Multiple craniospinal tumors in a pediatric patient with neurofibromatosis type 2: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00381-022-05531-6.pdf
Reference21 articles.
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2. Evans DG, Moran A, King A, Saeed S, Gurusinghe N, Ramsden R (2005) Incidence of vestibular schwannoma and neurofibromatosis 2 in the North West of England over a 10-year period: higher incidence than previously thought. Otol Neurotol 26(1):93–97
3. Petrilli AM, Fernandez-Valle C (2016) Role of merlin/NF2 inactivation in tumor biology. Oncogene 35(5):537–548
4. Seizinger BR, Martuza RL, Gusella JF (1986) Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma. Nature 322(6080):644–647
5. Trofatter JA, MacCollin MM, Rutter JL, Murrell JR, Duyao MP, Parry DM (1993) A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell 72(5):791–800
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