These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
1295 related items for PubMed ID: 14654659
1. Impact of the phenylalanine hydroxylase gene on maternal phenylketonuria outcome. Güttler F, Azen C, Guldberg P, Romstad A, Hanley WB, Levy HL, Matalon R, Rouse BM, Trefz F, de la Cruz F, Koch R. Pediatrics; 2003 Dec; 112(6 Pt 2):1530-3. PubMed ID: 14654659 [Abstract] [Full Text] [Related]
2. Pregnancy experiences in the woman with mild hyperphenylalaninemia. Levy HL, Waisbren SE, Güttler F, Hanley WB, Matalon R, Rouse B, Trefz FK, de la Cruz F, Azen CG, Koch R. Pediatrics; 2003 Dec; 112(6 Pt 2):1548-52. PubMed ID: 14654663 [Abstract] [Full Text] [Related]
3. Potential role of tetrahydrobiopterin in the treatment of maternal phenylketonuria. Trefz FK, Blau N. Pediatrics; 2003 Dec; 112(6 Pt 2):1566-9. PubMed ID: 14654666 [Abstract] [Full Text] [Related]
4. Relation of prenatal phenylalanine exposure to infant and childhood cognitive outcomes: results from the International Maternal PKU Collaborative Study. Widaman KF, Azen C. Pediatrics; 2003 Dec; 112(6 Pt 2):1537-43. PubMed ID: 14654661 [Abstract] [Full Text] [Related]
12. [Comparison of genotype and intellectual phenotype in untreated phenylketonuric children]. Yuan L, Fang B, Wang M, Wang T, Huang S, Yang T, Zhao S. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Oct 10; 15(5):297-9. PubMed ID: 9758878 [Abstract] [Full Text] [Related]
15. Molecular basis of phenylketonuria and a correlation between genotype and phenotype in a heterogeneous southeastern US population. Eisensmith RC, Martinez DR, Kuzmin AI, Goltsov AA, Brown A, Singh R, Elsas LJ II, Woo SL. Pediatrics; 1996 Apr 10; 97(4):512-6. PubMed ID: 8632937 [Abstract] [Full Text] [Related]
16. Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency. Ponzone A, Porta F, Mussa A, Alluto A, Ferraris S, Spada M. Metabolism; 2010 May 10; 59(5):645-52. PubMed ID: 19913839 [Abstract] [Full Text] [Related]
17. 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 May 10; 45(6):320-3. PubMed ID: 15868846 [Abstract] [Full Text] [Related]