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Journal Abstract Search

167 related items for PubMed ID: 29651832

  • 21.
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  • 22. Phenylketonuria patients' and their parents' acceptance of the disease: multi-centre study.
    Witalis E, Mikoluc B, Motkowski R, Szyszko J, Chrobot A, Didycz B, Lange A, Mozrzymas R, Milanowski A, Nowacka M, Piotrowska-Depta M, Romanowska H, Starostecka E, Wierzba J, Skorniewska M, Wojcicka-Bartlomiejczyk BI, Gizewska M, Polish Society of Phenylketonuria.
    Qual Life Res; 2016 Nov; 25(11):2967-2975. PubMed ID: 27245777
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  • 23. Metabolomics for improved treatment monitoring of phenylketonuria: urinary biomarkers for non-invasive assessment of dietary adherence and nutritional deficiencies.
    Wild J, Shanmuganathan M, Hayashi M, Potter M, Britz-McKibbin P.
    Analyst; 2019 Nov 04; 144(22):6595-6608. PubMed ID: 31608347
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  • 24. Long-term follow-up and outcome of phenylketonuria patients on sapropterin: a retrospective study.
    Keil S, Anjema K, van Spronsen FJ, Lambruschini N, Burlina A, Bélanger-Quintana A, Couce ML, Feillet F, Cerone R, Lotz-Havla AS, Muntau AC, Bosch AM, Meli CA, Billette de Villemeur T, Kern I, Riva E, Giovannini M, Damaj L, Leuzzi V, Blau N.
    Pediatrics; 2013 Jun 04; 131(6):e1881-8. PubMed ID: 23690520
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  • 25. Non-PKU mild hyperphenylalaninemia (MHP)--the dilemma.
    Hanley WB.
    Mol Genet Metab; 2011 Jun 04; 104(1-2):23-6. PubMed ID: 21632269
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  • 27. Quality of life among parents of children with phenylketonuria (PKU).
    Fidika A, Salewski C, Goldbeck L.
    Health Qual Life Outcomes; 2013 Mar 28; 11():54. PubMed ID: 23537423
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  • 29. Unmet needs in phenylketonuria: an exploratory Italian survey among patients and caregivers.
    Rovelli V, Dicintio A, Cazzorla C.
    Curr Med Res Opin; 2024 May 02; ():1-11. PubMed ID: 38646665
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  • 31. Stability of blood phenylalanine levels and IQ in children with phenylketonuria.
    Anastasoaie V, Kurzius L, Forbes P, Waisbren S.
    Mol Genet Metab; 2008 May 02; 95(1-2):17-20. PubMed ID: 18703366
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  • 32. 5-year retrospective analysis of patients with phenylketonuria (PKU) and hyperphenylalaninemia treated at two specialized clinics.
    Levy H, Lamppu D, Anastosoaie V, Baker JL, DiBona K, Hawthorne S, Lindenberger J, Kinch D, Seymour A, McIlduff M, Watling S, Vockley J.
    Mol Genet Metab; 2020 Mar 02; 129(3):177-185. PubMed ID: 31883647
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  • 40. Health Related Quality of Life assessment among early-treated Hungarian adult PKU patients using the PKU-QOL adult questionnaire.
    Barta AG, Sumánszki C, Turgonyi Z, Kiss E, Simon E, Serfőző C, Reismann P.
    Mol Genet Metab Rep; 2020 Jun 02; 23():100589. PubMed ID: 32346514
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