A Baseline for Multiple-Choice Testing in the University Classroom von Slepkov, A. D., Van Bussel, M. L., Fitze, K. M., Burr, W. S.

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Prenatal diagnosis of exomphalos and prediction of outcome von Nitzsche, K., Fitze, G., Rüdiger, M., Wimberger, P., Birdir, C.

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Commissioning experience and beam physics measurements at the SwissFEL Injector Test Facility von Schietinger, T., Pedrozzi, M., Aiba, M., Arsov, V., Bettoni, S., Beutner, B., Calvi, M., Craievich, P., Dehler, M., Frei, F., Ganter, R., Hauri, C. P., Ischebeck, R., Ivanisenko, Y., Janousch, M., Kaiser, M., Keil, B., Löhl, F., Orlandi, G. L., Ozkan Loch, C., Peier, P., Prat, E., Raguin, J.-Y., Reiche, S., Schilcher, T., Wiegand, P., Zimoch, E., Anicic, D., Armstrong, D., Baldinger, M., Baldinger, R., Bertrand, A., Bitterli, K., Bopp, M., Brands, H., Braun, H. H., Brönnimann, M., Brunnenkant, I., Chevtsov, P., Chrin, J., Citterio, A., Csatari Divall, M., Dach, M., Dax, A., Ditter, R., Divall, E., Falone, A., Fitze, H., Geiselhart, C., Guetg, M. W., Hämmerli, F., Hauff, A., Heiniger, M., Higgs, C., Hugentobler, W., Hunziker, S., Janser, G., Kalantari, B., Kalt, R., Kim, Y., Koprek, W., Korhonen, T., Krempaska, R., Laznovsky, M., Lehner, S., Le Pimpec, F., Lippuner, T., Lutz, H., Mair, S., Marcellini, F., Marinkovic, G., Menzel, R., Milas, N., Pal, T., Pollet, P., Portmann, W., Rezaeizadeh, A., Ritt, S., Rohrer, M., Schär, M., Schebacher, L., Scherrer, St, Schlott, V., Schmidt, T., Schulz, L., Smit, B., Stadler, M., Steffen, B., Stingelin, L., Sturzenegger, W., Treyer, D. M., Trisorio, A., Tron, W., Vicario, C., Zennaro, R., Zimoch, D.

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CONFLICT OVER MULTIPLE-PARTNER MATING BETWEEN MALES AND FEMALES OF THE POLYGYNANDROUS COMMON LIZARDS von Fitze, Patrick S, Le Galliard, Jean-François, Federici, Pierre, Richard, Murielle, Clobert, Jean

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Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR) von Fitze, Guido, Appelt, Hella, König, Inke R., Görgens, Heike, Stein, Ulrike, Walther, Wolfgang, Gossen, Manfred, Schreiber, Matthias, Ziegler, Andreas, Roesner, Dietmar, Schackert, Hans K.

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Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease von Fitze, Guido, Cramer, Jakob, Ziegler, Andreas, Schierz, Mandy, Schreiber, Matthias, Kuhlisch, Eberhard, Roesner, Dietmar, Schackert, Hans K

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Association of RET Protooncogene Codon 45 Polymorphism with Hirschsprung Disease von Fitze, Guido, Schreiber, Matthias, Kuhlisch, Eberhard, Schackert, Hans K., Roesner, Dietmar

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Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations von FITZE, Guido, SCHIERZ, Mandy, BREDOW, Jan, SAEGER, Hans D, ROESNER, Dietmar, SCHACKERT, Hans K

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Association of germline mutations and polymorphisms of the RET proto-oncogene with idiopathic congenital central hypoventilation syndrome in 33 patients von Fitze, G, Paditz, E, Schläfke, M, Kuhlisch, E, Roesner, D, Schackert, H K

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Cytosine deaminase 5-fluorocytosine gene therapy and Apo2L TRAIL cooperate to kill TRAIL-resistant tumor cells von Wei, J, Wahl, J, Knauss, H, Zeller, S, Jarmy, G, Fitze, G, Debatin, K-M, Beltinger, C

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Frequent loss of heterozygosity at the 19p13.3 locus without LKB1/STK11 mutations in human carcinoma metastases to the brain von SOBOTTKA, Stephan B, HAASE, Markus, FITZE, Guido, HAHN, Matthias, SCHACKERT, Hans K, SCHACKERT, Gabriele

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Within-Gene Interaction Between c.135 G/A Genotypes and RET Proto-Oncogene Germline Mutations in HSCR Families von Fitze, G., Cramer, J., Serra, A., Schreiber, M., Roesner, D., Schackert, H. K.

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Kogenitales zentrales Hypoventilationssyndrom mit Darmsymptomatik und Mutation des PHOX2B-Gens von Genz, K, Czernik, C, Fitze, G, Buttenberg, S, Obladen, M

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Interaction of RET proto-oncogene codon 609 germline mutations with RET haplotypes characterized by c.135G>A alleles modifying MEN 2A or HSCR phenotypes von Fitze, Guido, Schreiber, Matthias, Hohenberger, Werner, Hümmer, Hans Peter, Roesner, Dietmar, Schackert, Hans K.

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Mucoepidermoid carcinoma as an unusual cause for recurrent respiratory infections in a child von Vogelberg, Christian, Mohr, Brigitte, Fitze, Guido, Friedrich, Katrin, Hahn, Gabriele, Roesner, Dietmar, Leupold, Wolfgang, Suttorp, Meinolf

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Continuous thoracic epidural analgesia within a care pathway in young adolescents undergoing Nussʼ procedure for pectus excavatum repair: A-461 von Litz, R., Scheit, M., Gaebler, R., Fitze, G., Grosser, K., Koch, T., Heller, A. R.

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Evidence that TSG101 aberrant transcripts are PCR artifacts von Hampl, M, Hampl, J, Plaschke, J, Fitze, G, Schackert, G, Saeger, H D, Schackert, H K

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Multiple endocrine neoplasia type 2–associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors von Willeke, Frank, Hauer, Martin P., Buchcik, Rene, Gebert, Johannes F., Hahn, Matthias, Fitze, Guido, Mechtersheimer, Gunhild, Möller, Peter, Saeger, Hans-Detlev, Herfarth, Christian, Schackert, Hans K.

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Association between c135G/A phenotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease von Fitze, G, Cramer, J, Ziegler, A, Schierz, M, Schreiber, M, Kuhlisch, E, Roesner, D, Schackert, H K

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Kogenitales zentrales Hypoventilationssyndrom mit Darmsymptomatik und Mutation des PHOX2B-Gens von Genz, K, Czernik, C, Fitze, G, Buttenberg, S, Obladen, M

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