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Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Orphanet Journal of Rare Diseases volume 14, Article number: 199 (2019) Cite this article

The Original Article was published on 05 September 2018

Correction to: Orphanet J Rare Dis (2018) 13:155.

https://doi.org/10.1186/s13023-018-0889-0

The original version of this article [1] unfortunately included an error to an author’s name. Author Jordi Díaz-Manera was erroneously presented as Jorge Alberto Diaz Manera. The correct author name has been included in the author list of this Correction article.

For citation purposes the author’s given name is Jordi and family name Díaz-Manera. Therefore, the correct citation of the author’s details is: Díaz-Manera J.

Reference

  1. Wood L, et al. Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease. Orphanet J Rare Dis. 2018;13(155). https://doi.org/10.1186/s13023-018-0889-0.

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Authors and Affiliations

  1. Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK

    Libby Wood & Aura Cecilia Jimenez-Moreno

  2. Centre de Référence des Maladies Neuromusculaires, Hôpital Henri Mondor, Paris, France

    Guillaume Bassez & Celine Dogan

  3. Scientific Institute of Public Health, Brussels, Belgium

    Corinne Bleyenheuft

  4. Western University, London, Canada

    Craig Campbell

  5. Centre de recherche du CHU de Québec, Université Laval, Quebec, Canada

    Louise Cossette & Jack Puymirat

  6. Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China

    Yi Dai

  7. Office of Population Health Genomics, Perth, Western Australia

    Hugh Dawkins & Caroline Graham

  8. Neuromuscular disorders Unit, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain

    Jordi Díaz-Manera

  9. Neuromuscular & Neuro-genetics Unit, Air Hospital, Cairo, Egypt

    Rasha el Sherif

  10. U.O. Neurology and Stroke Unit, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy

    Barbara Fossati & Giovani Meola

  11. Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA

    James Hilbert & Elizabeth Luebbe

  12. Department of Neurology, Alexandrovska University Hospital, Medical University, Sofia, Bulgaria

    Kristinia Kastreva & Ivailo Tournev

  13. Department of Promoting Clinical Trial and Translational Medicine, National Center for Neurology and Psychiatry, Translational Medical Center, Kodaira, Japan

    En Kimura

  14. University of Calgary, Calgary, Canada

    Lawrence Korngut

  15. Department of Neurology, Medical University of Warsaw, Warszawa, Poland

    Anna Kostera-Pruszczyk & Anna Lusakowska

  16. University Hospital Örebro, Örebro, Sweden

    Christopher Lindberg & Bjorn Lindvall

  17. University Hospital Prague- Motol and Charles University Prague, Prague, Czech Republic

    Radim Mazanec

  18. Muscular Dystrophy Association, Chicago, USA

    Liannna Orlando

  19. Department of Functional Diagnostic Science, Osaka University Graduate School of Medicine, Suita, Japan

    Masanori P. Takahashi

  20. Neurology Clinic, School of Medicine, University of Belgrade, Belgrade, Serbia

    Stojan Peric & Vidosava Rakocevic-Stojanovic

  21. Neurology, Auckland City Hospital, Private Bag 92024, Auckland, 1142, New Zealand

    Miriam Rodrigues & Richard Roxburgh

  22. Department of Neurology, Friedrich-Baur-Institute, Klinikum München, Munich, Germany

    Benedikt Schoser & Simone Thiele

  23. Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Valencia, Spain

    Sonia Segovia

  24. Psychiatry and Narcology, Academy of medical science of Ukraine, Institute of Neurology, Kharkiv, Ukraine

    Andriy Shatillo

  25. Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

    Baziel van Engelen

  26. University Hospital and Masaryk University Brno, Brno, Czech Republic

    Stanislav Vohanka

  27. Department of Neuropediatrics and Muscle Disorders, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany

    Hanns Lochmüller

  28. Centro Nacional de Análisis Genómico (CNAG-CRG), Center for Genomic Regulation, Barcelona Institute of Science and Technology (BIST), Barcelona, Spain

    Hanns Lochmüller

Authors
  1. Libby Wood
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  2. Guillaume Bassez
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  3. Corinne Bleyenheuft
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  4. Craig Campbell
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  5. Louise Cossette
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  6. Aura Cecilia Jimenez-Moreno
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  7. Yi Dai
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  8. Hugh Dawkins
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  9. Jordi Díaz-Manera
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  10. Celine Dogan
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  11. Rasha el Sherif
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  12. Barbara Fossati
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  13. Caroline Graham
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  14. James Hilbert
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  15. Kristinia Kastreva
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  16. En Kimura
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  17. Lawrence Korngut
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  18. Anna Kostera-Pruszczyk
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  19. Christopher Lindberg
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  20. Bjorn Lindvall
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  21. Elizabeth Luebbe
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  22. Anna Lusakowska
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  23. Radim Mazanec
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  24. Giovani Meola
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  25. Liannna Orlando
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  26. Masanori P. Takahashi
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  27. Stojan Peric
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  28. Jack Puymirat
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  29. Vidosava Rakocevic-Stojanovic
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  30. Miriam Rodrigues
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  31. Richard Roxburgh
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  32. Benedikt Schoser
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  33. Sonia Segovia
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  34. Andriy Shatillo
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  35. Simone Thiele
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  36. Ivailo Tournev
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  37. Baziel van Engelen
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  38. Stanislav Vohanka
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  39. Hanns Lochmüller
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Corresponding author

Correspondence to Libby Wood.

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Wood, L., Bassez, G., Bleyenheuft, C. et al. Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease. Orphanet J Rare Dis 14, 199 (2019). https://doi.org/10.1186/s13023-019-1157-7

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  • DOI: https://doi.org/10.1186/s13023-019-1157-7

Orphanet Journal of Rare Diseases

ISSN: 1750-1172