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Article

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

6 Nov 2011

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22057234
DOI: 10.1038/ng.1004

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromePMID 22057234Read ↗

Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2Semantic proximity Read ↗

Somatic IDH1 variant (p.R132C) in an adult male with Maffucci syndrome.Semantic proximity Read ↗

IDH1 R132C and ERC2 L309I Mutations Contribute to the Development of Maffucci's Syndrome.Semantic proximity Read ↗

An intermediate phenotype in IDH related enchondromatosis spectrum.Semantic proximity Read ↗

A case of Maffucci syndrome with a buccal hemangioma harboring a mutation in IDH1.Semantic proximity Read ↗

R132C IDH1 mutations are found in spindle cell hemangiomas and not in other vascular tumors or malformations.Semantic proximity Read ↗

Common Somatic Alterations Identified in Maffucci Syndrome by Molecular KaryotypingSemantic proximity Read ↗

Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndromeSemantic proximity Read ↗

Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia.Semantic proximity Read ↗

Maffucci syndrome: a genome-wide analysis using high resolution single nucleotide polymorphism and expression arrays on four cases.Semantic proximity Read ↗

Maffucci Syndrome Complicated by Giant Chondrosarcoma in the Left Ankle with an IDH1 R132C Mutation: Case ReportSemantic proximity Read ↗

[Spindle cell hemangioma: a clinicopathological and molecular analysis of eight cases].Semantic proximity Read ↗

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