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Items: 1 to 20 of 139

1.

Early dietary treated patients with phenylketonuria can achieve normal growth and body composition.

Rocha JC, van Spronsen FJ, Almeida MF, Ramos E, Guimarães JT, Borges N.

Mol Genet Metab. 2013;110 Suppl:S40-3. doi: 10.1016/j.ymgme.2013.10.009. Epub 2013 Oct 22.

PMID:
24183791
2.

Evaluation of nutritional status and pathophysiology of growth retardation in patients with phenylketonuria.

Dobbelaere D, Michaud L, Debrabander A, Vanderbecken S, Gottrand F, Turck D, Farriaux JP.

J Inherit Metab Dis. 2003;26(1):1-11.

PMID:
12872834
3.

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. Epub 2007 Jul 11. Review.

PMID:
17628756
4.

Nutrient intakes and physical growth of children with phenylketonuria undergoing nutrition therapy.

Acosta PB, Yannicelli S, Singh R, Mofidi S, Steiner R, DeVincentis E, Jurecki E, Bernstein L, Gleason S, Chetty M, Rouse B.

J Am Diet Assoc. 2003 Sep;103(9):1167-73.

PMID:
12963945
5.

Body protein in prepubertal children with phenylketonuria.

Allen JR, Baur LA, Waters DL, Humphries IR, Allen BJ, Roberts DC, Gaskin KJ.

Eur J Clin Nutr. 1996 Mar;50(3):178-86.

PMID:
8654332
6.

[Evaluation of physical development in children with classical phenylketonuria].

Bushueva TV, Borovik TE, Ladodo KS, Kuzenkova LM, Maslova OI, Gevorkyan AK.

Vopr Pitan. 2015;84(2):34-43. Russian.

PMID:
26841554
7.

Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: impact on growth in PKU.

Aldámiz-Echevarría L, Bueno MA, Couce ML, Lage S, Dalmau J, Vitoria I, Andrade F, Llarena M, Blasco J, Alcalde C, Gil D, García MC, González-Lamuño D, Ruiz M, Ruiz MA, González D, Sánchez-Valverde F.

Mol Genet Metab. 2013 Aug;109(4):331-8. doi: 10.1016/j.ymgme.2013.05.017. Epub 2013 Jun 4. Erratum in: Mol Genet Metab. 2015 Mar;114(3):485.

PMID:
23810227
8.

Carnitine status in early-treated children, adolescents and young adults with phenylketonuria on low phenylalanine diets.

Weigel C, Kiener C, Meier N, Schmid P, Rauh M, Rascher W, Knerr I.

Ann Nutr Metab. 2008;53(2):91-5. doi: 10.1159/000165356. Epub 2008 Oct 22.

PMID:
18946205
9.

Does impaired growth of PKU patients correlate with the strictness of dietary treatment? National Dutch PKU Steering Committee.

van Spronsen FJ, Verkerk PH, van Houten M, Smit GP, van der Meer SB, Bakker HD, Sengers RC.

Acta Paediatr. 1997 Aug;86(8):816-8.

PMID:
9307159
10.

Whole body composition analysis by the BodPod air-displacement plethysmography method in children with phenylketonuria shows a higher body fat percentage.

Albersen M, Bonthuis M, de Roos NM, van den Hurk DA, Carbasius Weber E, Hendriks MM, de Sain-van der Velden MG, de Koning TJ, Visser G.

J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S283-8. doi: 10.1007/s10545-010-9149-8. Epub 2010 Jun 24.

11.

Mental health and social functioning in early treated Phenylketonuria: the PKU-COBESO study.

Jahja R, Huijbregts SC, de Sonneville LM, van der Meere JJ, Bosch AM, Hollak CE, Rubio-Gozalbo ME, Brouwers MC, Hofstede FC, de Vries MC, Janssen MC, van der Ploeg AT, Langendonk JG, van Spronsen FJ.

Mol Genet Metab. 2013;110 Suppl:S57-61. doi: 10.1016/j.ymgme.2013.10.011. Epub 2013 Oct 22.

PMID:
24183792
12.

6R-tetrahydrobiopterin treated PKU patients below 4 years of age: Physical outcomes, nutrition and genotype.

Aldámiz-Echevarría L, Bueno MA, Couce ML, Lage S, Dalmau J, Vitoria I, Llarena M, Andrade F, Blasco J, Alcalde C, Gil D, García MC, González-Lamuño D, Ruiz M, Ruiz MA, Peña-Quintana L, González D, Sánchez-Valverde F.

Mol Genet Metab. 2015 May;115(1):10-6. doi: 10.1016/j.ymgme.2015.03.007. Epub 2015 Apr 1.

PMID:
25882749
13.

Relationships between lumbar bone mineral density and biochemical parameters in phenylketonuria patients.

de Groot MJ, Hoeksma M, van Rijn M, Slart RH, van Spronsen FJ.

Mol Genet Metab. 2012 Apr;105(4):566-70. doi: 10.1016/j.ymgme.2012.01.006. Epub 2012 Jan 16.

PMID:
22300845
14.

A new, low-volume protein substitute for teenagers and adults with phenylketonuria.

MacDonald A, Lilburn M, Cochrane B, Davies P, Daly A, Asplin D, Hall SK, Cousins A, Chakrapani A, Robinson P, Lee P.

J Inherit Metab Dis. 2004;27(2):127-35.

PMID:
15159643
15.

Physical development in patients with phenylketonuria on dietary treatment: a retrospective study.

Belanger-Quintana A, Martínez-Pardo M.

Mol Genet Metab. 2011 Dec;104(4):480-4. doi: 10.1016/j.ymgme.2011.08.002. Epub 2011 Aug 10.

PMID:
21878401
16.

Nutritional evaluation of children with phenylketonuria.

Fisberg RM, da Silva-Fernandes ME, Schmidt BJ, Fisberg M.

Sao Paulo Med J. 1999 Sep 2;117(5):185-91.

17.

Growth and skeletal maturation in children with phenylketonuria.

Schaefer F, Burgard P, Batzler U, Rupp A, Schmidt H, Gilli G, Bickel H, Bremer HJ.

Acta Paediatr. 1994 May;83(5):534-41.

PMID:
8086734
18.

Neurocognitive functioning in adults with phenylketonuria: results of a long term study.

Weglage J, Fromm J, van Teeffelen-Heithoff A, Möller HE, Koletzko B, Marquardt T, Rutsch F, Feldmann R.

Mol Genet Metab. 2013;110 Suppl:S44-8. doi: 10.1016/j.ymgme.2013.08.013. Epub 2013 Aug 31.

PMID:
24071437
19.

Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients.

Aldámiz-Echevarría L, Bueno MA, Couce ML, Lage S, Dalmau J, Vitoria I, Andrade F, Blasco J, Alcalde C, Gil D, García MC, González-Lamuño D, Ruiz M, Peña-Quintana L, Ruiz MA, González D, Sánchez-Valverde F.

Clin Nutr. 2014 Aug;33(4):702-17. doi: 10.1016/j.clnu.2013.09.011. Epub 2013 Sep 26.

PMID:
24120886
20.

Event-related potential correlates of selective processing in early- and continuously-treated children with phenylketonuria: effects of concurrent phenylalanine level and dietary control.

de Sonneville LM, Huijbregts SC, van Spronsen FJ, Verkerk PH, Sergeant JA, Licht R.

Mol Genet Metab. 2010;99 Suppl 1:S10-7. doi: 10.1016/j.ymgme.2009.10.177.

PMID:
20123462

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