'Broad-range' DGGE for single-step mutation scanning of entire genes: application to human phenylalanine hydroxylase gene.

Por Guldberg, P, Güttler, F
Publicado em 1994

A simple method for identification of point mutations using denaturing gradient gel electrophoresis.

Por Guldberg, P, Güttler, F
Publicado em 1993

Interaction of albumin and fusidic acid

Por Güttler, F., Tybring, L.
Publicado em 1971

Normal MPS excretion, but dermatan sulphaturia, combined with a mild Maroteaux-Lamy phenotype.

Por Tønnesen, T, Gregersen, H N, Güttler, F
Publicado em 1991

T lymphocyte function as the principal target of lymphocytic choriomeningitis virus-induced immunosuppression.

Por Bro-Jorgensen, K, Güttler, F, Jorgensen, P N, Volkert, M
Publicado em 1975

Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling.

Por Guldberg, P, Levy, H L, Henriksen, K F, Guttler, F
Publicado em 1996

Recurrent mutation in the human phenylalanine hydroxylase gene.

Por Okano, Y, Wang, T, Eisensmith, R C, Güttler, F, Woo, S L
Publicado em 1990

Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland.

Por Guldberg, P, Henriksen, K F, Sipilä, I, Güttler, F, de la Chapelle, A
Publicado em 1995

Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study.

Por 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.
Publicado em 1996

A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype.

Por Guldberg, P, Rey, F, Zschocke, J, Romano, V, François, B, Michiels, L, Ullrich, K, Hoffmann, G F, Burgard, P, Schmidt, H, Meli, C, Riva, E, Dianzani, I, Ponzone, A, Rey, J, Güttler, F
Publicado em 1998

Multiple origins for phenylketonuria in Europe

Por Eisensmith, R. C., Okano, Y., Dasovich, M., Wang, T., Güttler, F., Lou, H., Guldberg, P., Lichter-Konecki, U., Konecki, D. S., Svensson, E., Hagenfeldt, L., Rey, F., Munnich, A., Lyonnet, S., Cockburn, F., Connor, J. M., Pembrey, M. E., Smith, I., Gitzelmann, R., Steinmann, B., Apold, J., Eiken, H. G., Giovannini, M., Riva, E., Longhi, R., Romano, C., Cerone, R., Naughten, E. R., Mullins, C., Cahalane, S., Özalp, I., Fekete, G., Schuler, D., Berencsi, G. Y., Nász, I., Brdicka, R., Kamaryt, J., Pijackova, A., Cabalska, B., Boszkowa, K., Schwartz, E., Kalinin, V. N., Jin, L., Chakraborty, R., Woo, S. L. C.
Publicado em 1992