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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Hauptverfasser: Spilberg, Gabriela, Marchiori, Edson, Gasparetto, Emerson L, Cabral, Rafael Ferracini, Takayassu, Tatiana Chinem, Batista, Raquel Ribeiro, Vieira, Isabela Garcia
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2009
Schlagworte:
Research article
Online Zugang: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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