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Arteriosclerosis, Thrombosis, and Vascular Biology|September 4, 2004
Enzymatic modification of low-density lipoprotein in the arterial wall: a new role for plasmin and matrix metalloproteinases in atherogenesisMichael Torzewski, Prapat Suriyaphol, Kerstin Paprotka, et al.Thrombosis and Haemostasis|April 22, 2016
Antiphospholipid antibodies in a large population-based cohort: genome-wide associations and effects on monocyte gene expressionNadine Müller-Calleja, Heidi Rossmann, Christian Müller, et al.The British Journal of Ophthalmology|December 18, 2019
Prevalence of myopic maculopathy in the German population: results from the Gutenberg health studySusanne Hopf, Christina Korb, Stefan Nickels, et al.The Laryngoscope|December 14, 2021
Hearing Loss and Its Burden of Disease in a Large German Cohort-Hearing Loss in GermanyBerit Hackenberg, Julia Döge, Karl J Lackner, et al.Journal of Cardiovascular Medicine (Hagerstown, Md.)|December 23, 2021
Rationale and design of the effects of EMpagliflozin on left ventricular DIAstolic function in diabetes (EmDia) studyClaus Jünger, Jürgen H Prochaska, Tommaso Gori, et al.Clinical Chemistry and Laboratory Medicine|August 11, 2022
A novel point-of-care device accurately measures thyrotropin in whole blood, capillary blood and serumGeorge J Kahaly, Johannes Lotz, Sara Walder, et al.Biomolecules|July 25, 2018
Adverse Outcome Prediction of Iron Deficiency in Patients with Acute Coronary SyndromeTanja Zeller, Christoph Waldeyer, Francisco Ojeda, et al.Clinical Chemistry and Laboratory Medicine|February 11, 2018
Multicenter validation study for the certification of a CFTR gene scanning method using next generation sequencing technologyAnne Bergougnoux, Valeria D'Argenio, Stefanie Sollfrank, et al.Clinical Research in Cardiology : Official Journal of the German Cardiac Society|April 20, 2020
Midregional pro atrial natriuretic peptide: a novel important biomarker for noise annoyance-induced cardiovascular morbidity and mortality?Omar Hahad, Philipp S Wild, Jürgen H Prochaska, et al.Cancers|April 12, 2022
Second MAFA Variant Causing a Phosphorylation Defect in the Transactivation Domain and Familial InsulinomatosisChristian Fottner, Stefanie Sollfrank, Mursal Ghiasi, et al.Pageof 51