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

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

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

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

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

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

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

HAEUFIGKEIT DER PHENYLKETONURIE-HETEROZYGOTIE = LA FREQUENCE DE LA PHENYLCETONURIE: HETEROZYGOTIETHEILE H.1980; KINDERAERZTL. PRAXIS; DDR; DA. 1980; VOL. 48; NO 8; PP. 434-435Article

MANAGEMENT OF PHENYLKETONURIA SOUTH AUSTRALIAN EXPERIENCE OF 13 CASES.ROBERTSON EF; HILL GN; CASHEL K et al.1976; MED. J. AUSTRAL.; AUSTRAL.; DA. 1976; VOL. 1; NO 18; PP. 647-650; BIBL. 13 REF.Article

SCREENING FOR ADULT PHENYLKETONURIA IN STATE PSYCHIATRIC HOSPITALSWILLETT AB; NELSON JE; FOSS DK et al.1980; AM. J. PSYCHIATRY; ISSN 0002-953X; USA; DA. 1980; VOL. 137; NO 12; PP. 1607-1608; BIBL. 9 REF.Article

BIOPTERIN DEFECT IN A NORMAL-APPEARING CHILD AFFECTED BY A TRANSIENT PHENYLKETONURIAREY F; LEEMING RJ; BLAIR JA et al.1980; ARCH. DIS. CHILD.; ISSN 0003-9888; GBR; DA. 1980; VOL. 55; NO 8; PP. 637-639; BIBL. 15 REF.Article

FETAL DAMAGE DESPITE LOW-PHENYLALANINE DIET AFTER CONCEPTION IN A PHENYLKETONURIC WOMANSMITH I; MACARTNEY FJ; ERDOHAZI M et al.1979; LANCET; GBR; DA. 1979; NO 8106; PP. 17-19; BIBL. 27 REF.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

ACCURACY OF NEWBORN SCREENING PROGRAMS FOR PHENYLKETONURIAKOCH R; FRIEDMAN EG.1981; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1981; VOL. 98; NO 2; PP. 267-269; BIBL. 10 REF.Article

REPRODUCTIVE COUNSELLING FOR ADOLESCENT FEMALES WITH PHENYLKETONURIATICE KS; WENZ E; JEW K et al.1980; J. INHERIT. METAB. DIS.; GBR; DA. 1980; VOL. 3; NO 3; PP. 105-107Article

GENETIC SCREENING OF THE NEWBORN IN AUSTRALIA: RESULTS FOR 1978PITT D; CONNELLY J; FRANCIS I et al.1979; MED. J. AUSTRAL.; AUS; DA. 1979; VOL. 2; NO 5; PP. 272-273; BIBL. 2 REF.Article

GENETICS OF THE MAMMALIAN PHENYLALANINE HYDROXYLASE SYSTEM: STUDIES OF HUMAN LIVER PHENYLALANINE HYDROXYLASE SUBUNIT STRUCTURE AND OF MUTATIONS IN PHENYLKETONURIACHOO KH; COTTON RGH; DANKS DM et al.1979; BIOCHEM. J.; GBR; DA. 1979; VOL. 181; NO 2; PP. 285-294; BIBL. 34 REF.Article

URINARY PHENYLETHYLAMINE EXCRETION. GAS CHROMATOGRAPHIC ASSAY WITH ELECTRON-CAPTURE DETECTION OF THE PENTAFLUOROBENZOYL DERIVATIVEBLAU K; CLAXTON IM; ISMAHAN G et al.1979; J. CHROMATOGR.; NLD; DA. 1979; VOL. 163; NO 2; PP. 135-142; BIBL. 19 REF.Article

A NEW VARIANT FORM OF PHENYLKETONURIAWATTS RWE; PURKISS P; CHALMERS RA et al.1979; QUART. J. MED.; GBR; DA. 1979; VOL. 48; NO 191; PP. 403-417; BIBL. 16 REF.Article

ATYPICAL PHENYLKETONURIA CAUSED BY 7,8-DIHYDROBIOPTERIN SYNTHETASE DEFICIENCYNIEDERWIESER A; CURTIUS HC; BETTONI O et al.1979; LANCET; GBR; DA. 1979; NO 8108; PP. 131-133; BIBL. 18 REF.Article

BEHAVIOURAL DEVIANCE IN CHILDREN WITH EARLY TREATED PHENYLKETONURIASTEVENSON JE; HAWCROFT J; LOBASCHER M et al.1979; ARCH. DIS. CHILDH.; GBR; DA. 1979; VOL. 54; NO 1; PP. 14-18; BIBL. 23 REF.Article