Creutzfeldt-Jakob Disease – A Series of Four Clinical Cases
Creutzfeldt-Jakob Disease (CJD) is a rare, progressive, and fatal degenerative brain disorder caused by prion proteins. The diagnosis of the disease is based on established criteria and biomarkers – cerebrospinal fluid analysis, real-time quaking induced conversion (RT-QulC), magnetic resonance imag...
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| Asıl Yazarlar: | , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Sciendo
2025-09-01
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| Seri Bilgileri: | Acta Medica Bulgarica |
| Konular: | |
| Online Erişim: | https://doi.org/10.2478/amb-2025-00064 |
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