Universitätsklinikum Hamburg-Eppendorf (UKE)

Improved agreement between experienced and inexperienced observers using a standardized evaluation protocol for cardiac volumetry and infarct size measurement (2012) Groth M, Muellerleile K, Klink T, Säring D, Halaj S, Folwarski G, Kaul M, et al. Journal article Cardiovascular computed tomography angiography in newborns and infants with suspected congenital heart disease: Retrospective evaluation of low-dose scan protocols (2012) Klink T, Müller G, Weil J, Dodge-Khatami A, Adam G, Bley TA Journal article Measurement of TLR-induced macrophage spreading by automated image analysis: Differential role of Myd88 and MAPK in early and late responses (2011) Wenzel J, Held C, Palmisano R, Teufel S, David JP, Wittenberg T, Lang R Journal article, Original article B-cell receptor epitope recognition correlates with the clinical course of chronic lymphocytic leukemia (2011) Binder M, Müller F, Jackst A, Léchenne B, Pantic M, Bacher U, Zu Eulenburg C, et al. Journal article Impact of the coxsackievirus and adenovirus receptor on the adenoma-carcinoma sequence of colon cancer (2011) Stecker K, Vieth M, Koschel A, Wiedenmann B, Röcken C, Anders M Journal article Diagnosis and therapy of cutaneous and mucocutaneous Leishmaniasis in Germany (2011) Boecken G, Sunderkötter C, Bogdan C, Weitzel T, Fischer M, Müller A, Löbermann M, et al. Journal article Bone marrow-derived progenitor cells do not contribute to podocyte turnover in the puromycin aminoglycoside and renal ablation models in rats (2011) Meyer-Schwesinger C, Lange C, Broecker V, Agustian PA, Lehmann U, Raabe A, Brinkmeyer M, et al. Journal article Hämolytisch-urämisches Syndrom durch EHEC O104:H4 – Ein erster Überblick über die Epidemie 2011 (2011) Kielstein JT, Schiffer M, Panzer U, Brunkhorst R Journal article NOD2/CARD15 gene polymorphisms affect outcome in pediatric allogeneic stem cell transplantation (2011) Kreyenberg H, Jarisch A, Bayer C, Schuster B, Willasch A, Strahm B, Kremens B, et al. Journal article Ccdc66 null mutation causes retinal degeneration and dysfunction (2011) Gerding WM, Schreiber S, Schulte-Middelmann T, Marques ADC, Atorf J, Akkad DA, Dekomien G, et al. Journal article