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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...
Autores principales: | Morroni, Manrico, Marzioni, Daniela, Ragno, Michele, Di Bella, Paolo, Cartechini, Elisabetta, Pianese, Luigi, Lorenzi, Teresa, Castellucci, Mario, Scarpelli, Marina |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684609/ https://www.ncbi.nlm.nih.gov/pubmed/23799017 http://dx.doi.org/10.1371/journal.pone.0065482 |
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