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Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems
Dura mater graft-associated Creutzfeldt-Jakob disease (dCJD) can be divided into two subgroups that exhibit distinct clinical and neuropathological features, with the majority represented by a non-plaque-type of dCJD (np-dCJD) and the minority by a plaque-type of dCJD (p-dCJD). The two distinct phen...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3976164/ https://ncbi.nlm.nih.gov/pubmed/24685293 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2051-5960-2-32 |
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