Muendlein, Axel

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Xu, Yanning; Derakhshan, Arash; Hysaj, Ola; Wildisen, Lea; Ittermann, Till; Pingitore, Alessandro; Abolhassani, Nazanin; Medici, Marco; Kiemeney, Lambertus A L M; Riksen, Niels P; Dullaart, Robin P F; Trompet, Stella; Dörr, Marcus; Brown, Suzanne J; Schmidt, Börge; Führer-Sakel, Dagmar; Vanderpump, Mark P J; Muendlein, Axel; Drexel, Heinz; Fink, Howard A; ... (2023). The optimal healthy ranges of thyroid function defined by the risk of cardiovascular disease and mortality: systematic review and individual participant data meta-analysis. The lancet. Diabetes & endocrinology, 11(10), pp. 743-754. Elsevier 10.1016/S2213-8587(23)00227-9

Geiger, Kathrin; Zach, Christina; Leiherer, Andreas; Fraunberger, Peter; Drexel, Heinz; Muendlein, Axel (2020). Real-time PCR based HLA-B*27 screening directly in whole blood. HLA : immune response genetic, 95(3), pp. 189-195. Wiley 10.1111/tan.13767

Muendlein, Axel; Geiger, Kathrin; Leiherer, Andreas; Saely, Christoph H; Fraunberger, Peter; Drexel, Heinz (2020). Evaluation of the association between circulating microRNAs and kidney function in coronary angiography patients. American journal of physiology. Renal physiology, 318(2), F315-F321. American Physiological Society 10.1152/ajprenal.00429.2019

Leiherer, Andreas; Ebner, Janine; Muendlein, Axel; Brandtner, Eva M; Zach, Christina; Geiger, Kathrin; Fraunberger, Peter; Drexel, Heinz (2020). Data on the power of high betatrophin to predict cardiovascular deaths in coronary patients. Data in brief, 28(104989), p. 104989. 10.1016/j.dib.2019.104989

Leiherer, Andreas; Ebner, Janine; Muendlein, Axel; Brandtner, Eva M; Zach, Christina; Geiger, Kathrin; Fraunberger, Peter; Drexel, Heinz (2020). High betatrophin in coronary patients protects from cardiovascular events. Atherosclerosis, 293, pp. 62-68. Elsevier 10.1016/j.atherosclerosis.2019.11.011

Leiherer, Andreas; Muendlein, Axel; Christoph H, Saely; Reijo, Laaksonen; Mita, Lääperi; Alexander, Vonbank; Mader, Arthur; Fraunberger, Peter; Baumgartner, Iris; Dopheide, Jörn Fredrik; Drexel, Heinz (11 November 2019). Serum Ceramides and Type 2 Diabetes Are Mutually Independent Predictors of Cardiovascular Events in Patients With Peripheral Artery Disease. Circulation, Vol. 140(Suppl_1). American Heart Association, Inc

Leiherer, Andreas; Muendlein, Axel; Saely, Christoph H; Fraunberger, Peter; Drexel, Heinz (2019). Serotonin is elevated in risk-genotype carriers of TCF7L2 - rs7903146. Scientific reports, 9(1), p. 12863. Springer Nature 10.1038/s41598-019-49347-y

Drexel, Heinz; Leiherer, Andreas; Saely, Christoph H; Brandtner, Eva Maria; Geiger, Kathrin; Vonbank, Alexander; Fraunberger, Pater; Muendlein, Axel (2019). Are SGLT2 polymorphisms linked to diabetes mellitus and cardiovascular disease? Prospective study and meta-analysis. Bioscience reports, 39(8) Portland Press 10.1042/BSR20190299

Muendlein, Axel; Leiherer, Andreas; Saely, Christoph; Ebner, Janine; Geiger, Kathrin; Brandtner, Eva Maria; Vonbank, Alexander; Fraunberger, Peter; Drexel, Heinz (2019). Data on the association between CTRP1 and future major adverse cardiovascular events in patients undergoing coronary angiography. Data in brief, 25, p. 104109. Elsevier 10.1016/j.dib.2019.104109

Muendlein, Axel; Leiherer, Andreas; Saely, Christoph; Ebner, Janine; Geiger, Kathrin; Brandtner, Eva Maria; Vonbank, Alexander; Fraunberger, Peter; Drexel, Heinz (2019). The novel adipokine CTRP1 is significantly associated with the incidence of major adverse cardiovascular events. Atherosclerosis, 286, pp. 1-6. Elsevier 10.1016/j.atherosclerosis.2019.04.222

Muendlein, Axel; Leiherer, Andreas; Zach, Christina; Brandtner, Eva Maria; Fraunberger, Peter; Drexel, Heinz; Geiger, Kathrin (2019). Real-time PCR based detection of the lactase non-persistence associated genetic variant LCT-13910C>T directly from whole blood. Molecular biology reports, 46(2), pp. 2379-2385. Springer 10.1007/s11033-019-04696-9

Geiger, Kathrin; Leiherer, Andreas; Brandtner, Eva-Maria; Fraunberger, Peter; Drexel, Heinz; Muendlein, Axel (2019). Direct blood PCR: TaqMan-probe based detection of the venous thromboembolism associated mutations factor V Leiden and prothrombin c.20210G>A without DNA extraction. Clinica chimica acta, 488, pp. 221-225. Elsevier 10.1016/j.cca.2018.11.016

Zach, Christina; Unterkofler, Karl; Fraunberger, Peter; Drexel, Heinz; Muendlein, Axel (2019). Unrecognized High Occurrence of Genetically Confirmed Hereditary Carnitine Palmitoyltransferase II Deficiency in an Austrian Family Points to the Ongoing Underdiagnosis of the Disease. Frontiers in genetics, 10(497), p. 497. Frontiers Media SA 10.3389/fgene.2019.00497

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