Phenylketonuria in adulthood: A collaborative study von Koch, R., Burton, B., Hoganson, G., Peterson, R., Rhead, W., Rouse, B., Scott, R., Wolff, J., Stern, A. M., Guttler, F., Nelson, M., la Cruz, F., Coldwell, J., Erbe, R., Geraghty, M. T., Shear, C., Thomas, J., Azen, C.

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Predictive information and explorative behavior of autonomous robots von Ay, N., Bertschinger, N., Der, R., Güttler, F., Olbrich, E.

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Mutation analysis anticipates dietary requirements in phenylketonuria von Güttler, F, Guldberg, P

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Forensic postmortem computed tomography in suspected unnatural adult deaths von Hueck, U., Muggenthaler, H., Hubig, M., Heinrich, A., Güttler, F., Wagner, R., Mall, G., Teichgräber, U.

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Privacy in VANETs using Changing Pseudonyms - Ideal and Real von Gerlach, M., Guttler, F.

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Maternal Phenylketonuria: An International Study von Koch, R., Hanley, W., Levy, H., Matalon, R., Rouse, B., Trefz, F., Guttler, F., Azen, C., Friedman, E., Platt, L., de la Cruz, F.

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A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype von Guldberg, Per, Rey, Françoise, Zschocke, Johannes, Romano, Valentino, François, Baudouin, Michiels, Luc, Ullrich, Kurt, Hoffmann, Georg F., Burgard, Peter, Schmidt, Hildgund, Meli, Concetta, Riva, Enrica, Dianzani, Irma, Ponzone, Alberto, Rey, Jean, Güttler, Flemming

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Benefits of Mutation Analysis and Examination of Brain Phenylalanine Levels in the Management of Phenylketonuria von Koch, Richard, Guttler, Flemming

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Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease von Hertz, J. M., Østergaard, K., Juncker, I., Pedersen, S., Romstad, A., Møller, L. B., Güttler, F., Dupont, E.

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‘Broad-range’ DGGE for single-step mutation scanning of entire genes: application to human phenylalanine hydroxylase gene von Guldberg, Per, Güttler, Flemming

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Fluorescence microscopy of single molecules von Güttler, Frank, Irngartinger, Thomas, Plakhotnik, Taras, Renn, Alois, Wild, Urs P.

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The Maternal Phenylketonuria International Study: 1984-2002 von KOCH, Richard, HANLEY, William, WAISBREN, Susan, WIDAMAN, Keith, JIAPING NING, FRIEDMAN, Eva G, DE LA CRUZ, Felix, LEVY, Harvey, MATALON, Kim, MATALON, Reuben, ROUSE, Bobbye, TREFZ, Frederick, GÜTTLER, Flemming, AZEN, Colleen, PLATT, Larry

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Tetrahydrobiopterin and maternal PKU von Koch, Richard, Moseley, Kathryn, Guttler, Flemming

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Magnetic resonance imaging of the active second stage of labour: Proof of principle von Güttler, F. V., Heinrich, A., Rump, J., de Bucourt, M., Schnackenburg, B., Bamberg, C., Hamm, B., Teichgräber, U. K.

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Danger of high‐protein dietary supplements to persons with hyperphenylalaninaemia von Koch, R., Moseley, K. D., Moats, R., Yano, S., Matalon, R., Guttler, F.

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Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland von Guldberg, P, Henriksen, K F, Sipilä, I, Güttler, F, de la Chapelle, A

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Single molecule spectroscopy: pressure effect on pentacene in p-terphenyl von Croci, Mauro, Müschenborn, Hans-Joachim, Güttler, Frank, Renn, Alois, Wild, Urs P.

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Modern techniques of differentiating the various phenotypes of phenylketonuria von Guttler, F

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Normal clinical outcome in untreated subjects with mild hyperphenylalaninemia von WEGLAGE, Josef, PIETSCH, Michael, MÖLLER, Harald, WENDEL, Udo, ULLRICH, Kurt, HARMS, Erik, FELDMANN, Reinhold, KOCH, Hans-Georg, ZSCHOCKE, Johannes, HOFFMANN, Georg, MUNTAU-HEGER, Anja, DENECKE, Jonas, GULDBERG, Per, GÜTTLER, Flemming

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Phenylalanine hydroxylase gene mutations in the United States : Report from the maternal PKU collaborative study von GULDBERG, P, LEVY, H. L, HANLEY, W. B, KOCH, R, MATALON, R, ROUSE, B. M, TREFZ, F, DE LA CRUZ, F, HENRIKSEN, K. F, GÜTTLER, F

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