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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Detalles Bibliográficos
Autores principales: Spilberg, Gabriela, Marchiori, Edson, Gasparetto, Emerson L, Cabral, Rafael Ferracini, Takayassu, Tatiana Chinem, Batista, Raquel Ribeiro, Vieira, Isabela Garcia
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740231/
https://www.ncbi.nlm.nih.gov/pubmed/19829851
http://dx.doi.org/10.4076/1757-1626-2-6720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740231/
https://www.ncbi.nlm.nih.gov/pubmed/19829851
http://dx.doi.org/10.4076/1757-1626-2-6720

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