Source:http://linkedlifedata.com/resource/pubmed/id/19349806
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2009-4-7
|
pubmed:abstractText |
Rosette-forming glioneuronal tumor is a rare, rather recently described tumor featuring a highly distinctive, biphasic histological pattern, including a cytologically uniform neuronal component of Homer-Wright type pseudorosettes and an accompanying astrocytic element resembling pilocytic astrocytoma. Its occurrence in the posterior fossa and association with the fourth ventricle is stereotypical and a feature of all reported cases.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
1524-4040
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
64
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
E771-2; discussion E772
|
pubmed:meshHeading |
pubmed-meshheading:19349806-Astrocytoma,
pubmed-meshheading:19349806-Humans,
pubmed-meshheading:19349806-Magnetic Resonance Imaging,
pubmed-meshheading:19349806-Male,
pubmed-meshheading:19349806-Neurofibromatosis 1,
pubmed-meshheading:19349806-Optic Chiasm,
pubmed-meshheading:19349806-Optic Nerve Neoplasms,
pubmed-meshheading:19349806-Young Adult
|
pubmed:year |
2009
|
pubmed:articleTitle |
Rosette-forming glioneuronal tumor: report of a chiasmal-optic nerve example in neurofibromatosis type 1: special pathology report.
|
pubmed:affiliation |
Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, Minnesota, USA. scheithauer.bernd@mayo.edu
|
pubmed:publicationType |
Journal Article,
Case Reports
|