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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

Parenteral nutrition in a premature infant with phenylketonuriaCOLE, D. E. C; LANDRY, D. A.JPEN. Journal of parenteral and enteral nutrition. 1984, Vol 8, Num 1, pp 42-44, issn 0148-6071Article

Newborn screening for phenylketonuria: predictive validity as a function of ageMCCABE, E. R. B; MCCABE, L; MOSHER, G. A et al.Pediatrics (Evanston). 1983, Vol 72, Num 3, pp 390-398, issn 0031-4005Article

Magnesium-deficient rickets in a phenylketonuric patient on dietary treatmentROTTOLI, A; RIVA, E; ZECCHINI, G et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 215-217, issn 0141-8955, suppl. 2Conference Paper

Dietary management of phenylketonuria from birth using a phenylalanine-free productFLANNERY, D. B; HITCHCOCK, E; MAMUNES, P et al.The Journal of pediatrics. 1983, Vol 103, Num 2, pp 247-249, issn 0022-3476Article

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

Purification and Use of Glycomacropeptide for Nutritional Manaqement of PhenylketonuriaLACLAIR, Caitlin E; NEY, Denise M; MACLEOD, Erin L et al.Journal of food science. 2009, Vol 74, Num 4, issn 0022-1147, E199-E206Article

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

Discrimination of phenylketonurics from persistent hyperphenylalaninemia patients using a simple phenylalanine loading testBLITZER, M. G; BAILEY-WILSON, J. E; SHAPIRA, E et al.Clinica chimica acta. 1985, Vol 153, Num 2, pp 137-142, issn 0009-8981Article

Clinical application of genotypic diagnosis for phenylketonuria : theoretical considerationsLEDLEY, F. D.European journal of pediatrics. 1991, Vol 150, Num 11, pp 752-756, issn 0340-6199Article

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

Immobilization of Phenylalanine Dehydrogenase and Its Application in Flow-Injection Analysis System for Determination of Plasma PhenylalanineTARHAN, Leman; AYAR-KAYALI, Hulya.Applied biochemistry and biotechnology. 2011, Vol 163, Num 2, pp 258-267, issn 0273-2289, 10 p.Article

Autism and phenylketonuriaBAIELI, Sabrina; PAVONE, Lorenzo; MELI, Concetta et al.Journal of autism and developmental disorders. 2003, Vol 33, Num 2, pp 201-204, issn 0162-3257, 4 p.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

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