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Journal Abstract Search

159 related items for PubMed ID: 35855041

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  • 5. Undiagnosed phenylketonuria in parents of phenylketonuric patients, is it worthwhile to be checked?
    Wiedemann A, Leheup B, Battaglia-Hsu SF, Jonveaux P, Jeannesson E, Feillet F.
    Mol Genet Metab; 2013; 110 Suppl():S62-5. PubMed ID: 24051226
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  • 9. Development and psychometric validation of measures to assess the impact of phenylketonuria and its dietary treatment on patients' and parents' quality of life: the phenylketonuria - quality of life (PKU-QOL) questionnaires.
    Regnault A, Burlina A, Cunningham A, Bettiol E, Moreau-Stucker F, Benmedjahed K, Bosch AM.
    Orphanet J Rare Dis; 2015 May 10; 10():59. PubMed ID: 25958326
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  • 10. Child and parent attributions in chronic pediatric conditions: phenylketonuria (PKU) as an exemplar.
    Antshel KM, Brewster S, Waisbren SE.
    J Child Psychol Psychiatry; 2004 Mar 10; 45(3):622-30. PubMed ID: 15055380
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  • 12. Evaluation of patients diagnosed with phenylketonuria and biotinidase deficiency by the newborn screening program: a ten-year retrospective study.
    Toktaş İ, Sarıbaş S, Canpolat S, Erdem Ö, Özbek MN.
    Turk J Pediatr; 2022 Mar 10; 64(6):985-992. PubMed ID: 36583880
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  • 13. Phenylketonuria (PKU): screening and management.
    NIH Consens Statement; 2022 Mar 10; 17(3):1-33. PubMed ID: 11757784
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  • 16. Neonatal screening and long-term follow-up of phenylketonuria: the French database.
    Abadie V, Berthelot J, Feillet F, Maurin N, Mercier A, de Baulny HO, de Parscau L.
    Early Hum Dev; 2001 Dec 10; 65(2):149-58. PubMed ID: 11641035
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  • 20. Health status and comorbidities of adult patients with late-diagnosed phenylketonuria (PKU) born before the newborn screening in France - A nationwide study of health insurance claims data.
    Douillard C, Arnoux JB, Bouée S, Jacob C, Schneider KM, Theil J, Charrière S, Maillot F.
    Mol Genet Metab; 2023 Nov 10; 140(3):107704. PubMed ID: 37812967
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