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.
155 related articles for article (PubMed ID: 35270292)
1. Patient with Phenylketonuria and Intellectual Disability-Problem Not Always Caused Exclusively by Insufficient Metabolic Control (Coexistence of PKU and Alazami Syndrome). Patalan M; Leśniak A; Bernatowicz K; Romanowska H; Krzywińska-Zdeb E; Walczak M; Giżewska M Int J Environ Res Public Health; 2022 Feb; 19(5):. PubMed ID: 35270292 [TBL] [Abstract][Full Text] [Related]
2. A Chinese family with phenylketonuria and maternal phenylketonuria detected by family screening. Hsiao KJ; Chen CH; Chiu PC; Huang SC; Wuu KD Eur J Pediatr; 1986 Oct; 145(5):409-12. PubMed ID: 3792388 [TBL] [Abstract][Full Text] [Related]
3. Undiagnosed maternal phenylketonuria: own clinical experience and literature review. Bouchlariotou S; Tsikouras P; Maroulis G J Matern Fetal Neonatal Med; 2009 Oct; 22(10):943-8. PubMed ID: 19557660 [TBL] [Abstract][Full Text] [Related]
4. HPLC for confirmatory diagnosis and biochemical monitoring of Cuban patients with hyperphenylalaninemias. Contreras J; Alonso E; Fuentes LE MEDICC Rev; 2015 Jan; 17(1):23-8. PubMed ID: 25725765 [TBL] [Abstract][Full Text] [Related]
5. Maternal phenylketonuria in Turkey: outcomes of 71 pregnancies and issues in management. Yıldız Y; Sivri HS Eur J Pediatr; 2019 Jul; 178(7):1005-1011. PubMed ID: 31053953 [TBL] [Abstract][Full Text] [Related]
6. Can untreated PKU patients escape from intellectual disability? A systematic review. van Vliet D; van Wegberg AMJ; Ahring K; Bik-Multanowski M; Blau N; Bulut FD; Casas K; Didycz B; Djordjevic M; Federico A; Feillet F; Gizewska M; Gramer G; Hertecant JL; Hollak CEM; Jørgensen JV; Karall D; Landau Y; Leuzzi V; Mathisen P; Moseley K; Mungan NÖ; Nardecchia F; Õunap K; Powell KK; Ramachandran R; Rutsch F; Setoodeh A; Stojiljkovic M; Trefz FK; Usurelu N; Wilson C; van Karnebeek CD; Hanley WB; van Spronsen FJ Orphanet J Rare Dis; 2018 Aug; 13(1):149. PubMed ID: 30157945 [TBL] [Abstract][Full Text] [Related]
7. Phenylketonuria. Blau N; van Spronsen FJ; Levy HL Lancet; 2010 Oct; 376(9750):1417-27. PubMed ID: 20971365 [TBL] [Abstract][Full Text] [Related]
8. Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder. Yıldız Y; Dursun A; Tokatlı A; Coşkun T; Sivri HS Turk J Pediatr; 2016; 58(1):94-96. PubMed ID: 27922243 [TBL] [Abstract][Full Text] [Related]
9. Intellectual, neurologic, and neuropsychologic outcome in untreated subjects with nonphenylketonuria hyperphenylalaninemia. German Collaborative Study on Phenylketonuria. Weglage J; Ullrich K; Pietsch M; Fünders B; Güttler F; Harms E Pediatr Res; 1997 Sep; 42(3):378-84. PubMed ID: 9284280 [TBL] [Abstract][Full Text] [Related]
15. Phenylketonuria is still a major cause of mental retardation in Tunisia despite the possibility of treatment. Khemir S; El Asmi M; Sanhaji H; Feki M; Jemaa R; Tebib N; Dhondt JL; Ben Dridi MF; Mebazaa A; Kaabachi N Clin Neurol Neurosurg; 2011 Nov; 113(9):727-30. PubMed ID: 21862209 [TBL] [Abstract][Full Text] [Related]
16. Classical phenylketonuria presenting as maternal PKU syndrome in the offspring of an intellectually normal woman. Alghamdi MA; O'Donnell-Luria A; Almontashiri NA; AlAali WY; Ali HH; Levy HL JIMD Rep; 2023 Sep; 64(5):312-316. PubMed ID: 37701331 [TBL] [Abstract][Full Text] [Related]