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Cerebral cavernous malformations as a disease of vascular permeability: from bench to bedside with caution
Tremendous insight into the molecular and genetic pathogenesis of cerebral cavernous malformations (CCMs) has been gained over the past 2 decades. This includes the identification of 3 distinct genes involved in familial CCMs. Still, a number of unanswered questions regarding the process from gene m...
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| Publicat a: | Neurosurg Focus |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6599630/ https://ncbi.nlm.nih.gov/pubmed/20809762 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3171/2010.5.FOCUS10121 |
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