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

Orphanet Journal of Rare Diseases volume 11, Article number: 147 (2016) Cite this article

The Original Article was published on 30 December 2015

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.

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.

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Author notes

    Authors and Affiliations

    1. Neurology, gastroenterology pathology and clinical biochemistry Departments, IRP-HSJD and CIBERER, Barcelona, Spain

      Linda Cassis, Elisenda Cortès-Saladelafont, Marta Molero-Luis, Delia Yubero, Maria Julieta González, Aida Ormazábal, Carme Fons, Cristina Jou, Cristina Sierra, Esperanza Castejon Ponce, Federico Ramos, Judith Armstrong, M. Mar O’Callaghan, Mercedes Casado, Raquel Montero, Silvia Meavilla-Olivas, Rafael Artuch & Ángels Garcia-Cazorla

    2. Department of Pediatrics, University Hospital Center Zagreb, Zagreb & University of Zagreb, School of Medicine, Zagreb, Croatia

      Ivo Barić, Ljerka Cvitanović-Šojat & Ksenija Fumic

    3. Gianni Benzi Pharmacological Research Foundation, Valenzano, BA, Italy

      Franco Bartoloni, Fedele Bonifazi, Adriana Ceci & Viviana Giannuzzi

    4. Department of Women and Children Health, Brains for Brain Foundation, Padova, Italy

      Cinzia Maria Bellettato, Francesca D’Avanzo, Christina Lampe & Maurizio Scarpa

    5. Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark

      Christine I. Dali

    6. Department of Pediatric and Adolescent Medicine, Centre for Rare Diseases, Horst Schmidt Klinik Wiesbaden, Wiesbaden, Germany

      Christina Lampe & Maurizio Scarpa

    7. Department of Women’s and Children’s Health, University of Padova, Padova, Italy

      Maurizio Scarpa

    Authors
    1. Linda Cassis
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    2. Elisenda Cortès-Saladelafont
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    3. Marta Molero-Luis
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    4. Delia Yubero
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    5. Maria Julieta González
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    6. Aida Ormazábal
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    7. Carme Fons
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    8. Cristina Jou
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    10. Esperanza Castejon Ponce
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    11. Federico Ramos
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    12. Judith Armstrong
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    13. M. Mar O’Callaghan
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    14. Mercedes Casado
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    15. Raquel Montero
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    16. Silvia Meavilla-Olivas
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    17. Rafael Artuch
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    18. Ivo Barić
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    19. Franco Bartoloni
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    20. Cinzia Maria Bellettato
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    21. Fedele Bonifazi
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    22. Adriana Ceci
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    23. Ljerka Cvitanović-Šojat
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    24. Christine I. Dali
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    25. Francesca D’Avanzo
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    26. Ksenija Fumic
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    27. Viviana Giannuzzi
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    28. Christina Lampe
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    29. Maurizio Scarpa
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    30. Ángels Garcia-Cazorla
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    Corresponding author

    Correspondence to Ángels Garcia-Cazorla.

    Additional information

    The online version of the original article can be found under doi:10.1186/s13023-015-0376-9.

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    Cite this article

    Cassis, L., Cortès-Saladelafont, E., Molero-Luis, M. et al. Erratum to: Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders. Orphanet J Rare Dis 11, 147 (2016). https://doi.org/10.1186/s13023-016-0431-1

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

    Orphanet Journal of Rare Diseases

    ISSN: 1750-1172