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Peer Review reports

From: Atypical haemolytic uremic syndrome with refractory multiorgan involvement and heterozygous CFHR1/CFHR3 gene deletion

Original Submission
6 Apr 2022 Submitted Original manuscript
14 Apr 2022 Reviewed Reviewer Report
25 Apr 2022 Reviewed Reviewer Report
8 May 2022 Reviewed Reviewer Report - Mathieu Lemaire
7 Aug 2022 Author responded Author comments - Jason Diep
Resubmission - Version 2
7 Aug 2022 Submitted Manuscript version 2
8 Aug 2022 Reviewed Reviewer Report
13 Aug 2022 Reviewed Reviewer Report
22 Aug 2022 Reviewed Reviewer Report - Mathieu Lemaire
17 Feb 2023 Author responded Author comments - Jason Diep
Resubmission - Version 3
17 Feb 2023 Submitted Manuscript version 3
21 Feb 2023 Reviewed Reviewer Report
6 Mar 2023 Reviewed Reviewer Report - Mathieu Lemaire
15 Mar 2023 Author responded Author comments - Jason Diep
Resubmission - Version 4
15 Mar 2023 Submitted Manuscript version 4
20 Mar 2023 Reviewed Reviewer Report - Mathieu Lemaire
Resubmission - Version 5
Submitted Manuscript version 5
Publishing
28 Mar 2023 Editorially accepted
5 May 2023 Article published 10.1186/s12882-023-03153-x

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