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...

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Vydáno v:Neuroradiol J
Hlavní autoři: Garaci, Francesco, Marsili, Luisa, Riant, Florence, Marziali, Simone, Cécillon, Michaelle, Pasquarelli, Roberto, Sangiuolo, Federica, Floris, Roberto, Novelli, Giuseppe, Tournier-Lasserve, Elisabeth, Brancati, Francesco
Médium: Artigo
Jazyk:Inglês
Vydáno: SAGE Publications 2015
Témata:
Neoplastic Disease
On-line přístup: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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