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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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Main Authors: Kobayashi, Atsushi, Matsuura, Yuichi, Mohri, Shirou, Kitamoto, Tetsuyuki
Formáid: Artigo
Teanga:Inglês
Foilsithe: BioMed Central 2014
Ábhair:
Rochtain Ar Líne: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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