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Early feeding practices in infants with phenylketonuria across Europe.
Mol Genet Metab Rep. 2018 Aug 8;16:82-89. doi: 10.1016/j.ymgmr.2018.07.008. eCollection 2018 Sep.
Mol Genet Metab Rep. 2018.
PMID: 30101073
Free PMC article.
Weaning practices in phenylketonuria vary between health professionals in Europe.
Pinto A, Adams S, Ahring K, Allen H, Almeida MF, Garcia-Arenas D, Arslan N, Assoun M, Atik Altınok Y, Barrio-Carreras D, Belanger Quintana A, Bernabei SM, Bontemps C, Boyle F, Bruni G, Bueno-Delgado M, Caine G, Carvalho R, Chrobot A, Chyż K, Cochrane B, Correia C, Corthouts K, Daly A, De Leo S, Desloovere A, De Meyer A, De Theux A, Didycz B, Dijsselhof ME, Dokoupil K, Drabik J, Dunlop C, Eberle-Pelloth W, Eftring K, Ekengren J, Errekalde I, Evans S, Foucart A, Fokkema L, François L, French M, Forssell E, Gingell C, Gonçalves C, Gökmen Özel H, Grimsley A, Gugelmo G, Gyüre E, Heller C, Hensler R, Jardim I, Joost C, Jörg-Streller M, Jouault C, Jung A, Kanthe M, Koç N, Kok IL, Kozanoğlu T, Kumru B, Lang F, Lang K, Liegeois I, Liguori A, Lilje R, Ļubina O, Manta-Vogli P, Mayr D, Meneses C, Newby C, Meyer U, Mexia S, Nicol C, Och U, Olivas SM, Pedrón-Giner C, Pereira R, Plutowska-Hoffmann K, Purves J, Re Dionigi A, Reinson K, Robert M, Robertson L, Rocha JC, Rohde C, Rosenbaum-Fabian S, Rossi A, Ruiz M, Saligova J, Gutiérrez-Sánchez A, Schlune A, Schulpis K, Serrano-Nieto J, Skarpalezou A, Skeath R, Slabbert A, Straczek K, Giżewska M, Terry A, Thom R, Tooke A, Tuokkola J, van Dam…
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Pinto A, et al. Among authors: chyz k.
Mol Genet Metab Rep. 2018 Nov 25;18:39-44. doi: 10.1016/j.ymgmr.2018.11.003. eCollection 2019 Mar.
Mol Genet Metab Rep. 2018.
PMID: 30705824
Free PMC article.
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Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria.
Bik-Multanowski M, Madetko-Talowska A, Betka I, Swieczka E, Didycz B, Orchel-Szastak K, Bik-Multanowska K, Starostecka E, Jaglowska J, Mozrzymas R, Zolkowska J, Chyz K, Korycinska-Chaaban D.
Bik-Multanowski M, et al. Among authors: chyz k.
Mol Genet Metab Rep. 2020 Aug 21;25:100640. doi: 10.1016/j.ymgmr.2020.100640. eCollection 2020 Dec.
Mol Genet Metab Rep. 2020.
PMID: 32874918
Free PMC article.
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Comparison of phenylalanine tolerance in singleton and twin pregnancies in patients with phenylketonuria.
Hozyasz KK, Żółkowska J, Chyż K.
Hozyasz KK, et al. Among authors: chyz k.
J Int Med Res. 2020 Sep;48(9):300060520934623. doi: 10.1177/0300060520934623.
J Int Med Res. 2020.
PMID: 32962492
Free PMC article.
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Undiagnosed Phenylketonuria Can Exist Everywhere: Results From an International Survey.
van Wegberg AMJ, Trefz F, Gizewska M, Ahmed S, Chabraoui L, Zaki MS, Maillot F, van Spronsen FJ; Study Group on Missed PKU and Missed to Follow-Up.
van Wegberg AMJ, et al.
J Pediatr. 2021 Dec;239:231-234.e2. doi: 10.1016/j.jpeds.2021.08.070. Epub 2021 Aug 30.
J Pediatr. 2021.
PMID: 34474089
Free article.
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