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2. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria. Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181 [TBL] [Abstract][Full Text] [Related]
3. [Embryofetopathy of the newborn infant of a phenylketonuric mother. A diagnosis not to be missed]. Farriaux JP; Dhondt JL; Largillière C; Lacombe A; Valat S; Puech F J Gynecol Obstet Biol Reprod (Paris); 1993; 22(1):49-52. PubMed ID: 8463567 [TBL] [Abstract][Full Text] [Related]
4. Maternal phenylketonuria: a metabolic teratogen. Levy HL; Ghavami M Teratology; 1996 Mar; 53(3):176-84. PubMed ID: 8761885 [TBL] [Abstract][Full Text] [Related]
12. Lactation and phenylketonuria. Bradburn NC; Wappner RS; Lemons JA; Meyer BA; Roberts RS Am J Perinatol; 1985 Apr; 2(2):138-41. PubMed ID: 4096753 [TBL] [Abstract][Full Text] [Related]
13. [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]
14. Maternal phenylketonuria: an international study. Koch R; Hanley W; Levy H; Matalon R; Rouse B; Trefz F; Guttler F; Azen C; Friedman E; Platt L; de la Cruz F Mol Genet Metab; 2000; 71(1-2):233-9. PubMed ID: 11001815 [TBL] [Abstract][Full Text] [Related]
15. Phenylalanine hydroxylase deficiency: intelligence of patients after early dietary treatment. Chien YH; Chiang SC; Huang A; Lin JM; Chiu YN; Chou SP; Wang TR; Hwu WL Acta Paediatr Taiwan; 2004; 45(6):320-3. PubMed ID: 15868846 [TBL] [Abstract][Full Text] [Related]
16. Detection of phenylketonuria by the newborn screening program in Thailand. Pangkanon S; Charoensiriwatana W; Janejai N; Boonwanich W; Chaisomchit S Southeast Asian J Trop Med Public Health; 2009 May; 40(3):525-9. PubMed ID: 19842439 [TBL] [Abstract][Full Text] [Related]
17. [Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases]. Campistol Plana J; Arellano Pedrola M; Poo Argüelles P; Escofet Sotera C; Pérez Olarte P; Vilaseca Buscà MA An Esp Pediatr; 1999 Aug; 51(2):139-42. PubMed ID: 10495499 [TBL] [Abstract][Full Text] [Related]
18. Learning and behavioural difficulties but not microcephaly in three brothers resulting from undiagnosed maternal phenylketonuria. Shaw-Smith C; Hogg SL; Reading R; Calvin J; Trump D Child Care Health Dev; 2004 Sep; 30(5):551-5. PubMed ID: 15320931 [TBL] [Abstract][Full Text] [Related]
19. Phenylketonuria and maternal phenylketonuria. Purnell H Breastfeed Rev; 2001 Jul; 9(2):19-21. PubMed ID: 11550601 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]