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Peer Review reports

From: A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Original Submission
10 Apr 2008 Submitted Original manuscript
10 Apr 2008 Author responded Author comments - Khaled Abu-Amero
Resubmission - Version 2
10 Apr 2008 Submitted Manuscript version 2
6 May 2008 Author responded Author comments - Khaled Abu-Amero
Resubmission - Version 3
6 May 2008 Submitted Manuscript version 3
20 Nov 2008 Reviewed Reviewer Report - Michael Freilinger
19 Dec 2008 Reviewed Reviewer Report - Bernhard Schaller
22 Dec 2008 Author responded Author comments - Khaled Abu-Amero
Resubmission - Version 4
22 Dec 2008 Submitted Manuscript version 4
24 Jan 2009 Author responded Author comments - Khaled Abu-Amero
Resubmission - Version 5
24 Jan 2009 Submitted Manuscript version 5
Publishing
15 Oct 2009 Editorially accepted
15 Oct 2009 Article published 10.1186/1752-1947-3-77

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Journal of Medical Case Reports

ISSN: 1752-1947