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Peer Review reports

From: The Swiss Multiple Sclerosis Registry (SMSR): study protocol of a participatory, nationwide registry to promote epidemiological and patient-centered MS research

Original Submission
27 Oct 2017 Submitted Original manuscript
1 May 2018 Author responded Author comments - Nina Steinemann
Resubmission - Version 2
1 May 2018 Submitted Manuscript version 2
17 Jul 2018 Author responded Author comments - Nina Steinemann
Resubmission - Version 3
17 Jul 2018 Submitted Manuscript version 3
Publishing
6 Aug 2018 Editorially accepted
13 Aug 2018 Article published 10.1186/s12883-018-1118-0

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