WHO 2016 classification: changes and advancements in the diagnosis of miscellaneous primary CNS tumours-Reference-Cited by-同舟云学术

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WHO 2016 classification: changes and advancements in the diagnosis of miscellaneous primary CNS tumours

Published:2018-02 Issue:2 Volume:44 Page:163-171
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Sahm F.¹,Reuss D. E.¹,Giannini C.²

Affiliation:

1. Department of Neuropathology; Institute of Pathology; Ruprecht-Karls-Universität Heidelberg; Heidelberg Germany

2. Division of Anatomic Pathology; Department of Laboratory Medicine and Pathology; Mayo Clinic; Rochester MN USA

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/nan.12397/fullpdf

Reference46 articles.

1. The effect of surgical margins on outcomes for low grade MPNSTs and atypical neurofibroma;Bernthal;J Surg Oncol,2014

2. Neurofibromin specific antibody differentiates malignant peripheral nerve sheath tumors (MPNST) from other spindle cell neoplasms;Reuss;Acta Neuropathol,2014

3. Methylation-based classification of benign and malignant peripheral nerve sheath tumors;Rohrich;Acta Neuropathol,2016

4. Loss of H3K27me3 expression is a highly sensitive marker for sporadic and radiation-induced MPNST;Prieto-Granada;Am J Surg Pathol,2016

5. Loss of H3K27 trimethylation distinguishes malignant peripheral nerve sheath tumors from histologic mimics;Schaefer;Mod Pathol,2016

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