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2. [Thin layer chromatography separation and semi-quantitative determination of blood phenylalanine as procedure for the systematic screening of phenylketonuria in newborn infants]. Nitschké E Z Klin Chem Klin Biochem; 1968 May; 6(3):208-10. PubMed ID: 5709563 [No Abstract] [Full Text] [Related]
3. Neonatal screening for phenylketonuria. Netzloff ML Ann Clin Lab Sci; 1982; 12(5):368-71. PubMed ID: 7137934 [No Abstract] [Full Text] [Related]
4. Screening for phenylketonuria. Guthrie R Triangle; 1969; 9(3):104-9. PubMed ID: 5374132 [No Abstract] [Full Text] [Related]
6. Prospective study of early neonatal screening for phenylketonuria. Meryash DL; Levy HL; Guthrie R; Warner R; Bloom S; Carr JR N Engl J Med; 1981 Jan; 304(5):294-6. PubMed ID: 7442762 [No Abstract] [Full Text] [Related]
7. The Guthrie screening test for phenylketonuria: a report on two years participation in the national programme. Becroft DM; Horn CR N Z Med J; 1969 Apr; 69(443):212-5. PubMed ID: 5254295 [No Abstract] [Full Text] [Related]
8. 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]
9. Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia. Cunningham GC; Day RW; Berman JL; Hsia DY Am J Dis Child; 1969 Jun; 117(6):626-35. PubMed ID: 5771502 [No Abstract] [Full Text] [Related]
10. Phenylketonuria detected by the neonatal screening program in Thailand. Pangkanon S; Ratrisawadi V; Charoensiriwatana W; Techasena W; Boonpuan K; Srisomsap C; Svasti J Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():179-81. PubMed ID: 15906730 [TBL] [Abstract][Full Text] [Related]
15. Screening program for early detection of phenylketonuria in the newborn in Israel. Cohen BE; Szeinberg A; Peled I; Szeinberg B; Bar-Or R Isr J Med Sci; 1966; 2(2):156-64. PubMed ID: 5912550 [No Abstract] [Full Text] [Related]
16. [Use of an automated fluorometric method for detecting phenylketonuria]. Collombel C; Dorche C; Baltassat P; Cotte J Ann Biol Clin (Paris); 1969; 27(10):671-80. PubMed ID: 5374296 [No Abstract] [Full Text] [Related]
17. [Did the change of technique of screening investigations influence on improvement of test credibility in recognizing and differentiating diagnostics of hiperphenylalaninemias?]. Didycz B; Lemańska D; Słuszniak A Przegl Lek; 2009; 66(1-2):11-3. PubMed ID: 19485249 [TBL] [Abstract][Full Text] [Related]
18. Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria. Ponzone A; Spada M; Roasio L; Porta F; Mussa A; Ferraris S J Pediatr Gastroenterol Nutr; 2008 May; 46(5):561-9. PubMed ID: 18493213 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. [The clinical and molecular genetic characteristics of phenylketonuria patients in the Republic of Crimea]. Afanas'eva NA; Bychkova AM; Livshits LA; Bariliak IR Tsitol Genet; 1998; 32(1):8-14. PubMed ID: 9695246 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]