S Bräuer, V Zimyanin, A Hermann - Journal of Neural Transmission, 2018 - Springer
The hallmark of age-related neurodegenerative diseases is the appearance of cellular protein deposits and spreading of this pathology throughout the central nervous system …
F Ghodrati, M Mehrabian, D Williams, O Halgas… - Scientific Reports, 2018 - nature.com
At times, it can be difficult to discern if a lack of overlap in reported interactions for a protein- of-interest reflects differences in methodology or biology. In such instances, systematic …
Abstract Background Creutzfeldt–Jakob disease is a rare and rapidly fatal neurodegenerative disease. Since clinicians may see only very few cases during their …
A Milovidov, T Matsalu, M Kaarlõp, T Toomsoo - Eesti Arst, 2018 - ojs.utlib.ee
Prioonhaigused on haruldased neurodegeneratiivsed haigused, mis põhjustavad kiire kuluga dementsuse ja lõpevad alati surmaga. Creutzfeldti-Jakobi tõbi kuulub prioonhaiguste …
The pathogenic mechanisms and the origins of neurodegenerative diseases remain unclear on molecular level. Increasing evidences postulate alterations in miRNA signatures as …
Las enfermedades priónicas, también conocidas como encefalopatías espongiformes transmisibles (EETs), son enfermedades neurodegenerativas que afectan a humanos y …
Ó López-Pérez, R Bolea Bailo, I Martín Burriel - 2018 - zaguan.unizar.es
Las encefalopatías espongiformes transmisibles (EETs), o enfermedades priónicas, son un grupo de trastornos neurodegenerativos fatales que afectan a los animales y al hombre …
Transmissible spongiform encephalopathies (TSEs) or prion diseases, are subacute neurodegenerative diseases that infect humans and animals. Many of these diseases are …