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Published in The European physical journal. B, Condensed matter physics (01.06.2008)
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Published in European journal of radiology (01.11.2020)
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Hertz, J. M., Østergaard, K., Juncker, I., Pedersen, S., Romstad, A., Møller, L. B., Güttler, F., Dupont, E.
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Published in European radiology (01.09.2012)
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Published in American journal of human genetics (01.07.1998)
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Published in Pediatric research (01.05.2001)
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Published in American journal of human genetics (01.07.1996)
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Published in American journal of human genetics (01.07.1996)
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The International Study of Pregnancy Outcome in Women with Maternal Phenylketonuria: Report of a 12-year study
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Published in American journal of obstetrics and gynecology (01.02.2000)
Published in American journal of obstetrics and gynecology (01.02.2000)
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Güttler, F, Azen, C, Guldberg, P, Romstad, A, Hanley, W B, Levy, H L, Matalon, R, Rouse, B M, Trefz, F, de la Cruz, F, Koch, R
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Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria
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Published in The New England journal of medicine (02.05.1991)
Published in The New England journal of medicine (02.05.1991)
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Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)
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Published in Human genetics (01.12.2000)
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Phenylketonuria in adulthood: A collaborative study
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Published in Journal of inherited metabolic disease (01.09.2002)
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The International Collaborative Study of Maternal Phenylketonuria: status report 1998
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
Published in European journal of pediatrics (01.10.2000)
Published in European journal of pediatrics (01.10.2000)
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Double blind placebo control trial of large neutral amino acids in treatment of PKU: Effect on blood phenylalanine
Matalon, R., Michals‐Matalon, K., Bhatia, G., Burlina, A. B., Burlina, A. P., Braga, C., Fiori, L., Giovannini, M., Grechanina, E., Novikov, P., Grady, J., Tyring, S. K., Guttler, F.
Published in Journal of inherited metabolic disease (01.04.2007)
Published in Journal of inherited metabolic disease (01.04.2007)
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Large neutral amino acids in the treatment of phenylketonuria (PKU)
Matalon, R., Michals‐Matalon, K., Bhatia, G., Grechanina, E., Novikov, P., McDonald, J. D., Grady, J., Tyring, S. K., Guttler, F.
Published in Journal of inherited metabolic disease (01.12.2006)
Published in Journal of inherited metabolic disease (01.12.2006)
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A Phenylalanine Hydroxylase Amino Acid Polymorphism with Implications for Molecular Diagnostics
Gjetting, Torben, Romstad, Anne, Haavik, Jan, Knappskog, Per M., Acosta, Angelina X., Silva, W.Araújo, Zago, Marco A., Guldberg, Per, Gttler, Flemming
Published in Molecular genetics and metabolism (01.07.2001)
Published in Molecular genetics and metabolism (01.07.2001)
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PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population
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
Published in Journal of inherited metabolic disease (1996)
Published in Journal of inherited metabolic disease (1996)
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