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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2011-5-27
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pubmed:abstractText |
The most common genetic predisposition to multiple schwannoma growth is mutation of the neurofibromatosis type 2 gene. We describe a patient with multiple schwannomas and mutation in the recently described INI1 gene, which also predisposes to the disease. We explore the implications for prognosis and outcome.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1360-046X
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
330-2
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pubmed:meshHeading |
pubmed-meshheading:20854059-Aged,
pubmed-meshheading:20854059-Chromosomal Proteins, Non-Histone,
pubmed-meshheading:20854059-DNA-Binding Proteins,
pubmed-meshheading:20854059-Genetic Predisposition to Disease,
pubmed-meshheading:20854059-Humans,
pubmed-meshheading:20854059-Magnetic Resonance Imaging,
pubmed-meshheading:20854059-Male,
pubmed-meshheading:20854059-Mutation,
pubmed-meshheading:20854059-Neurilemmoma,
pubmed-meshheading:20854059-Neurofibromatoses,
pubmed-meshheading:20854059-Neurofibromatosis 2,
pubmed-meshheading:20854059-Prognosis,
pubmed-meshheading:20854059-Skin Neoplasms,
pubmed-meshheading:20854059-Transcription Factors,
pubmed-meshheading:20854059-Treatment Outcome
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pubmed:year |
2011
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pubmed:articleTitle |
Multiple schwannomatosis caused by the recently described INI1 gene--molecular pathology, and implications for prognosis.
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pubmed:affiliation |
Department of Clinical Neurosciences, Western General Hospital, Edinburgh, UK. paul.brennan@ed.ac.uk
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pubmed:publicationType |
Journal Article,
Case Reports
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