Clinical features of spinal schwannomas in 65 patients with schwannomatosis compared with 831 with solitary schwannomas and 102 with neurofibromatosis Type 2: a retrospective study at a single institution

Prognostic value and management of spinal tumors in neurofibromatosis type 2 patients

(2013) Rabih Aboukais et al.   ACTA NEUROCHIRURGICA

Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria

(2013) Scott R. Plotkin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

(2013) Arkadiusz Piotrowski et al.   NATURE GENETICS

Intraosseous schwannoma in schwannomatosis

(2013) T. G. Kashima et al.   SKELETAL RADIOLOGY

Natural history of intradural–extramedullary spinal cord tumors

(2012) Hiroshi Ozawa et al.   ACTA NEUROLOGICA BELGICA

Clinical Features of Schwannomatosis: A Retrospective Analysis of 87 Patients

(2012) V. L. Merker et al.   ONCOLOGIST

Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis

(2011) Miriam J. Smith et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Schwannomatosis, sporadic schwannomatosis, and familial schwannomatosis: a surgical series with long-term follow-up

(2010) Augusto Gonzalvo et al.   JOURNAL OF NEUROSURGERY

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

(2009) Costanza Bacci et al.   NEUROGENETICS

Neurofibromatosis type 2 (NF2): A clinical and molecular review

(2009) D Gareth R Evans   Orphanet Journal of Rare Diseases

Microsurgical management of spinal schwannomas: evaluation of 128 cases

(2008) Sam Safavi-Abbasi et al.   JOURNAL OF NEUROSURGERY-SPINE

Evidence of a four-hit mechanism involvingSMARCB1andNF2in schwannomatosis-associated schwannomas

(2007) Roberta Sestini et al.   HUMAN MUTATION