Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene

Multiple familial meningiomas occur in rare genetic syndromes, particularly neurofibromatosis type 2. The association of meningiomas and cerebral cavernous malformations (CCMs) has been reported in few patients in the medical literature. The purpose of our study is to corroborate a preferential asso...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Neuroradiol J
Prif Awduron: Garaci, Francesco, Marsili, Luisa, Riant, Florence, Marziali, Simone, Cécillon, Michaelle, Pasquarelli, Roberto, Sangiuolo, Federica, Floris, Roberto, Novelli, Giuseppe, Tournier-Lasserve, Elisabeth, Brancati, Francesco
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: SAGE Publications 2015
Pynciau:
Neoplastic Disease
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4757286/
https://ncbi.nlm.nih.gov/pubmed/26246098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1971400915591688
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