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Peer Review reports

From: Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS) - registry Swabia

Original Submission
2 Oct 2012 Submitted Original manuscript
22 Oct 2012 Author responded Author comments - Gabriele Nagel
Resubmission - Version 2
22 Oct 2012 Submitted Manuscript version 2
14 Dec 2012 Author responded Author comments - Gabriele Nagel
Resubmission - Version 3
14 Dec 2012 Submitted Manuscript version 3
Publishing
6 Feb 2013 Editorially accepted
17 Feb 2013 Article published 10.1186/1471-2377-13-22

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BMC Neurology

ISSN: 1471-2377

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