Publications
| Title | Abstract | Year(sorted ascending) Filter | PMID Filter |
|---|
| [prion dementias: nosology and diagnostic difficulties in the spectrum of creutzfeld-jakob encephalopathy]. | creutzfeldt-jakob disease (cjd) is one form of subacute prion diseases with spongiform encephalopathy. hereditary, infectious and sporadic types of the disorder can be distinguished. the abnormal transformation of the prion protein, relevant in the normal synaptic transmission is considered as an important factor in the development of this disease. gerstmann-sträussler-scheinker syndrome (gss) and familial fatal insomnia (ffi) are the other diseases belonging to the same disease spectrum. the co ... | 1997 | 9157343 |