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European Journal of Pediatrics|January 1, 1990
Study design and description of patientsP Lutz, H Schmidt, U Batzler
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|February 1, 1989
[Differential diagnosis of increased phenylalanine blood level in infancy. Results of the German collaborative study on phenylketonuria (PKU)/hyperphenylalaninemia (HPA)]H Schmidt, P Lutz, U Batzler
European Journal of Pediatrics|January 1, 1990
Six-year follow up of phenylalanine intakes and plasma phenylalanine concentrationsU Wendel, K Ullrich, H Schmidt, et al.
European Journal of Pediatrics|January 1, 1990
Significance of the in vivo deuterated phenylalanine load for long-term phenylalanine tolerance and psycho-intellectual outcome in patients with PKUF K Trefz, U Batzler, T König, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1994
Growth and skeletal maturation in children with phenylketonuriaF Schaefer, P Burgard, U Batzler, et al.
European Journal of Pediatrics|January 1, 1990
Results of psychological testing of patients aged 3-6 yearsU Michel, E Schmidt, U Batzler
Journal of Inherited Metabolic Disease|January 1, 1982
Standardized loading test with protein for the differentiation of phenylketonuria from hyperphenylalaninaemiaP Lutz, H Schmidt, G Frey, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1984
[Initiation of treatment following screening for phenylketonuria]M Mahle, H Schmidt, P Lutz, et al.
European Journal of Pediatrics|October 12, 1978
Maple syrup urine disease: treatment of the acutely ill newbornG Hammersen, L Wille, H Schmidt, et al.
European Journal of Pediatrics|January 1, 1990
Preliminary neuropsychological test resultsL M de Sonneville, E Schmidt, U Michel, et al.
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