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22. Persistent tyrosinemia detected by thin-layer chromatography. Neto EC; Schulte J; Anele E; Becker D; Rubim R; Lewis E; De Mari J; Giugliani R Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():151. PubMed ID: 11400756 [TBL] [Abstract][Full Text] [Related]
23. A comparison of two laboratory techniques for early detection of phenylketonuria. Kugel RB; Lundgren RG; Fedge AK Am J Ment Defic; 1966 Sep; 71(2):244-8. PubMed ID: 5968857 [No Abstract] [Full Text] [Related]
24. Early blood sampling in neonatal programs for the detection of phenylketonuria. Szeinberg A; Cohen BE Padiatr Padol; 1982; 17(2):287-92. PubMed ID: 7099682 [TBL] [Abstract][Full Text] [Related]
26. A microplate-based enzymatic assay for the simultaneous determination of phenylalanine and tyrosine in serum. Wibrand F Clin Chim Acta; 2004 Sep; 347(1-2):89-96. PubMed ID: 15313145 [TBL] [Abstract][Full Text] [Related]
27. The search for phenylketonuria. Can Med Assoc J; 1969 Aug; 101(4):235-7. PubMed ID: 5817974 [No Abstract] [Full Text] [Related]
30. Screening for biopterin defects in newborns with phenylketonuria and other hyperphenylalaninemias. Matalon R; Michals K; Lee CL; Nixon JC Ann Clin Lab Sci; 1982; 12(5):411-4. PubMed ID: 6753726 [No Abstract] [Full Text] [Related]
31. [Our experiences with treatment of phenylketonuria]. Tresohlavá Z; Brachfeld K; Svatý J Cesk Pediatr; 1969 Jun; 24(6):522-8. PubMed ID: 5792287 [No Abstract] [Full Text] [Related]
32. [Phenylalanine level in the serum of heterozygotes for phenylketonuria under intensified protein catabolism]. Bliumina MG Genetika; 1981; 17(5):910-4. PubMed ID: 7195856 [TBL] [Abstract][Full Text] [Related]
33. [Malignant forms of phenylketonuria]. Bliumina MG Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(10):1462-5. PubMed ID: 6506948 [TBL] [Abstract][Full Text] [Related]
34. Determination of phenylalanine and tyrosine in dried blood specimens by ion-exchange chromatography using the Hitachi L-8800 analyzer. Allard P; Cowell LD; Zytkovicz TH; Korson MS; Ampola MG Clin Biochem; 2004 Oct; 37(10):857-62. PubMed ID: 15369715 [TBL] [Abstract][Full Text] [Related]
35. Cuban neonatal screening of phenylketonuria using an ultramicro-fluorometric test. González EC; Frómeta A; del Río L; Castells E; Robaina MS; García SM; Licourt T; Arteaga AL; Martínez L Clin Chim Acta; 2009 Apr; 402(1-2):129-32. PubMed ID: 19168043 [TBL] [Abstract][Full Text] [Related]
36. Neonatal screening for phenylketonuria. Netzloff ML Ann Clin Lab Sci; 1982; 12(5):368-71. PubMed ID: 7137934 [No Abstract] [Full Text] [Related]
37. [Detection of phenylketonuria using the urine and serum]. Simon K Med Monatsschr; 1968 Oct; 22(10):469-70. PubMed ID: 5712741 [No Abstract] [Full Text] [Related]
39. [Phenylketonuria and hyperphenylalaninemia: clinico-genetic classification of 14 forms]. Annenkov GA Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):351-6. PubMed ID: 6720175 [TBL] [Abstract][Full Text] [Related]