Cargando…
A Rare Case of Histopathologically Confirmed Creutzfeldt–Jakob Disease from Romania, Long Route to Diagnosis—Case Report and an Overview of the Romanian CJD Situation
Creutzfeldt–Jacob disease is a progressive and ultimately fatal disease, representing one of the most common forms of prion diseases. It is a rare pathology presenting with various symptomatology, and the fact that a definite diagnosis can be obtained solely by neuropathological techniques makes it...
Autores principales: | Kelemen, Krisztina, Kövecsi, Attila, Banias, Laura, Klára, Izolda, Mihály, István, Forró, Csilla, Szász, József Attila, Szatmári, Szabolcs |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409679/ https://www.ncbi.nlm.nih.gov/pubmed/36013055 http://dx.doi.org/10.3390/jcm11164803 |
Ejemplares similares
-
The Various Faces of Creutzfeldt-Jakob Disease (CJD); a Case of CJD Presenting as Psychosis in a Middle-Aged Woman
por: Sodiya, Olusegun, et al.
Publicado: (2022) -
Ocular Tonometry and Sporadic Creutzfeldt - Jakob Disease (sCJD): A Confirmatory Case-Control Study
por: Davanipour, Zoreh, et al.
Publicado: (2014) -
Profile Of Patients With Advanced Parkinson’s disease Suitable For Device-Aided Therapies: Restrospective Data Of A Large Cohort Of Romanian Patients
por: Szász, József Attila, et al.
Publicado: (2019) -
Neuropathological changes in striate and extrastriate visual cortex in variant Creutzfeldt-Jakob disease (vCJD)
por: Armstrong, Richard A
Publicado: (2007) -
A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom
por: Nagata, Tomoyuki, et al.
Publicado: (2021)