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Peer Review reports

From: Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature

Original Submission
1 Mar 2017 Submitted Original manuscript
13 Apr 2017 Reviewed Reviewer Report - Charlotte Opitz
19 Apr 2017 Reviewed Reviewer Report - Thomas Präger
20 Apr 2017 Reviewed Reviewer Report - Jaap Maltha
11 May 2017 Author responded Author comments - Karim Elhennawy
Resubmission - Version 2
11 May 2017 Submitted Manuscript version 2
12 Jun 2017 Reviewed Reviewer Report - Thomas Präger
28 Jun 2017 Author responded Author comments - Karim Elhennawy
Resubmission - Version 3
28 Jun 2017 Submitted Manuscript version 3
7 Jul 2017 Author responded Author comments - Karim Elhennawy
Resubmission - Version 4
7 Jul 2017 Submitted Manuscript version 4
Publishing
11 Jul 2017 Editorially accepted
15 Aug 2017 Article published 10.1186/s13256-017-1387-z

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Journal of Medical Case Reports

ISSN: 1752-1947