University of Groningen
PKU dietary handbook to accompany PKU guidelines (vol 15, 171, 2020)
MacDonald, A.; van Wegberg, A. M. J.; Ahring, K.; Beblo, S.; Belanger-Quintana, A.; Burlina,
A.; Campistol, J.; Coskun, T.; Feillet, F.; Gizewska, M.
Published in:
Orphanet journal of rare diseases
DOI:
10.1186/s13023-020-01486-6
IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from
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Document Version
Publisher's PDF, also known as Version of record
Publication date:
2020
Link to publication in University of Groningen/UMCG research database
Citation for published version (APA):
MacDonald, A., van Wegberg, A. M. J., Ahring, K., Beblo, S., Belanger-Quintana, A., Burlina, A., Campistol,
J., Coskun, T., Feillet, F., Gizewska, M., Huijbregts, S. C., Leuzzi, V., Maillot, F., Muntau, A. C., Rocha, J.
C., Romani, C., Trefz, F., & van Spronsen, F. J. (2020). PKU dietary handbook to accompany PKU
guidelines (vol 15, 171, 2020). Orphanet journal of rare diseases, 15(1), [230].
https://doi.org/10.1186/s13023-020-01486-6
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CORRECTION
Open Access
Correction to: PKU dietary handbook to
accompany PKU guidelines
A. MacDonald
1, A. M. J. van Wegberg
2, K. Ahring
3, S. Beblo
4, A. Bélanger-Quintana
5, A. Burlina
6, J. Campistol
7,
T. Co
şkun
8, F. Feillet
9, M. Gi
żewska
10, S. C. Huijbregts
11, V. Leuzzi
12, F. Maillot
13, A. C. Muntau
14, J. C. Rocha
15,
C. Romani
16, F. Trefz
17and F. J. van Spronsen
2*Correction to: Orphanet J Rare Dis 15, 171 (2020)
https://doi.org/10.1186/s13023-020-01391-y
The original article [
1
] contained an error in the Sport
and Nutrition
section of the manuscript whereby it was
stated that:
‘Approximately 20–30 g of protein equivalent from
protein substitute should be ingested post exercise.’
This sentence should instead have stated
‘ … 20g of
protein equivalent from protein substitute
… ’ which has
since been implemented in the original article.
Author details
1Dietetic Department, Birmingham Children’s Hospital, Birmingham, UK. 2Division of Metabolic Diseases, Beatrix Children’s Hospital, University Medical
Centre Groningen, University of Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.3Department of PKU, Kennedy Centre, Glostrup,
Denmark.4Department of Women and Child Health, Center for Pediatric
Research Leipzig, Hospital for Children and Adolescents, University Hospitals, Leipzig, Germany.5Department of Paediatrics, Hospital Ramon y Cajal
Madrid, Metabolic Diseases Unit, Madrid, Spain.6Division of Inherited
Metabolic Diseases, Department of Paediatrics, University Hospital of Padova, Padova, Italy.7Neuropaediatrics Department, Hospital Sant Joan de Déu,
Universitat de Barcelona, Barcelona, Spain.8Hacettepe University Faculty of
Medicine, Ankara, Turkey.9Department of Paediatrics, Hôpital d’Enfants
Brabois, CHU Nancy, Vandoeuvre les Nancy, France.10Department of
Paediatrics, Endocrinology, Diabetology, Metabolic Diseases and Cardiology of the Developmental Age, Pomeranian Medical University, Szczecin, Poland.
11Department of Clinical Child and Adolescent Studies-Neurodevelopmental
Disorders, Faculty of Social Sciences, Leiden University, Leiden, The Netherlands.12Department of Paediatrics, Child Neurology and Psychiatry,
Sapienza University of Rome, Via dei Sabelli 108, 00185 Rome, Italy.13CHRU
de Tours, Université François Rabelais, INSERM U1069, Tours, France.
14University Children’s Hospital, University Medical Centre
Hamburg-Eppendorf, 20246 Hamburg, Germany.15Nutrition & Metabolism,
NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisbon, Portugal. Centre for Health Technology and Services Research (CINTESIS), Porto, Portugal.16School of Life and Health Sciences, Aston
University, Birmingham, UK.17Department of Paediatrics, University of
Heidelberg, Heidelberg, Germany.
Reference
1. MacDonald A, et al. PKU dietary handbook to accompany PKU guidelines. Orphanet J Rare Dis. 2020;15:171 https://doi.org/10.1186/s13023-020-01391-y.
© The Author(s). 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
The original article can be found online at https://doi.org/10.1186/s13023-020-01391-y.
* Correspondence:f.j.van.spronsen@umcg.nl
2Division of Metabolic Diseases, Beatrix Children’s Hospital, University Medical
Centre Groningen, University of Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands
Full list of author information is available at the end of the article
MacDonaldet al. Orphanet Journal of Rare Diseases (2020) 15:230 https://doi.org/10.1186/s13023-020-01486-6