Impact of medical genetics concerning phenylketonuria : accomplishments, status and practical future possibilitiesGUTTLER, F.Clinical genetics. 1989, Vol 36, Num 5, pp 333-334, issn 0009-9163, 2 p.Conference Paper

Atypical phenylketonuria with mild mental retardation caused by tetrahydrobiopterin deficiency in a Chinese familyHSIAO, K. J; CHIU, P.-C; CHENG, W.-H et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 240-243, issn 0141-8955, suppl. 2Conference Paper

Incidence of phenylketonuria and hyperphenylalaninaemia in a sample of the Turkish newborn populationOZALP, I; COSKUN, T; CEYHAN, M et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 237-239, issn 0141-8955, suppl. 2Conference Paper

Screening for phenylketonuria in Yugoslavia (SR Croatia) 1979―1984MARDESIC, D; GJURIC, G; JANCIKOVIC, J et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 234-236, issn 0141-8955, suppl. 2Conference Paper

Platelet phenylalanine hydroxylating activity in phenylketonurics and normal controlsUEBELHACK, R; FRANKE, L; KUTTER, D et al.Biochemical medicine. 1985, Vol 34, Num 3, pp 376-379, issn 0006-2944Article

Serum lipid concentrations in subjects with phenylketonuria and their familiesDECLUE, T. J; DAVIS, J; SCHOCKEN, D. M et al.American journal of diseases of children (1960). 1991, Vol 145, Num 11, pp 1266-1268, issn 0002-922XArticle

Children with phenylketonuria : the interface of family and child functioningSHULMAN, S; FISCH, R. O; ZEMPEL, C. E et al.Journal of developmental and behavioral pediatrics. 1991, Vol 12, Num 5, pp 315-321, issn 0196-206XArticle

Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiencyHOWELLS, D. W; FORREST, S. M; DAHL, H.-H. M et al.American journal of human genetics. 1990, Vol 47, Num 2, pp 279-285, issn 0002-9297, 7 p.Article

Phenylalanine metabolites as indicators of dietary compliance in children with phenylketonuriaMICHALS, K; LOPUS, M; MATALON, R et al.Biochemical medicine and metabolic biology. 1988, Vol 39, Num 1, pp 18-23, issn 0885-4505Article

Aspartame-sweetened beverage: effect on plasma amino acid concentrations in normal adults and adults heterozygous for phenylketonuriaSTEGINK, L. D; WOLF-NOVAK, L. C; FILER, L. J. JR et al.The Journal of nutrition. 1987, Vol 117, Num 11, pp 1989-1995, issn 0022-3166Article

Children of fathers with phenylketonuria : an international surveyFISCH, R. O; MATALON, R; WEISBERG, S et al.The Journal of pediatrics. 1991, Vol 118, Num 5, pp 739-741, issn 0022-3476Article

Préparation psychologique pour l'éducation d'enfants traités pour une phénylkétonurieBELOPOL'SKAYA, N. L.Defektologiâ. 1988, Num 2, pp 69-75, issn 0130-3074Article

Where do the depleted plasma amino acids go in phenylketonuria?CHRISTENSEN, H. N.Biochemical journal (London. 1906). 1986, Vol 236, Num 3, pp 929-930, issn 0006-2936Article

Newborn screening for phenylketonuria in eleven districtsLIU SHEN-RU; ZUO QI-HUA.Chinese medical journal. 1986, Vol 99, Num 2, pp 113-118, issn 0366-6999Article

Phenylalanine and other amino acids in phenylketonuriaCLEMENS, P. C; BURMESTER, J. G; PRANKEL, B. H et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 6, pp 1045-1046, issn 0141-8955Article

Paternal phenylketonuriaLEVY, H. L; LOBBREGT, D; KOCH, R et al.The Journal of pediatrics. 1991, Vol 118, Num 5, pp 741-743, issn 0022-3476Article

Dépistage néonatal de la phénylcétonurie et de l'hypothyroïdie. Un système d'optimisation = Neonatal screening of phenylketonuria and hypothyroidism : an optimizing systemREVIRON, D; AUQUIER, P; GIUSIANO, B et al.Archives françaises de pédiatrie. 1990, Vol 47, Num 4, pp 255-256, issn 0003-9764Article

Brief report: screening children with autism for fragile-X syndrome and phenylketonuriaPUESCHEL, S. M; HERMAN, R; GRODEN, G et al.Journal of autism and developmental disorders. 1985, Vol 15, Num 3, pp 335-338, issn 0162-3257Article

Detection of phynylketonuria in the very early newborn blood specimenDOHERTY, L. B; ROHR, F. J; LEVY, H. L et al.Pediatrics (Evanston). 1991, Vol 87, Num 2, pp 240-244, issn 0031-4005Article

Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuriaBÖHLES; ULLRICH, K; BEHBEHANI, A. W et al.European journal of pediatrics. 1991, Vol 150, Num 6, pp 425-428, issn 0340-6199Article

Pre-conceptual diatery management for maternal phenylketonuriaFARQUHAR, D. L; SIMPSON, G. K; STEVEN, F et al.Acta paediatrica scandinavica. 1987, Vol 76, Num 2, pp 279-283, issn 0001-656XArticle

Optimising growth in phenylketonuria: Current state of the clinical evidence baseDOKOUPIL, Katharina; GOKMEN-OZEL, Hulya; LAMMARDO, Anna Maria et al.Clinical nutrition (Edinburgh). 2012, Vol 31, Num 1, pp 16-21, issn 0261-5614, 6 p.Article

Tyrosine supplementation in the treatment of maternal phenylketonuriaROHR, F. J; LOBBREGT, D; LEVY, H. L et al.The American journal of clinical nutrition. 1998, Vol 67, Num 3, pp 473-476, issn 0002-9165Article

Magnetic resonance imaging of the brain in phenylketonuriaCLEARY, M. A; WALTER, J. H; WRAITH, J. E et al.Lancet (British edition). 1994, Vol 344, Num 8915, pp 87-90, issn 0140-6736Article

A treatment program for adolescents with phenylketonuriaGLEASON, L. A; MICHALS, K; MATALON, R et al.Clinical pediatrics. 1992, Vol 31, Num 6, pp 331-335, issn 0009-9228Article