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F Trefz

Showing results (1-10 of 27) with videos related to

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Human Genetics|January 1, 1984
Compound heterozygotes in hyperphenylalaninaemiaK Bartholomé, K Olek, F Trefz
Molecular Genetics and Metabolism|September 28, 2011
Adult phenylketonuria outcome and managementF Trefz, F Maillot, K Motzfeldt, et al.
Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1972
[Proceedings: Isolation and quantitative determination of tryptophan metabolites with pyridine- and indole-structures in urine]D J Byrd, W Kochen, R Bühner, et al.
Studies in Health Technology and Informatics|October 18, 2001
RAMEDIS- rare metabolic diseases publishing tool for genotype-phenotype correlationU Mischke, U Scholz, T Toepel, et al.
Human Genetics|April 1, 1994
Neuropsychological and biochemical investigations in heterozygotes for phenylketonuria during ingestion of high dose aspartame (a sweetener containing phenylalanine)F Trefz, L de Sonneville, P Matthis, et al.
European Journal of Pediatrics|July 1, 1996
Outcome implications of the International Maternal Phenylketonuria Collaborative Study (MPKUCS): 1994R Koch, H Levy, W Hanley, et al.
The Journal of Pediatrics|January 15, 2000
Maternal phenylketonuria syndrome: congenital heart defects, microcephaly, and developmental outcomesB Rouse, R Matalon, R Koch, et al.
Clinical Nephrology|September 1, 1984
Idiopathic de Toni-Debré-Fanconi syndrome with absence of proximal tubular brush borderF Manz, R Waldherr, H P Fritz, et al.
American Journal of Medical Genetics|March 3, 1997
Maternal Phenylketonuria Collaborative Study (MPKUCS) offspring: facial anomalies, malformations, and early neurological sequelaeB Rouse, C Azen, R Koch, et al.
Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association|January 1, 1976
Indolic tryptophan metabolism in uraemiaD J Byrd, H W Berthold, K F Trefz, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Human Genetics|January 1, 1984
Compound heterozygotes in hyperphenylalaninaemiaK Bartholomé, K Olek, F Trefz
Molecular Genetics and Metabolism|September 28, 2011
Adult phenylketonuria outcome and managementF Trefz, F Maillot, K Motzfeldt, et al.
Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1972
[Proceedings: Isolation and quantitative determination of tryptophan metabolites with pyridine- and indole-structures in urine]D J Byrd, W Kochen, R Bühner, et al.
Studies in Health Technology and Informatics|October 18, 2001
RAMEDIS- rare metabolic diseases publishing tool for genotype-phenotype correlationU Mischke, U Scholz, T Toepel, et al.
Human Genetics|April 1, 1994
Neuropsychological and biochemical investigations in heterozygotes for phenylketonuria during ingestion of high dose aspartame (a sweetener containing phenylalanine)F Trefz, L de Sonneville, P Matthis, et al.
European Journal of Pediatrics|July 1, 1996
Outcome implications of the International Maternal Phenylketonuria Collaborative Study (MPKUCS): 1994R Koch, H Levy, W Hanley, et al.
The Journal of Pediatrics|January 15, 2000
Maternal phenylketonuria syndrome: congenital heart defects, microcephaly, and developmental outcomesB Rouse, R Matalon, R Koch, et al.
Clinical Nephrology|September 1, 1984
Idiopathic de Toni-Debré-Fanconi syndrome with absence of proximal tubular brush borderF Manz, R Waldherr, H P Fritz, et al.
American Journal of Medical Genetics|March 3, 1997
Maternal Phenylketonuria Collaborative Study (MPKUCS) offspring: facial anomalies, malformations, and early neurological sequelaeB Rouse, C Azen, R Koch, et al.
Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association|January 1, 1976
Indolic tryptophan metabolism in uraemiaD J Byrd, H W Berthold, K F Trefz, et al.
Pageof 3