Characteristics of gliomas in patients with somatic IDH mosaicism
Open Access
- 31 March 2016
- journal article
- research article
- Published by Springer Science and Business Media LLC in Acta Neuropathologica Communications
- Vol. 4 (1), 1-8
- https://doi.org/10.1186/s40478-016-0302-y
Abstract
No abstract availableKeywords
This publication has 51 references indexed in Scilit:
- Bone scintigraphy in Ollier′s disease: A rare case reportIndian Journal of Nuclear Medicine, 2013
- SNP Array Analysis Reveals Novel Genomic Abnormalities Including Copy Neutral Loss of Heterozygosity in Anaplastic OligodendrogliomasPLOS ONE, 2012
- Transformation by the (R)-enantiomer of 2-hydroxyglutarate linked to EGLN activationNature, 2012
- IDH1 mutation is sufficient to establish the glioma hypermethylator phenotypeNature, 2012
- IDH mutation impairs histone demethylation and results in a block to cell differentiationNature, 2012
- Multifocal intracranial astrocytoma in a pediatric patient with Ollier diseaseIndian Journal of Radiology and Imaging, 2012
- Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromeNature Genetics, 2011
- Diffuse gliomas in an adolescent with multiple enchondromatosis (Ollier’s disease)Oncology Letters, 2010
- Inherited predisposition to gliomaNeuro-Oncology, 2009
- IDH1andIDH2Mutations in GliomasThe New England Journal of Medicine, 2009