Skip to main content

Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema

  • The original article was published in Orphanet Journal of Rare Diseases 2020 15:221

Correction to: Orphanet Journal of Rare Diseases (2020) 15:221 https://doi.org/10.1186/s13023-020-01506-5

In the original version of this article [1], the affiliations of authors Holger Gothe and Anja Lachmann were unfortunately interchanged:

Dr. Gothe was erroneously presented as affiliated with the Shire Deutschland GmbH, while Dr. Lachmann as affiliated with the Chair for Health Sciences/Public Health, Medical Faculty "Carl Gustav Carus", Technical University Dresden.

The correct authors’ affiliations are shown here below and are included in the ‘Author details’ section of this Correction. These have already been corrected in the original article.

Holger Gothe2,3,4

2 IGES Institut GmbH, Friedrichstraße 180, 10117 Berlin, Germany.

3 Chair for Health Sciences / Public Health, Medical Faculty "Carl Gustav Carus", Technical University Dresden, Loescherstrasse 18, 01307 Dresden, Germany.

4 Institute of Public Health, Medical Decision Making and Health Technology Assessment, Department of Public Health, Health Services Research and Health Technology Assessment, UMIT – University for Health Sciences, Medical Informatics and Technology, Eduard Wallnoefer Zentrum 1, A-6060 Hall in Tirol, Austria.

Anja Lachmann 5.

5 Shire Deutschland GmbH, Friedrichstraße 149, 10117 Berlin, Germany.

Reference

  1. 1.

    Magerl et al. A Germany-wide survey study on the patient journey of patients with hereditary angioedema. Orphanet J Rare Diseases. 2020;15:221. https://doi.org/10.1186/s13023-020-01506-5.

Download references

Author information

Affiliations

Authors

Corresponding author

Correspondence to Holger Gothe.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

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, visit http://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.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Magerl, M., Gothe, H., Krupka, S. et al. Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema. Orphanet J Rare Dis 16, 97 (2021). https://doi.org/10.1186/s13023-021-01714-7

Download citation