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European Journal of Clinical Pharmacology|January 1, 1988
Pharmacokinetics and pharmacodynamics of single oral doses of ibopamine, quinidine and their combination in normal manC de Mey, D Enterling, E Brendel, et al.
Macromolecular Rapid Communications|August 3, 2023
Correlating Molar Mass, π-Conjugation, and Optical Properties of Narrowly Distributed Anionic Polythiophenes in Aqueous SolutionsMartina Schmidt, Matthias Karg, Mukundan Thelakkat, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|August 15, 2015
Pattern phase diagram for two-dimensional arrays of coupled limit-cycle oscillatorsRoland Lauter, Christian Brendel, Steven J M Habraken, et al.
Kidney International|January 1, 1979
Biosynthesis of basement membrane matrix by isolated rat renal glomeruliJ T Hjelle, E C Carlson, K Brendel, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 12, 2019
Impact of Microphone Configuration on Speech Perception of Cochlear Implant Users in Traffic NoiseTobias Weissgerber, Mariana Bandeira, Martina Brendel, et al.
International Journal of Tissue Reactions|January 1, 1987
The dorsal skin-fold preparation of awake Syrian golden hamsters for assessment of microvascular permeability and microhaemodynamics with leukotriene C4P F Conzen, A E Goetz, F Deininger, et al.
Journal of Chromatography|October 16, 1987
Resolution of transducin subunits by chromatography on blue sepharoseC Kleuss, M Pallast, S Brendel, et al.
British Medical Journal|February 16, 1980
Emission and transmission brain tomographyP J Ell, J M Deacon, D Ducassou, et al.
Science Translational Medicine|August 24, 2022
Response to Comment on "Microglial activation states drive glucose uptake and FDG-PET alterations in neurodegenerative diseases"Xianyuan Xiang, Sabina Tahirovic, Sibylle Ziegler, et al.
American Journal of Medical Genetics. Part A|August 9, 2005
Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2Peter Huppke, Andreas Ohlenbusch, Cornelia Brendel, et al.
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