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Publikováno v:
Case Reports in Neurology, Vol 10, Iss 3, Pp 261-265 (2018)
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare, fatal human prion disease that is characterized by progressive dementia and neurologic degeneration. It can mimic multiple other neurological disorders, and a high index of clinical suspicion is ne
Externí odkaz:
https://doaj.org/article/6048f3feb81b46429e790050626c0415
Publikováno v:
Case Reports in Neurology
Case Reports in Neurology, Vol 10, Iss 3, Pp 261-265 (2018)
Case Reports in Neurology, Vol 10, Iss 3, Pp 261-265 (2018)
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare, fatal human prion disease that is characterized by progressive dementia and neurologic degeneration. It can mimic multiple other neurological disorders, and a high index of clinical suspicion is ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45f90655cd09e587056858a5fd813524
https://doi.org/10.1159/000492613
https://doi.org/10.1159/000492613
