Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literature

Peer Review reports

Original Submission
16 Jul 2015	Submitted	Original manuscript
24 Oct 2015	Reviewed	Reviewer Report - Carla BIzzarri
3 Nov 2015	Reviewed	Reviewer Report - Assunta Albanese
23 Nov 2015	Author responded	Author comments - Mirjana Kocova
Resubmission - Version 2
23 Nov 2015	Submitted	Manuscript version 2
Publishing
2 Dec 2015	Editorially accepted
15 Dec 2015	Article published	10.1186/s12902-015-0076-4

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