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.
130 related articles for article (PubMed ID: 24607329)
1. Changes of lipoproteins in phenylalanine hydroxylase-deficient children during the first year of life. Nagasaka H; Tsukahara H; Okano Y; Hirano K; Sakurai T; Hui SP; Ohura T; Usui H; Yorifuji T; Hirayama S; Ohtake A; Miida T Clin Chim Acta; 2014 Jun; 433():1-4. PubMed ID: 24607329 [TBL] [Abstract][Full Text] [Related]
2. The association of serum lipids, lipoproteins and apolipoproteins with selected trace elements and minerals in phenylketonuric patients on diet. Schulpis KH; Karakonstantakis T; Bartzeliotou A; Karikas GA; Papassotiriou I Clin Nutr; 2004 Jun; 23(3):401-7. PubMed ID: 15158304 [TBL] [Abstract][Full Text] [Related]
3. Plasma cholesterol in adults with phenylketonuria. Williams RA; Hooper AJ; Bell DA; Mamotte CD; Burnett JR Pathology; 2015 Feb; 47(2):134-7. PubMed ID: 25551302 [TBL] [Abstract][Full Text] [Related]
4. Incidence of BH4-responsiveness in phenylalanine-hydroxylase-deficient Italian patients. Fiori L; Fiege B; Riva E; Giovannini M Mol Genet Metab; 2005 Dec; 86 Suppl 1():S67-74. PubMed ID: 16198137 [TBL] [Abstract][Full Text] [Related]
5. DNA methylated alleles of the phenylalanine hydroxylase promoter remodeled at elevated phenylalanine levels in newborns with hyperphenylalaninemia. Item CB; Farhadi S; Schanzer A; Greber-Platzer S Clin Biochem; 2017 Aug; 50(12):729-732. PubMed ID: 28389235 [TBL] [Abstract][Full Text] [Related]
6. Analysis of phenylalanine hydroxylase genotypes and hyperphenylalaninemia phenotypes using L-[1-13C]phenylalanine oxidation rates in vivo: a pilot study. Treacy EP; Delente JJ; Elkas G; Carter K; Lambert M; Waters PJ; Scriver CR Pediatr Res; 1997 Oct; 42(4):430-5. PubMed ID: 9380432 [TBL] [Abstract][Full Text] [Related]
9. Determination of phenylalanine hydroxylase activity in patients with phenylketonuria and hyperphenylalaninemia. Bartholomé K; Lutz P; Bickel H Pediatr Res; 1975 Dec; 9(12):899-903. PubMed ID: 1196708 [TBL] [Abstract][Full Text] [Related]
10. [Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]. Rey F; Abadie V; Lyonnet S; Berthelon M; Caillaud C; Melle D; Labrune P; Saudubray JM; Munnich A; Rey J Arch Fr Pediatr; 1992 Oct; 49(8):705-10. PubMed ID: 1288453 [TBL] [Abstract][Full Text] [Related]
11. In vivo studies of phenylalanine hydroxylase by phenylalanine breath test: diagnosis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency. Okano Y; Hase Y; Kawajiri M; Nishi Y; Inui K; Sakai N; Tanaka Y; Takatori K; Kajiwara M; Yamano T Pediatr Res; 2004 Nov; 56(5):714-9. PubMed ID: 15319459 [TBL] [Abstract][Full Text] [Related]
12. [Clinical study of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency in southern and northern Chinese patients]. Yang L; Zhang ZX; Ye J; Zhou ZS; Shen M; Han LS; Qiu W; Yu WM; Gu XF Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):310-3. PubMed ID: 17557244 [TBL] [Abstract][Full Text] [Related]
13. A defective splice site at the phenylalanine hydroxylase gene in phenylketonuria and benign hyperphenylalaninemia among Palestinian Arabs. Kleiman S; Bernstein J; Schwartz G; Eisensmith RC; Woo SL; Shiloh Y Hum Mutat; 1992; 1(4):340-3. PubMed ID: 1301942 [TBL] [Abstract][Full Text] [Related]
14. Long-term correction of hyperphenylalaninemia by AAV-mediated gene transfer leads to behavioral recovery in phenylketonuria mice. Mochizuki S; Mizukami H; Ogura T; Kure S; Ichinohe A; Kojima K; Matsubara Y; Kobayahi E; Okada T; Hoshika A; Ozawa K; Kume A Gene Ther; 2004 Jul; 11(13):1081-6. PubMed ID: 15057263 [TBL] [Abstract][Full Text] [Related]
15. Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemia. Feillet F; Chery C; Namour F; Kimmoun A; Favre E; Lorentz E; Battaglia-Hsu SF; Guéant JL Early Hum Dev; 2008 Sep; 84(9):561-7. PubMed ID: 18321666 [TBL] [Abstract][Full Text] [Related]
16. Validation of PAH genotype-based predictions of metabolic phenylalanine hydroxylase deficiency phenotype: investigation of PKU/MHP patients from Lithuania. Kasnauskiene J; Cimbalistiene L; Kucinskas V Med Sci Monit; 2003 Mar; 9(3):CR142-6. PubMed ID: 12640344 [TBL] [Abstract][Full Text] [Related]
17. Effect of repeated dietary counseling on serum lipoproteins from infancy to adulthood. Niinikoski H; Pahkala K; Ala-Korpela M; Viikari J; Rönnemaa T; Lagström H; Jokinen E; Jula A; Savolainen MJ; Simell O; Raitakari OT Pediatrics; 2012 Mar; 129(3):e704-13. PubMed ID: 22331346 [TBL] [Abstract][Full Text] [Related]
18. 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 [TBL] [Abstract][Full Text] [Related]
19. [Efficacy and safety of a phenylalanine-free amino acid-based enteral formula (AA-PKU2) in 1-8 year-old children with phenylketonuria: a prospective, open, self-controlled and multi-center study in China]. Zhou XL; Zhao ZY; Jiang JH; Zou H; Gu XF; Gu Q; Shen M; Lu J Zhongguo Dang Dai Er Ke Za Zhi; 2014 Jan; 16(1):11-5. PubMed ID: 24461170 [TBL] [Abstract][Full Text] [Related]
20. Optimal serum phenylalanine for adult patients with phenylketonuria. Okano Y; Nagasaka H Mol Genet Metab; 2013 Dec; 110(4):424-30. PubMed ID: 24094552 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]