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High phenylalanine levels directly affect mood and sustained attention in adults with phenylketonuria: a randomised, double-blind, placebo-controlled, crossover trial.
J Inherit Metab Dis. 2011 Feb;34(1):165-71. doi: 10.1007/s10545-010-9253-9. Epub 2010 Dec 10.
J Inherit Metab Dis. 2011.
PMID: 21153445
Free PMC article.
Clinical Trial.
Parenting a child with phenylketonuria or galactosemia: implications for health-related quality of life.
ten Hoedt AE, Maurice-Stam H, Boelen CC, Rubio-Gozalbo ME, van Spronsen FJ, Wijburg FA, Bosch AM, Grootenhuis MA.
ten Hoedt AE, et al.
J Inherit Metab Dis. 2011 Apr;34(2):391-8. doi: 10.1007/s10545-010-9267-3. Epub 2011 Feb 3.
J Inherit Metab Dis. 2011.
PMID: 21290186
Free PMC article.
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"MY PKU": increasing self-management in patients with phenylketonuria. A randomized controlled trial.
Ten Hoedt AE, Hollak CE, Boelen CC, van der Herberg-van de Wetering NA, Ter Horst NM, Jonkers CF, Wijburg FA, Bosch AM.
Ten Hoedt AE, et al.
Orphanet J Rare Dis. 2011 Jun 27;6:48. doi: 10.1186/1750-1172-6-48.
Orphanet J Rare Dis. 2011.
PMID: 21708003
Free PMC article.
Clinical Trial.
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High incidence of hypermethioninaemia in a single neonatal intensive care unit detected by a newly introduced neonatal screening programme.
ten Hoedt AE, van Kempen AA, Boelen A, Duran M, Kemper-Proper EA, Oey-Spauwen MJ, Wijburg FA, Bosch AM.
ten Hoedt AE, et al.
J Inherit Metab Dis. 2007 Nov;30(6):978. doi: 10.1007/s10545-007-0701-0. Epub 2007 Sep 16.
J Inherit Metab Dis. 2007.
PMID: 17876719
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Monitoring phenylalanine concentrations in the follow-up of phenylketonuria patients: An inventory of pre-analytical and analytical variation.
Coene KLM, Timmer C, Goorden SMI, Ten Hoedt AE, Kluijtmans LAJ, Janssen MCH, Rennings AJM, Prinsen HCMT, Wamelink MMC, Ruijter GJG, Körver-Keularts IMLW, Heiner-Fokkema MR, van Spronsen FJ, Hollak CE, Vaz FM, Bosch AM, Huigen MCDG.
Coene KLM, et al. Among authors: ten hoedt ae.
JIMD Rep. 2020 Nov 22;58(1):70-79. doi: 10.1002/jmd2.12186. eCollection 2021 Mar.
JIMD Rep. 2020.
PMID: 33728249
Free PMC article.
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Psychosocial aspects of PKU: hidden disabilities--a review.
Gentile JK, Ten Hoedt AE, Bosch AM.
Gentile JK, et al. Among authors: ten hoedt ae.
Mol Genet Metab. 2010;99 Suppl 1:S64-7. doi: 10.1016/j.ymgme.2009.10.183.
Mol Genet Metab. 2010.
PMID: 20123473
Review.
Item in Clipboard
Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy.
Cullup T, Kho AL, Dionisi-Vici C, Brandmeier B, Smith F, Urry Z, Simpson MA, Yau S, Bertini E, McClelland V, Al-Owain M, Koelker S, Koerner C, Hoffmann GF, Wijburg FA, ten Hoedt AE, Rogers RC, Manchester D, Miyata R, Hayashi M, Said E, Soler D, Kroisel PM, Windpassinger C, Filloux FM, Al-Kaabi S, Hertecant J, Del Campo M, Buk S, Bodi I, Goebel HH, Sewry CA, Abbs S, Mohammed S, Josifova D, Gautel M, Jungbluth H.
Cullup T, et al. Among authors: ten hoedt ae.
Nat Genet. 2013 Jan;45(1):83-7. doi: 10.1038/ng.2497. Epub 2012 Dec 9.
Nat Genet. 2013.
PMID: 23222957
Free PMC article.
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An atypical course of coxsackievirus A6 associated hand, foot and mouth disease in extremely low birth weight preterm twins.
Bruning AH, van der Sanden SM, ten Hoedt AE, Wolthers KC, van Kaam AH, Pajkrt D.
Bruning AH, et al. Among authors: ten hoedt ae.
J Clin Virol. 2015 Apr;65:20-2. doi: 10.1016/j.jcv.2015.01.020. Epub 2015 Jan 29.
J Clin Virol. 2015.
PMID: 25766981
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