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Items: 6

1.

Early feeding practices in infants with phenylketonuria across 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 E, van den Hurk TAM, van der Ploeg EMC, Vande Kerckhove K, Van Driessche M, van Wegberg AMJ, van Wyk K, Vasconcelos C, Velez García V, Wildgoose J, Winkler T, Żółkowska J, Zuvadelli J, MacDonald A.

Mol Genet Metab Rep. 2018 Aug 8;16:82-89. doi: 10.1016/j.ymgmr.2018.07.008. eCollection 2018 Sep.

2.

Body composition profile of young patients with phenylketonuria and mild hyperphenylalaninemia.

Doulgeraki A, Skarpalezou A, Theodosiadou A, Monopolis I, Schulpis K.

Int J Endocrinol Metab. 2014 Jul 1;12(3):e16061. doi: 10.5812/ijem.16061. eCollection 2014 Jul.

3.

Branched chain amino acids as adjunctive therapy to ketogenic diet in epilepsy: pilot study and hypothesis.

Evangeliou A, Spilioti M, Doulioglou V, Kalaidopoulou P, Ilias A, Skarpalezou A, Katsanika I, Kalamitsou S, Vasilaki K, Chatziioanidis I, Garganis K, Pavlou E, Varlamis S, Nikolaidis N.

J Child Neurol. 2009 Oct;24(10):1268-72. doi: 10.1177/0883073809336295. Epub 2009 Aug 17.

PMID:
19687389
4.

Application of a ketogenic diet in children with autistic behavior: pilot study.

Evangeliou A, Vlachonikolis I, Mihailidou H, Spilioti M, Skarpalezou A, Makaronas N, Prokopiou A, Christodoulou P, Liapi-Adamidou G, Helidonis E, Sbyrakis S, Smeitink J.

J Child Neurol. 2003 Feb;18(2):113-8.

PMID:
12693778
5.

Bone mineral status in children with phenylketonuria under treatment.

Al-Qadreh A, Schulpis KH, Athanasopoulou H, Mengreli C, Skarpalezou A, Voskaki I.

Acta Paediatr. 1998 Nov;87(11):1162-6.

PMID:
9846918
6.

Ornithine transcarbamylase deficiency: findings and treatment in a symptomatic female heterozygote.

Soulpis C, Markosoglou D, Papadelis F, Caraboula A, Giouroukos S, Skarpalezou A, Missìou-Tsagarakis S, Michelakakis H.

J Inherit Metab Dis. 1991;14(1):107-8. No abstract available.

PMID:
1861449

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