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Cerebrovascular Disease Progression in Patients With ACTA2 Arg179 Pathogenic Variants
OBJECTIVE: To establish progression of imaging biomarkers of stroke, arterial steno-occlusive disease, and white matter injury in patients with smooth muscle dysfunction syndrome caused by mutations in the ACTA2 gene, we analyzed 113 cerebral MRI scans from a retrospective cohort of 27 patients with...
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| Publicado no: | Neurology |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7905785/ https://ncbi.nlm.nih.gov/pubmed/33199432 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000011210 |
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