Zimmer, Klaus-Peter

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Journal Article

de Laffolie, Jan; Kamrath, Clemens; Burchert, Diana; Böttcher, Claudia; Wudy, Stefan Alexander; Zimmer, Klaus-Peter (2022). Reversible severe glycogenic hepatopathy in type 1 diabetes. Wiener medizinische Wochenschrift, 172(5-6), pp. 144-147. Springer 10.1007/s10354-020-00795-6

Waitz, Markus; Engel, Corinna; Schloesser, Rolf; Rochwalsky, Ulrich; Meyer, Sascha; Larsen, Alexander; Hoffmann, Paul; Zemlin, Michael; Bohnhorst, Bettina; Peter, Corinna; Hoppenz, Marc; Pabst, Thomas; Zimmer, Klaus-Peter; Franz, Axel R; Haertel, Christoph; Frieauff, Eric; Sandkötter, Julia; Masjosthusmann, Katja; Deindl, Philipp; Singer, Dominique; ... (2020). Application of two different nasal CPAP levels for the treatment of respiratory distress syndrome in preterm infants-"The OPTTIMMAL-Trial"-Optimizing PEEP To The IMMAture Lungs: study protocol of a randomized controlled trial. Trials, 21(1), p. 822. BioMed Central 10.1186/s13063-020-04660-0

Boettcher, Claudia; Sommer, Grit; Peitzsch, Mirko; Zimmer, Klaus-Peter; Eisenhofer, Graeme; Wudy, Stefan A (2020). Differential Responses of Urinary Epinephrine and Norepinephrine to 24-h Shift-Work Stressor in Physicians. Frontiers in endocrinology, 11, p. 572461. Frontiers Research Foundation 10.3389/fendo.2020.572461

Gilger, Mark; Hamaker, Bruce; Nichols, Buford L; Auricchio, Salvatore; Treem, William R; Naim, Hassan Y; Heine, Martin; Zimmer, Klaus-Peter; Jones, Kyra; Eskandari, Razieh; Pinto, B Mario; Rose, David R; Lee, Byung-Hoo; Quezada-Calvillo, Roberto; Adams, Bridget; Roach, Christine M; Ma, Chang-Xing; Baker, Susan S; Slawson, Mary H; Robayo-Torres, Claudia C; ... (2012). Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency Workshop. Journal of pediatric gastroenterology and nutrition, 55 Suppl 2(0 2), S1. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1097/00005176-199507000-00001

Alfalah, Marwan; Keiser, Markus; Leeb, Tosso; Zimmer, Klaus-Peter; Naim, Hassen Y. (2009). Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency. Gastroenterology, 136(3), pp. 883-892. Philadelphia, Pa.: Elsevier 10.1053/j.gastro.2008.11.038

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