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43. Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria. Hennermann JB; Loui A; Weber A; Mönch E J Perinat Med; 2004; 32(4):383-5. PubMed ID: 15346830 [TBL] [Abstract][Full Text] [Related]
44. VALIDATION OF A MODIFICATION OF THE GUTHRIE TEST FOR PHENYLKETONURIA. HAAB W; APPLETON MD; DUCH D; MURRAY R Am J Ment Defic; 1965 May; 69():790-3. PubMed ID: 14287813 [No Abstract] [Full Text] [Related]
45. [Congenital errors of metabolism: phenylketonuria and hyperphenylalanemias]. Laguna Serrano C An R Acad Nac Med (Madr); 1982; 99(4):783-814. PubMed ID: 7185286 [No Abstract] [Full Text] [Related]
46. [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]
47. [Early diagnosis of phenylketonuria (PKU). One year's experience with Guthrie's microbiological method]. Philipson A; Seim S; Werner B Lakartidningen; 1966 Jan; 63(3):199-206. PubMed ID: 5915190 [No Abstract] [Full Text] [Related]
49. [Screening for phenylketonuria without false readings from antibacterial agents]. Clemens P; Plettner C; Grüttner R Offentl Gesundheitswes; 1982 Jun; 44(6):435. PubMed ID: 6213907 [No Abstract] [Full Text] [Related]
50. 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]
54. 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]
55. Phenylketonuria. Nordmo SH S D J Med; 1966 Jan; 19(1):13-7. PubMed ID: 5215664 [No Abstract] [Full Text] [Related]
56. [Early systematic detection of phenylketonuria in the Lyon area using the Guthrie test]. Jeune M; Robert JM; Cotte J; Collombel C; Lamit J; Trouyez G Lyon Med; 1967 Jul; 218(27):7-17. PubMed ID: 5619179 [No Abstract] [Full Text] [Related]
58. 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]
59. The successful "Guthrie test" celebrates its 10th birthday in Brazil! Lopes ME Cien Saude Colet; 2011; 16 Suppl 1():716-7. PubMed ID: 21528612 [No Abstract] [Full Text] [Related]
60. Adverse medical outcomes of early newborn screening programs for phenylketonuria. Brosco JP; Sanders LM; Seider MI; Dunn AC Pediatrics; 2008 Jul; 122(1):192-7. PubMed ID: 18596006 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]