কিউআর কোড

Natural history of familial cerebral cavernous malformations: the CCM_Italia cohort study

BackgroundFamilial cerebral cavernous malformations (fCCMs) are a rare genetic autosomal dominant cerebrovascular disease characterized by multiple cerebral and spinal angiomas. The condition is caused by mutations in KRIT1 (CCM1), CCM2 (malcavernin), or PDCD10 (CCM3) and may lead to intracerebral h...

সম্পূর্ণ বিবরণ

সংরক্ষণ করুন:
প্রধান লেখক: Silvia Lanfranconi, Elisa Scola, Deborah Novelli, Anna Poggesi, Francesca Pescini, Marco Pavanello, Ferruccio Romano, Quintino Giorgio D’Alessandris, Walter Marani, Francesco Signorelli, Giorgio Iaconetta, Giovanni Torelli, Enrico Fainardi, Mariasavina Severino, Luigi Gianmaria Remore, Giulio Andrea Bertani, Giorgio Conte, Valeria Capra, Antonella Vasamì, Enrico Nicolis, Giorgia Contino, Dario Ronchi, Maria Chiara Palmieri, Alessandra Previtali, Pier Paolo Mattogno, Carmelo Lucio Sturiale, Maria Elena Solarino, Rita Caliulo, Maria Teresa Bozzi, Filippo Fratini, Elisa R. Zanier, Roberto Latini, Jennifer Marie Theresia Anna Meessen, Marco Locatelli, and the CCM_Italia investigators
বিন্যাস: Artigo
ভাষা:Inglês
প্রকাশিত: Frontiers Media S.A. 2026-01-01
মালা:Frontiers in Neurology
বিষয়গুলি:
cerebral cavernous malformation
familial cerebral cavernous malformation
intracerebral heamorrhage
focal neurological deficit
registry
অনলাইন ব্যবহার করুন:https://www.frontiersin.org/articles/10.3389/fneur.2025.1668098/full
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