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Analytical and Quantitative Cytology and Histology|October 1, 1988
Macrophage size determinations in the diagnosis of tuberculous effusionsJ Guzman, U Costabel, K J Bross, et al.
Aktuelle Urologie|March 5, 2004
[Urodynamic findings in patients with infantile cerebral palsy]S Bross, S Pomer, L Döderlein, et al.
Skin Pharmacology and Physiology|July 19, 2014
Accelerated reepithelialization by triterpenes: proof of concept in the healing of surgical skin lesionsHans-Robert Metelmann, Johanna M Brandner, Hauke Schumann, et al.
Human Molecular Genetics|May 22, 2012
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiencyNanna Cornelius, Frank E Frerman, Thomas J Corydon, et al.
The Journal of Chemical Physics|January 22, 2021
Spectroscopic and theoretical studies of UN and UNS R Battey, D H Bross, K A Peterson, et al.
Human Mutation|August 29, 2001
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationshipN Gregersen, B S Andresen, M J Corydon, et al.
Molecular Genetics and Metabolism|February 4, 2014
Proteomic investigation of cultivated fibroblasts from patients with mitochondrial short-chain acyl-CoA dehydrogenase deficiencyAnders V Edhager, Vibeke Stenbroen, Nadia Sukusu Nielsen, et al.
Acta Cytologica|July 1, 1988
Malignant ascites of serous papillary ovarian adenocarcinoma. An immunocytochemical study of the tumor cellsJ Guzman, M Hilgarth, K J Bross, et al.
Biology Open|August 2, 2015
Structure and signaling at hydroid polyp-stolon junctions, revisitedKatherine L Harmata, Emily L Somova, Austin P Parrin, et al.
Blut|February 19, 1979
The use of lymphocyte phosphoglucomutase as a genetic marker in bone marrow transplant recipientsG M Schmidt, K G Blume, K J Bross, et al.
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