Pediatric schwannomatosis, a rare but distinct form of neurofibromatosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology, Nuclear Medicine and imaging,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00247-015-3482-x.pdf
Reference8 articles.
1. MacCollin M, Woodfin W, Kronn D et al (1996) Schwannomatosis: a clinical and pathologic study. Neurology 46:1072–1079
2. Merker VL, Esparaza S, Smith MJ et al (2012) Clinical features of schwannomatosis: a retrospective analysis of 87 patients. Oncologist 17:1317–1322
3. Koontz NA, Wiens AL, Agarwal A et al (2013) Schwannomatosis: the overlooked neurofibromatosis? AJR Am J Roentgenol 200:w646–w653
4. Plotkin SR, Blakely JO, Evans DG et al (2013) Update from the 2011 International Schwannomatosis Workshop: from genetics to diagnostic criteria. Am J Med Genet 161:405–416
5. Piotrowski A, Xie J, Liu YF et al (2014) Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. Nat Genet 46:182–187
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