Magnetic resonance findings of neurofibromatosis type 2: a case report

Neurofibromatosis type 2 is an inherited autosomal dominant syndrome, characterized by multiple neoplasms of the central and peripheral nervous system associated with ocular abnormalities. The most common tumor associated with the disease is the vestibulocochlear schwannoma (VIII cranial nerve), and...

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Autori principali: Spilberg, Gabriela, Marchiori, Edson, Gasparetto, Emerson L, Cabral, Rafael Ferracini, Takayassu, Tatiana Chinem, Batista, Raquel Ribeiro, Vieira, Isabela Garcia
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2009
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Research article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2740231/
https://ncbi.nlm.nih.gov/pubmed/19829851
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4076/1757-1626-2-6720
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