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Journal of Inherited Metabolic Disease|January 1, 1992
A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuriaU Langenbeck, A Behbehani, A Mench-HoinowskiJournal of Chromatography|September 1, 1978
Quantitative analysis of beta-phenylpyruvic acid by single ion monitoring. Evaluation of isomeric internal standardsU Langenbeck, A Mench-Hoinowski, I Rød-UrbanEuropean Journal of Pediatrics|August 1, 1980
Absence of a significant renal threshold for two aromatic acids in phenylketonuric children over two years of ageU Langenbeck, A Behbehani, A Mench-Hoinowski, et al.Journal of Mental Deficiency Research|September 1, 1986
Hyper-2-oxoglutaric aciduria in long-term mental handicapG Hoffmann, A Mench-Hoinowski, H Knüppel, et al.Journal of Inherited Metabolic Disease|January 26, 2006
Predicting the phenylalanine blood concentration from urine analyses. An approach to noninvasive monitoring of patients with phenylketonuriaU Langenbeck, F Baum, A Mench-Hoinowski, et al.Journal of Chromatography|March 1, 1978
O-trimethylsilylquinoxalinol derivatives of aromatic alpha-keto acids. Mass spectra and quantitative gas chromatographyU Langenbeck, A Mench-Hoinowski, K P Dieckmann, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine diseaseU Langenbeck, U Wendel, A Mench-Hoinowski, et al.Pageof 1