Variation in recruitment across sites in a consent-based clinical data registry: lessons from the Canadian Stroke Network
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* Corresponding author: Donald J Willison willison@mcmaster.ca
BMC Medical Ethics 2006, 7:6 doi:10.1186/1472-6939-7-6
Pre-publication versions of this article and reviewers' reports
| Original Submission - Version 1 | Manuscript | 16 Dec 2005 | |
| Reviewer's Report | Helen Aveyard | 17 Jan 2006 | |
| Reviewer's Report | Gerald Schatz | 07 Feb 2006 | |
| Resubmission - Version 2 | Manuscript | Author's comment | 15 Mar 2006 |
| Reviewer's Report | Gerald Schatz | 23 Mar 2006 | |
| Reviewer's Report | Helen Aveyard | 31 Mar 2006 | |
| Resubmission - Version 3 | Manuscript | Author's comment | 13 Apr 2006 |
| Reviewer's Report | Gerald Schatz | 25 Apr 2006 | |
| Reviewer's Report | Helen Aveyard | 28 Apr 2006 | |
| Resubmission - Version 4 | Manuscript | Author's comment | 05 May 2006 |
| Editorial acceptance | 05 May 2006 | ||
| Published | 23 May 2006 |