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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Detaylı Bibliyografya
Asıl Yazarlar: Spilberg, Gabriela, Marchiori, Edson, Gasparetto, Emerson L, Cabral, Rafael Ferracini, Takayassu, Tatiana Chinem, Batista, Raquel Ribeiro, Vieira, Isabela Garcia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2009
Konular:
Research article
Online Erişim: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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