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Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome

Orphanet Journal of Rare Diseases volume 16, Article number: 145 (2021) Cite this article

The Original Article was published on 12 August 2020

Correction to: Orphanet J Rare Dis (2020) 15:206 https://doi.org/10.1186/s13023-020-01493-7

The original version of this article [1] unfortunately included a typo to a co-author’s name.

Author Carola Reinhard was erroneously presented as Carola Rheinard.

The correct author name is shown in the author list of this Correction and has already been updated in the original article.

Reference

  1. Atalaia, et al. A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome. Orphanet J Rare Dis. 2020;15:206. https://doi.org/10.1186/s13023-020-01493-7.

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Author information

Authors and Affiliations

  1. Sorbonne Universite - Inserm UMRS 974, Center of Research in Myology, Institut de Myologie, G.H. Pitié-Salpêtrière Paris, 47, boulevard de l’Hopital, 75 651, Paris Cedex 13, France

    Antonio Atalaia, Bertrand Fontaine, Rabah Ben Yaou & Gisèle Bonne

  2. Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada

    Rachel Thompson & Hanns Lochmuller

  3. CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain

    Alberto Corvo, Davide Piscia, Leslie Matalonga, Carles Hernandez-Ferrer, Steven Laurie, Hanns Lochmuller & Sergi Beltran

  4. The Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA

    Leigh Carmody & Peter Robinson

  5. Paediatric Neurology, Vall D’Hebron University Hospital and VHIR (Euro-NMD, ERN-RND), 08035, Barcelona, Spain

    Alfons Macaya & David Gómez-Andrés

  6. Department of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK

    Angela Lochmuller, Katherine Schon, Matthew J. Jennings & Rita Horvath

  7. Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany

    Birte Zurek, Carola Reinhard, Olaf Riess & Holm Graessner

  8. Department of Biomedical Sciences and Human Oncology, School of Medicine, University of Bari Aldo Moro, Bari, Italy

    Jean-François Desaphy

  9. Institute of Neurogenetics, University of Lübeck, 23538, Lübeck, Germany

    Katja Lohmann

  10. Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany

    Matthis Synofzik

  11. German Center for Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, Germany

    Matthis Synofzik

  12. Unité de Morphologie Neuromusculaire, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France

    Teresinha Evangelista

  13. Sorbonne Université, AP-HP, INSERM, Centre de Référence Des Maladies Neuromusculaires Nord/Est, Ile de France, Paris, France

    Teresinha Evangelista

  14. Department of Paediatrics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, England

    Thiloka Ratnaike

  15. Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK

    Thiloka Ratnaike

  16. EURORDIS – Rare Diseases Europe, Paris, France

    Virginie Bros-Facer & Gulcin Gumus

  17. Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge and MRC Mitochondrial Biology Unit, Cambridge Biomedical Campus, Cambridge, UK

    Patrick Chinnery

  18. Department of Neuropediatrics and Muscle Disorders, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany

    Hanns Lochmuller

  19. Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, Canada

    Hanns Lochmuller

  20. Brain and Mind Research Institute, University of Ottawa, Ottawa, Canada

    Hanns Lochmuller

Authors
  1. Antonio Atalaia
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  2. Rachel Thompson
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  3. Alberto Corvo
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  4. Leigh Carmody
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  5. Davide Piscia
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  6. Leslie Matalonga
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  7. Alfons Macaya
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  8. Angela Lochmuller
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  9. Bertrand Fontaine
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  10. Birte Zurek
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  11. Carles Hernandez-Ferrer
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  12. Carola Reinhard
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  13. David Gómez-Andrés
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  14. Jean-François Desaphy
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  15. Katherine Schon
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  16. Katja Lohmann
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  17. Matthew J. Jennings
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  18. Matthis Synofzik
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  19. Olaf Riess
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  20. Rabah Ben Yaou
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  21. Teresinha Evangelista
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  22. Thiloka Ratnaike
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  23. Virginie Bros-Facer
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  24. Gulcin Gumus
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  25. Rita Horvath
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  26. Patrick Chinnery
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  27. Steven Laurie
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  28. Holm Graessner
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  29. Peter Robinson
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  30. Hanns Lochmuller
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  31. Sergi Beltran
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  32. Gisèle Bonne
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Corresponding author

Correspondence to Antonio Atalaia.

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Atalaia, A., Thompson, R., Corvo, A. et al. Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome. Orphanet J Rare Dis 16, 145 (2021). https://doi.org/10.1186/s13023-021-01777-6

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  • DOI: https://doi.org/10.1186/s13023-021-01777-6

Orphanet Journal of Rare Diseases

ISSN: 1750-1172