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

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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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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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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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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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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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Relationship Among Genotype, Biochemical Phenotype, and Cognitive Performance in Females With Phenylalanine Hydroxylase Deficiency: Report From the Maternal Phenylketonuria Collabo... von Guttler, Flemming, Azen, Colleen, Guldberg, Per, Romstad, Anne, Hanley, William B, Levy, Harvey L, Matalon, Reuben, Rouse, Bobbye M, Trefz, Friedrich, de la Cruz, Felix, Koch, Richard

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

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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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The International Collaborative Study of Maternal Phenylketonuria: status report 1998 von Koch, R, Friedman, E, Azen, C, Hanley, W, Levy, H, Matalon, R, Rouse, B, Trefz, F, Waisbren, S, Michals-Matalon, K, Acosta, P, Güttler, F, Ullrich, K, Platt, L, de la Cruz, F

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PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population von Romano, V., Guldberg, P., Güttler, F., Meli, C., Mollica, F., Pavone, L., Giovannini, M., Riva, E., Biasucci, G., Luotti, D., Palillo, L., Calí, F., Ceratto, N., Anello, G., Bosco, P.

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

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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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‘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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Molecular Analysis of Phenylketonuria in Denmark: 99% of the Mutations Detected by Denaturing Gradient Gel Electrophoresis von Guldberg, Per, Henriksen, Karen Friis, Güttler, Flemming

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Mutation analysis of phenylketonuria in Yamagata prefecture, Japan von Kimura, Toshiyuki, Ikeda, Hiroyuki, Akaba, Kazuhiro, Guldberg, Per, Güttler, Flemming, Maki, Kazuko, Aikawa, Shogo, Hayasaka, Kiyoshi

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Phenotyping of phenylketonuric patients by oral phenylalanine loading von Ponzone, A, Spada, M, de Sanctis, L, Dianzani, I

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An occipito‐temporal syndrome in adolescents with optimally controlled hyperphenylalaninaemia von Lou, H. C., Toft, P. B., Andresen, J., Mikkelsen, I., Olsen, B., Güttler, F., Wieslander, S., Henriksen, O.

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