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Open Access Pre-publication history

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

Gabriele Nagel*, Hatice Ünal, Angela Rosenbohm, Albert C Ludolph, Dietrich Rothenbacher and the ALS Registry Study Group

BMC Neurology 2013, 13:22  doi:10.1186/1471-2377-13-22

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 Manuscript 02 Oct 2012
Resubmission - Version 2 Manuscript Author's comment 22 Oct 2012
Resubmission - Version 3 Manuscript Author's comment 14 Dec 2012
Editor's comment Editor's comment 06 Feb 2013
Editorial acceptance 06 Feb 2013
Published 17 Feb 2013