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

Finding the fertile woman with phenylketonuriaHANLEY, William B.European journal of obstetrics, gynecology, and reproductive biology. 2008, Vol 137, Num 2, pp 131-135, issn 0301-2115, 5 p.Article

Rapid single-base mismatch detection in genotyping for phenylketonuriaTAKARADA, Yutaka; KAGAWA, Shohei; OKANO, Yoshiyuki et al.Molecular biotechnology. 2003, Vol 24, Num 3, pp 233-242, issn 1073-6085, 10 p.Article

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

Phenylketonuria: Diffusion magnetic resonance imaging and proton magnetic resonance spectroscopySENER, R. Nuri.Journal of computer assisted tomography. 2003, Vol 27, Num 4, pp 541-543, issn 0363-8715, 3 p.Article

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

Preliminary support for the oral administration of valine, isoleucine and leucine for phenylketonuriaJORDAN, M. K; BRUNNER, R. L; HUNT, M. M et al.Developmental medicine and child neurology (Print). 1985, Vol 27, Num 1, pp 33-39, issn 0012-1622Article

Les troubles du comportement au cours de la phénylcétonurie. Essai d'interprétation biochimique à partir d'une observation personnelle et d'une revue de la littérature = Behavioral aspects of phenylketonuria. Attempt at a biochemical interpretation from a personal case and a review of the literatureDALERY, J; MAILLET, J; DEVILLARD, R et al.L' Encéphale (Paris). 1983, Vol 9, Num 3, pp 279-290, issn 0013-7006Article

PHENYLKETONURIA AND ITS VARIANTS.KAUFMAN S; MILSTIEN S.1977; ANN. CLIN. LAB. SCI.; U.S.A.; DA. 1977; VOL. 7; NO 2; PP. 178-185; BIBL. 31 REF.Article

CONGENITAL AND NEUROLOGICAL ABNORMALITIES IN INFANTS WITH PHENYLKETONURIA.JOHNSON CF; KOCH R; PETERSON RM et al.1978; AMER. J. MENTAL DEFIC.; U.S.A.; DA. 1978; VOL. 82; NO 4; PP. 375-379; BIBL. 13 REF.Article

PHENYLKETONURIA (PKU) AND THE SINGLE GENE: AN OLD STORY RETOLDMURPHEY RM.1983; BEHAVIOR GENETICS; ISSN 0001-8244; USA; DA. 1983; VOL. 13; NO 2; PP. 141-157; BIBL. 4 P.Article

Maternal PhenylketonuriaPediatrics (Evanston). 2008, Vol 122, Num 2, pp 445-449, issn 0031-4005, 5 p.Article

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

Investigation of oxidative stress parameters in treated phenylketonuric patientsSITTA, A; BARSCHAK, A. G; DEON, M et al.Metabolic brain disease. 2006, Vol 21, Num 4, pp 287-296, issn 0885-7490, 10 p.Article

PHENYLALANINE LEVELS IN PKU FOLLOWING MINOR SURGERYFIEDLER AE; MILLER MJ; BICKEL H et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 4; PP. 411-414; BIBL. 4 REF.Article

Evidence that DNA damage is associated to phenylalanine blood levels in leukocytes from phenylketonuric patientsSITTA, Angela; MANFREDINI, Vanusa; BIASI, Lidiana et al.Mutation research. Genetic toxicology and environmental mutagenesis (Print). 2009, Vol 679, Num 1-2, pp 13-16, issn 1383-5718, 4 p.Article

A different approach to breast-feeding of the infant with phenylketonuriaVAN RIJN, Margreet; BEKHOF, Jolita; DIJKSTRA, Tietie et al.European journal of pediatrics. 2003, Vol 162, Num 5, pp 323-326, issn 0340-6199, 4 p.Article

PRELIMINARY REPORT ON THE EFFECTS OF DIET DISCONTINUATION IN PKUKOCH R; AZEN CG; FRIEDMAN EG et al.1982; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1982; VOL. 100; NO 6; PP. 870-875; BIBL. 28 REF.Article

ON ESTIMATING THE ACTUAL RATE OF FOETAL LOSS IN FAMILIES WITH AN AUTOSOMAL RECESSIVE DISORDER AND WOOLF'S DATA ON PKU.TEN KATE LP.1978; ANN. HUM. GENET.; G.B.; DA. 1978; VOL. 41; NO 4; PP. 463-464; BIBL. 3 REF.Article

A POSSIBLE REACTION TO PSEUDOEPHREDINE IN A PATIENT WITH PHENYKETONURIA.SPIELBERG SP; SCHULMAN JD.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 90; NO 6; PP. 1026; BIBL. 6 REF.Article

Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemiaFEILLET, Francois; CHERY, Céline; NAMOUR, Fares et al.Early human development. 2008, Vol 84, Num 9, pp 561-567, issn 0378-3782, 7 p.Article

Polyol Additives Modulate the In Vitro Stability and Activity of Recombinant Human Phenylalanine HydroxylaseNASCIMENTO, Cátia; LEANDRO, João; ROQUE LINO, Paulo et al.Applied biochemistry and biotechnology. 2010, Vol 162, Num 1, pp 192-207, issn 0273-2289, 16 p.Article

Adult issues in phenylketonuriaHOEKS, M. P. A; DEN HEIJER, M; JANSSEN, M. C. H et al.Netherlands journal of medicine. 2009, Vol 67, Num 1, pp 2-7, issn 0300-2977, 6 p.Article

Maternal phenylketonuria: Experiences from the United KingdomLEE, Philip J; LILBURN, Maggie; BAUDIN, Jenny et al.Pediatrics (Evanston). 2003, Vol 112, Num 6, pp 1553-1556, issn 0031-4005, 4 p., 2Conference Paper