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F K Trefz

Showing results (31-40 of 70) with videos related to

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The Journal of Pediatrics|December 1, 1995
Effect of high-dose tyrosine supplementation on brain function in adults with phenylketonuriaJ Pietz, R Landwehr, A Kutscha, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 1, 2000
Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: monitoring of treatment by carnitine/acylcarnitine analysis in blood spotsU Spiekerkötter, B Schwahn, H Korall, et al.
The Annals of Thoracic Surgery|October 18, 2001
Ventricular septal defect closure in a neonate with combined methylmalonic aciduria/homocystinuriaM K Heinemann, M Tomaske, F K Trefz, et al.
Biochemistry|September 8, 1992
Structural characterization of the 5' regions of the human phenylalanine hydroxylase geneD S Konecki, Y Wang, F K Trefz, et al.
European Journal of Pediatrics|December 1, 1993
Facilitation of hyperphenylalaninaemia phenotype assessment by genotype analysisD S Konecki, S Schweitzer-Krantz, D Byrd, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Relation between phenylalanine hydroxylase genotypes and phenotypic parameters of diagnosis and treatment of hyperphenylalaninaemic disorders. German Collaborative Study of PKUU Lichter-Konecki, A Rupp, D S Konecki, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Geographical distribution of the P281L mutation at the phenylalanine hydroxylase locus: possible origin in southeastern EuropeI Barić, D Mardesić, V Sarnavøka, et al.
European Journal of Pediatrics|April 1, 1993
3-Methylglutaconic aciduria in a patient with Pearson syndromeU Lichter-Konecki, F K Trefz, A Rötig, 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.
European Journal of Pediatrics|July 1, 1996
Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuriaP Burgard, A Rupp, D S Konecki, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
The Journal of Pediatrics|December 1, 1995
Effect of high-dose tyrosine supplementation on brain function in adults with phenylketonuriaJ Pietz, R Landwehr, A Kutscha, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 1, 2000
Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: monitoring of treatment by carnitine/acylcarnitine analysis in blood spotsU Spiekerkötter, B Schwahn, H Korall, et al.
The Annals of Thoracic Surgery|October 18, 2001
Ventricular septal defect closure in a neonate with combined methylmalonic aciduria/homocystinuriaM K Heinemann, M Tomaske, F K Trefz, et al.
Biochemistry|September 8, 1992
Structural characterization of the 5' regions of the human phenylalanine hydroxylase geneD S Konecki, Y Wang, F K Trefz, et al.
European Journal of Pediatrics|December 1, 1993
Facilitation of hyperphenylalaninaemia phenotype assessment by genotype analysisD S Konecki, S Schweitzer-Krantz, D Byrd, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Relation between phenylalanine hydroxylase genotypes and phenotypic parameters of diagnosis and treatment of hyperphenylalaninaemic disorders. German Collaborative Study of PKUU Lichter-Konecki, A Rupp, D S Konecki, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Geographical distribution of the P281L mutation at the phenylalanine hydroxylase locus: possible origin in southeastern EuropeI Barić, D Mardesić, V Sarnavøka, et al.
European Journal of Pediatrics|April 1, 1993
3-Methylglutaconic aciduria in a patient with Pearson syndromeU Lichter-Konecki, F K Trefz, A Rötig, 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.
European Journal of Pediatrics|July 1, 1996
Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuriaP Burgard, A Rupp, D S Konecki, et al.
Pageof 7