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Items: 1 to 20 of 27

1.

Executive functioning in children and adolescents with phenylketonuria.

VanZutphen K, Packman W, Sporri L, Needham M, Morgan C, Weisiger K, Packman S.

Clin Genet. 2007 Jul;72(1):13-8.

PMID:
17594394
2.

Executive function in early-treated phenylketonuria: profile and underlying mechanisms.

Christ SE, Huijbregts SC, de Sonneville LM, White DA.

Mol Genet Metab. 2010;99 Suppl 1:S22-32. doi: 10.1016/j.ymgme.2009.10.007. Review.

PMID:
20123466
3.

Executive functioning in context: Relevance for treatment and monitoring of phenylketonuria.

Huijbregts SC, Gassió R, Campistol J.

Mol Genet Metab. 2013;110 Suppl:S25-30. doi: 10.1016/j.ymgme.2013.10.001. Review.

PMID:
24206933
4.

[Phenylketonuria: a children's disease in adulthood].

de Valk HW, de Sonneville LM, Duran M, Poll-The BT, Erkelens DW.

Ned Tijdschr Geneeskd. 2000 Jan 1;144(1):11-5. Review. Dutch.

PMID:
10665298
5.

The role of intelligence in phenylketonuria: a review of research and management.

Brumm VL, Grant ML.

Mol Genet Metab. 2010;99 Suppl 1:S18-21. doi: 10.1016/j.ymgme.2009.10.015. Review.

PMID:
20123465
6.

Phenylalanine levels of 6-10 mg/dl may not be as benign as once thought.

Diamond A.

Acta Paediatr Suppl. 1994 Dec;407:89-91. Review.

PMID:
7766969
7.

The reality of dietary compliance in the management of phenylketonuria.

MacDonald A, Gokmen-Ozel H, van Rijn M, Burgard P.

J Inherit Metab Dis. 2010 Dec;33(6):665-70. doi: 10.1007/s10545-010-9073-y. Review.

PMID:
20373144
8.

A prefrontal dysfunction model of early-treated phenylketonuria.

Welsh MC.

Eur J Pediatr. 1996 Jul;155 Suppl 1:S87-9. Review.

PMID:
8828618
9.

Review of neuropsychological functioning in treated phenylketonuria: an information processing approach.

Waisbren SE, Brown MJ, de Sonneville LM, Levy HL.

Acta Paediatr Suppl. 1994 Dec;407:98-103. Review.

PMID:
7766971
10.

Outcomes beyond phenylalanine: an international perspective.

Feillet F, MacDonald A, Hartung Perron D, Burton B.

Mol Genet Metab. 2010;99 Suppl 1:S79-85. doi: 10.1016/j.ymgme.2009.09.015. Review.

PMID:
20123476
11.

Behaviour in early treated phenylketonuria: a systematic review.

Smith I, Knowles J.

Eur J Pediatr. 2000 Oct;159 Suppl 2:S89-93. Review.

PMID:
11043152
12.

PKU in adolescents: rationale and psychosocial factors in diet continuation.

Levy HL, Waisbren SE.

Acta Paediatr Suppl. 1994 Dec;407:92-7. Review.

PMID:
7766970
13.

Maternal phenylketonuria: an international study.

Koch R, Hanley W, Levy H, Matalon R, Rouse B, Trefz F, Guttler F, Azen C, Friedman E, Platt L, de la Cruz F.

Mol Genet Metab. 2000 Sep-Oct;71(1-2):233-9. Review.

PMID:
11001815
14.

Omega-3 LC-PUFA supply and neurological outcomes in children with phenylketonuria (PKU).

Koletzko B, Beblo S, Demmelmair H, Hanebutt FL.

J Pediatr Gastroenterol Nutr. 2009 Mar;48 Suppl 1:S2-7. doi: 10.1097/MPG.0b013e3181977399. Review.

PMID:
19214054
15.

Growth and body composition in children with classical phenylketonuria: results in 34 patients and review of the literature.

Huemer M, Huemer C, Möslinger D, Huter D, Stöckler-Ipsiroglu S.

J Inherit Metab Dis. 2007 Oct;30(5):694-9. Review.

PMID:
17628756
16.

Adult phenylketonuria outcome and management.

Trefz F, Maillot F, Motzfeldt K, Schwarz M.

Mol Genet Metab. 2011;104 Suppl:S26-30. doi: 10.1016/j.ymgme.2011.08.025. Review.

PMID:
21944883
17.

Neuropsychological approaches to treatment policy issues in phenylketonuria.

Griffiths P.

Eur J Pediatr. 2000 Oct;159 Suppl 2:S82-6. Review.

PMID:
11043151
18.

Beyond executive function: non-executive cognitive abilities in individuals with PKU.

Janzen D, Nguyen M.

Mol Genet Metab. 2010;99 Suppl 1:S47-51. doi: 10.1016/j.ymgme.2009.10.009. Review.

PMID:
20123470
19.

Neuropsychological speed tests and blood phenylalanine levels in patients with phenylketonuria: a meta-analysis.

Albrecht J, Garbade SF, Burgard P.

Neurosci Biobehav Rev. 2009 Mar;33(3):414-21. doi: 10.1016/j.neubiorev.2008.11.001. Review.

PMID:
19038285
20.

The truth of treating patients with phenylketonuria after childhood: the need for a new guideline.

van Spronsen FJ, Burgard P.

J Inherit Metab Dis. 2008 Dec;31(6):673-9. doi: 10.1007/s10545-008-0918-6. Review.

PMID:
18690552

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