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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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Detalhes bibliográficos
Main Authors: Spilberg, Gabriela, Marchiori, Edson, Gasparetto, Emerson L, Cabral, Rafael Ferracini, Takayassu, Tatiana Chinem, Batista, Raquel Ribeiro, Vieira, Isabela Garcia
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2009
Assuntos:
Acesso em linha: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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