P Hoffmann, R Producer: 20031006 In: Diabetic medicine : a journal of the British Diabetic Association vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Quantitative trait loci for obesity and insulin resistance (Nob1, Nob2) and their interaction with the leptin receptor allele (LeprA720T/T1044I) in New Zealand obese mice. [electronic resource] by Kluge, R Giesen, K Bahrenberg, G Plum, L Ortlepp, J R Joost, H G Producer: 20010308 In: Diabetologia vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Type 2 diabetes-like hyperglycemia in a backcross model of NZO and SJL mice: characterization of a susceptibility locus on chromosome 4 and its relation with obesity. [electronic resource] by Plum, L Kluge, R Giesen, K Altmüller, J Ortlepp, J R Joost, H G Producer: 20000925 In: Diabetes vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Relation of body mass index, physical fitness, and the cardiovascular risk profile in 3127 young normal weight men with an apparently optimal lifestyle. [electronic resource] by Ortlepp, J R Metrikat, J Albrecht, M Maya-Pelzer, P Pongratz, H Hoffmann, R Producer: 20030825 In: International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A chymase gene variant is associated with atherosclerosis in venous coronary artery bypass grafts. [electronic resource] by Ortlepp, J R Janssens, U Bleckmann, F Lauscher, J Merkelbach-Bruse, S Hanrath, P Hoffmann, R Producer: 20011213 In: Coronary artery disease vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	A metabolic syndrome of hypertension, hyperinsulinaemia and hypercholesterolaemia in the New Zealand obese mouse. [electronic resource] by Ortlepp, J R Kluge, R Giesen, K Plum, L Radke, P Hanrath, P Joost, H G Producer: 20000413 In: European journal of clinical investigation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Robust association of the APOE epsilon4 allele with premature myocardial infarction especially in patients without hypercholesterolaemia: the Aachen study. [electronic resource] by Schmitz, F Mevissen, V Krantz, C Kimmel, M Erdmann, J Hoffmann, R Zerres, K Ortlepp, J R Producer: 20070629 In: European journal of clinical investigation vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Relation between the angiotensinogen (AGT) M235T gene polymorphism and blood pressure in a large, homogeneous study population. [electronic resource] by Ortlepp, J R Metrikat, J Mevissen, V Schmitz, F Albrecht, M Maya-Pelzer, P Hanrath, P Zerres, K Hoffmann, R Producer: 20031110 In: Journal of human hypertension vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Inhibition of the renin-angiotensin system ameliorates genetically determined hyperinsulinemia. [electronic resource] by Ortlepp, J R Breuer, J Eitner, F Kluge, K Kluge, R Floege, J Hollweg, G Hanrath, P Joost, H G Producer: 20020412 In: European journal of pharmacology vol. 436 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	APOE alleles are not associated with calcific aortic stenosis. [electronic resource] by Ortlepp, J R Pillich, M Mevissen, V Krantz, C Kimmel, M Autschbach, R Langebartels, G Erdmann, J Hoffmann, R Zerres, K Producer: 20061020 In: Heart (British Cardiac Society) vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene. [electronic resource] by Ortlepp, J R Vosberg, H P Reith, S Ohme, F Mahon, N G Schröder, D Klues, H G Hanrath, P McKenna, W J Producer: 20020226 In: Heart (British Cardiac Society) vol. 87 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 21 results.