Continuous vs thrice-daily ceftazidime for elective intravenous antipseudomonal therapy in cystic fibrosis
Riethmueller, J, Junge, S, Schroeter, T. W, Kuemmerer, K, Franke, P, Ballmann, M, Claass, A, Broemme, S, Jeschke, R, Hebestreit, A, Staab, D, Koetz, K, Doering, G, Stern, M
Published in Infection (01.10.2009)
Published in Infection (01.10.2009)
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Tobramycin once- vs thrice-daily for elective intravenous antipseudomonal therapy in pediatric cystic fibrosis patients
Riethmueller, J, Ballmann, M, Schroeter, T. W, Franke, P, von Butler, R, Claass, A, Junge, S, Doering, G, Stern, M
Published in Infection (01.10.2009)
Published in Infection (01.10.2009)
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Technical note: Automatic evaluation of infrared thermal images by computerized active shape modeling of bovine udders challenged with Escherichia coli
Watz, S., Petzl, W., Zerbe, H., Rieger, A., Glas, A., Schröter, W., Landgraf, T., Metzner, M.
Published in Journal of dairy science (01.05.2019)
Published in Journal of dairy science (01.05.2019)
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Estimations on the degradability of ores and bacterial leaching activity using short‐time microcalorimetric tests
Schroeter, Achim W., Sand, W.
Published in FEMS Microbiology Reviews [FEMS MICROBIOL. REV.]. Vol. 11, no. 1-3. 1993 (01.07.1993)
Published in FEMS Microbiology Reviews [FEMS MICROBIOL. REV.]. Vol. 11, no. 1-3. 1993 (01.07.1993)
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Conference Proceeding
Electrical and Recombination Properties of Copper‐Silicide Precipitates in Silicon
Istratov, A. A., Hedemann, H., Seibt, M., Vyvenko, O. F., Schröter, W., Heiser, T., Flink, C., Hieslmair, H., Weber, E. R.
Published in Journal of the Electrochemical Society (01.11.1998)
Published in Journal of the Electrochemical Society (01.11.1998)
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Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis
Eber, Stefan W, Gonzalez, Jennifer M, Lux, Marcia L, Scarpa, Alphonse L, Tse, William T, Dornwell, Marion, Herbers, Jutta, Kugler, Wilfried, Ozcan, Refik, Pekrun, Arnulf, Gallagher, Patrick G, Schroter, Werner, Forget, Bernard G, Lux, Samuel E
Published in Nature genetics (01.06.1996)
Published in Nature genetics (01.06.1996)
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Eight novel mutations and consequences on mRNA and protein level in pyruvate kinase-deficient patients with nonspherocytic hemolytic anemia
Kugler, Wilfried, Willaschek, Christian, Holtz, Christiane, Ohlenbusch, Andreas, Laspe, Petra, Krügener, Regina, Muirhead, Hilary, Schröter, Werner, Lakomek, Max
Published in Human mutation (01.01.2000)
Published in Human mutation (01.01.2000)
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Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosis
Pekrun, A, Neubauer, B A, Eber, S W, Lakomek, M, Seidel, H, Schröter, W
Published in Clinical genetics (01.04.1995)
Published in Clinical genetics (01.04.1995)
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Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency
Eber, S W, Lande, W M, Iarocci, T A, Mentzer, W C, Höhn, P, Wiley, J S, Schröter, W
Published in British journal of haematology (01.07.1989)
Published in British journal of haematology (01.07.1989)
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Detection of Trace Amounts of Fetal RhD-Positive Red Cells with Flow Cytometry after Multiple Rh-Negative Intrauterine Transfusions and RhD-Gene Determination with PCR
Lynen, R., Legler, T.J., Maas, J.H., Suren, A., Osmers, R., Behring, B., Schroeter, W., Koehler, M.
Published in Transfusion medicine and hemotherapy (01.01.1996)
Published in Transfusion medicine and hemotherapy (01.01.1996)
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