Peripheral nerve sheath tumors in Neurofibromatosis Type 2: Surgical and histopathologic features
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Surgery
Reference14 articles.
1. A clinical study of type 2 neurofibromatosis;Evans;Q. J. Med.,1992
2. Clinicopathological variables of sporadic schwannomas of peripheral nerve in 291 patients and expression of biologically relevant markers;Young;J. Neurosurg.,2018
3. Tumors displaying hybrid schwannoma and neurofibroma features in patients with neurofibromatosis type 2;Montgomery;Clin. Neuropathol.,2016
4. Hybrid Neurofibroma/schwannoma is overrepresented among schwannomatosis and neurofibromatosis patients;Harder;Am. J. Surg. Pathol.,2012
5. Molecular analysis of hybrid neurofibroma/schwannoma identifies common monosomy 22 and α-T-catenin/CTNNA3 as a novel candidate tumor suppressor;Stahn;Am. J. Pathol.,2016
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