Role of Electron Microscopy in the Diagnosis of Cadasil Syndrome: A Study of 32 Patients

BACKGROUND AND PURPOSE: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by NOTCH3 gene mutations that result in vascular smooth muscle cell (VSMC) degeneration. Its distinctive feature by electron microscopy (EM) is granular osmiophilic...

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Bibliografiske detaljer
Main Authors: Morroni, Manrico, Marzioni, Daniela, Ragno, Michele, Di Bella, Paolo, Cartechini, Elisabetta, Pianese, Luigi, Lorenzi, Teresa, Castellucci, Mario, Scarpelli, Marina
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2013
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3684609/
https://ncbi.nlm.nih.gov/pubmed/23799017
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0065482
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