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42. Different phenotypes for phenylalanine hydroxylase deficiency. Güttler F; Hansen G Ann Clin Biochem; 1977 May; 14(3):124-34. PubMed ID: 869488 [TBL] [Abstract][Full Text] [Related]
43. Detection of heterozygotes for phenylketonuria by constant intravenous infusion of L-phenylalanine. Jagenburg R; Rödjer S Clin Chem; 1977 Sep; 23(9):1661-5. PubMed ID: 890910 [TBL] [Abstract][Full Text] [Related]
44. Detection of phenylketonuria carriers. Kelly S; Rose F Public Health Rep (1896); 1969 Feb; 84(2):144-8. PubMed ID: 4980161 [No Abstract] [Full Text] [Related]
45. The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria. KNOX WE; MESSINGER EC Am J Hum Genet; 1958 Mar; 10(1):53-60. PubMed ID: 13520699 [No Abstract] [Full Text] [Related]
46. Another population of phenylketonuria? Studies on atypical phenylketonurics. Culley PD Dev Med Child Neurol; 1969 Dec; 11(6):718-29. PubMed ID: 5366192 [No Abstract] [Full Text] [Related]
47. Effects of oral contraceptives and obesity on carrier tests for phenylketonuria. Brown ES; Waisman HA; Swanson MA; Colwell RE; Banks ME; Gerritsen T Clin Chim Acta; 1973 Mar; 44(2):183-92. PubMed ID: 4699626 [No Abstract] [Full Text] [Related]
48. A case of phenylketonuria in the Eta resulting from the mating of a homozygous father and a heterozygous mother. FUJIKI N; DREW AL; MIYAKE M; NEMOTO H; SUJAKU C; SHIMADA T Am J Hum Genet; 1961 Mar; 13(1 Pt 1):64-8. PubMed ID: 13702464 [No Abstract] [Full Text] [Related]
49. [Intravenous loading of L-phenylalanine: detection of heterozygotes in phenylketonuria]. Lambert J; Viailhet M; Monot C; Lepoire E; Baradel J; Nabet P; Martin J; Pierson M C R Seances Soc Biol Fil; 1973; 167(3):502-8. PubMed ID: 4785089 [No Abstract] [Full Text] [Related]
51. Problems in the biochemical detection of heterozygotes for phenylketonuria. Yakymyshyn LY; Reid DW; Campbell DJ Clin Biochem; 1972 Mar; 5(1):73-81. PubMed ID: 5022449 [No Abstract] [Full Text] [Related]
52. Atypical phenylketonuria in a family with a phenylketonuric mother. Yu JS; O'Halloran MT Pediatrics; 1970 Nov; 46(5):707-11. PubMed ID: 5481071 [No Abstract] [Full Text] [Related]
53. A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria. Hilton MA; Sharpe JN; Hicks LG; Andrews BF J Pediatr; 1986 Oct; 109(4):601-4. PubMed ID: 3761073 [TBL] [Abstract][Full Text] [Related]
54. [The validity of a screening test of heterozygotes for phenylketonuria]. Giovannini M; Riva E; Stival G; Cividini D; Daroda C Minerva Pediatr; 1979 Nov; 31(21):1515-20. PubMed ID: 522842 [No Abstract] [Full Text] [Related]
55. Impaired phenylalanine-tyrosine conversion in patients with iron-deficiency anemia studied by a L-(2H5)phenylalanine-loading test. Lehmann WD; Heinrich HC Am J Clin Nutr; 1986 Oct; 44(4):468-74. PubMed ID: 3766433 [TBL] [Abstract][Full Text] [Related]
57. The NIH-shift in the in vivo hydroxylation of ring-deuterated L-phenylalanine in man. Lehmann WD; Heinrich HC Arch Biochem Biophys; 1986 Oct; 250(1):180-5. PubMed ID: 3767371 [TBL] [Abstract][Full Text] [Related]
58. [A study of phenylketonuria heterozygotes screening in married population of Tianjin area]. Song L; Xu F; Meng Y; Wang X; Liu C; Gao W; Shan Z; Liu C; Ding Z Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):56-8. PubMed ID: 11172645 [TBL] [Abstract][Full Text] [Related]
59. Plasma amino acid pattern in phenylketonuric heterozygotes during pregnancy. Cabalska B; Nowaczewska I; Duczyńska N Biochem Med; 1982 Jun; 27(3):269-77. PubMed ID: 7115361 [No Abstract] [Full Text] [Related]
60. Permanent chemical phenylketonuria and a normal phenylalanine tolerance in two sisters with a normal mental development. Wadman SK; Ketting D; De Bree PK; Van der Heiden C; Grimberg MT; Kruijswijk H Clin Chim Acta; 1975 Dec; 65(2):197-204. PubMed ID: 1183053 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]