Open Access

Erratum to: Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders

  • Linda Cassis1,
  • Elisenda Cortès-Saladelafont1,
  • Marta Molero-Luis1,
  • Delia Yubero1,
  • Maria Julieta González1,
  • Aida Ormazábal1,
  • Carme Fons1,
  • Cristina Jou1,
  • Cristina Sierra1,
  • Esperanza Castejon Ponce1,
  • Federico Ramos1,
  • Judith Armstrong1,
  • M. Mar O’Callaghan1,
  • Mercedes Casado1,
  • Raquel Montero1,
  • Silvia Meavilla-Olivas1,
  • Rafael Artuch1,
  • Ivo Barić2,
  • Franco Bartoloni3,
  • Cinzia Maria Bellettato4,
  • Fedele Bonifazi3,
  • Adriana Ceci3,
  • Ljerka Cvitanović-Šojat2,
  • Christine I. Dali5,
  • Francesca D’Avanzo4,
  • Ksenija Fumic2,
  • Viviana Giannuzzi3,
  • Christina Lampe4, 6,
  • Maurizio Scarpa4, 6, 7 and
  • Ángels Garcia-Cazorla1Email author
Contributed equally
Orphanet Journal of Rare Diseases201611:147

https://doi.org/10.1186/s13023-016-0431-1

Received: 18 April 2016

Accepted: 18 April 2016

Published: 3 November 2016

The original article was published in Orphanet Journal of Rare Diseases 2015 10:164

Erratum

Unfortunately, the original version of this article [1] contained an error. The author list displayed the following author names incorrectly. Aida Ormazábal was listed as Aida Ormazabal Herrero, Silvia Meavilla-Olivas as Silvia Maria Meavilla Olivas and Ángels Garcia-Cazorla as Ángels Garcia- Cazorla. This has been corrected in the original article and can also be seen correctly above.

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

Authors’ Affiliations

(1)
Neurology, gastroenterology pathology and clinical biochemistry Departments, IRP-HSJD and CIBERER
(2)
Department of Pediatrics, University Hospital Center Zagreb, Zagreb & University of Zagreb, School of Medicine
(3)
Gianni Benzi Pharmacological Research Foundation
(4)
Department of Women and Children Health, Brains for Brain Foundation
(5)
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet
(6)
Department of Pediatric and Adolescent Medicine, Centre for Rare Diseases, Horst Schmidt Klinik Wiesbaden
(7)
Department of Women’s and Children’s Health, University of Padova

Reference

  1. Cassis L, Cortès-Saladelafont E, Molero-Luis M, Yubero D, González MJ, Ormazábal A, et al. Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders. Orphanet J Rare Dis. 2015;10:164.View ArticlePubMedPubMed CentralGoogle Scholar

Copyright

© Cassis et al. 2016

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