Results: 1-8 |
Results: 8

Authors: Gempel, K von Praun, C Baumkotter, J Lehnert, W Ensenauer, R Gerbitz, KD Bauer, MF
Citation: K. Gempel et al., "Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old child, EUR J PED, 160(9), 2001, pp. 548-551

Authors: Stadler, S Gempel, K Bieger, I Pontz, BF Gerbitz, KD Bauer, MF Hofmann, S
Citation: S. Stadler et al., Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry, J INH MET D, 24(3), 2001, pp. 370-378

Authors: Pfeiffer, A Bottcher, A Orso, E Kapinsky, M Nagy, P Bodnar, A Spreitzer, I Liebisch, G Drobnik, W Gempel, K Horn, M Holmer, S Hartung, T Multhoff, G Schutz, G Schindler, H Ulmer, AJ Heine, H Stelter, F Schutt, C Rothe, G Szollosi, J Damjanovich, S Schmitz, G
Citation: A. Pfeiffer et al., Lipopolysaccharide and ceramide docking to CD14 provokes ligand-specific receptor clustering in rafts, EUR J IMMUN, 31(11), 2001, pp. 3153-3164

Authors: Gempel, K Gerbitz, KD Casetta, B Bauer, MF
Citation: K. Gempel et al., Rapid determination of total homocysteine in blood spots by liquid chromatography-electrospray ionization-tandem mass spectrometry, CLIN CHEM, 46(1), 2000, pp. 122-123

Authors: Bauer, MF Gempel, K Hofmann, S Jaksch, M Philbrook, C Gerbitz, KD
Citation: Mf. Bauer et al., Mitochondrial disorders. A diagnostic challenge in clinical chemistry, CLIN CH L M, 37(9), 1999, pp. 855-876

Authors: Gempel, K Kottlors, M Jaksch, M Gerbitz, KD Bauer, MF
Citation: K. Gempel et al., Adult carnitine palmitoyltransferase II deficiency: Detection of characteristic carnitine esters in serum by tandem mass spectrometry, J INH MET D, 22(8), 1999, pp. 941-942

Authors: Bauer, MF Gempel, K Reichert, AS Rappold, GA Lichtner, P Gerbitz, KD Neupert, W Brunner, M Hofmann, S
Citation: Mf. Bauer et al., Genetic and structural characterization of the human mitochondrial inner membrane translocase, J MOL BIOL, 289(1), 1999, pp. 69-82

Authors: Burwinkel, B Kreuder, J Schweitzer, S Vorgerd, M Gempel, K Gerbitz, KD Kilimann, MW
Citation: B. Burwinkel et al., Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: A novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality, BIOC BIOP R, 261(2), 1999, pp. 484-487
Risultati: 1-8 |