Zobrazeno 1 - 3
of 3
pro vyhledávání: '"physiopathology [Gliosis]"'
Autor:
Sergey Ryazanov, Song Shi, Hans A. Kretzschmar, Wolfgang Zinth, Andrei Leonov, Martin Fuhrmann, Carolin Miklitz, Armin Giese, Daniel Weckbecker, Dan Ehninger, Bettina Göricke, Anne Reiner, Julia Steffen, Jens Wagner, Jochen H. Weishaupt, Alexander Kleinknecht, Johannes Levin, Stefan Remy, Christian Griesinger, Sybille Krauss
Publikováno v:
Acta Neuropathologica
Acta neuropathologica 130(5), 619-631 (2015). doi:10.1007/s00401-015-1483-3
Acta neuropathologica 130(5), 619-631 (2015). doi:10.1007/s00401-015-1483-3
Pathological tau aggregation leads to filamentous tau inclusions and characterizes neurodegenerative tauopathies such as Alzheimer’s disease and frontotemporal dementia and parkinsonism linked to chromosome 17. Tau aggregation coincides with clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5d7327b3d660fae3c7d3a6ab97d5440
http://europepmc.org/articles/PMC4612332
http://europepmc.org/articles/PMC4612332
Autor:
Christoph Harms, Nafisa M. Jadavji, Marco Foddis, Ulrich Dirnagl, Janet Lips, Philipp Boehm-Sturm, Ahmed A. Khalil, Martina Füchtemeier, Tracy D. Farr
Publikováno v:
Behavioural brain research 283, 215-226 (2015). doi:10.1016/j.bbr.2015.01.040
Dietary deficiencies in folic acid result in elevated levels of plasma homocysteine, which has been associated with the development of dementia and other neurodegenerative disorders. Previously, we have shown that elevated levels of plasma homocystei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a53da5e5acbfbaaf8120dbd2ad3a7c5
https://doi.org/10.1016/j.bbr.2015.01.040
https://doi.org/10.1016/j.bbr.2015.01.040
Autor:
Franc Llorens, Juan J. Zarranz, Margalida A. Frau-Méndez, Isidro Ferrer, Iván Fernández-Vega, Katrin Thüne, Inga Zerr, Nadine Gotzmann, Christopher J. Silva, Belén Ansoleaga, Matthias Schmitz, Maria Cramm, Margarita Carmona, Waqas Tahir, Sara Berjaoui
Publikováno v:
Human molecular genetics 25(12), ddw108 (2016). doi:10.1093/hmg/ddw108
Europe PubMed Central
Scopus-Elsevier
Europe PubMed Central
Scopus-Elsevier
Fatal familial insomnia is a rare disease caused by a D178N mutation in combination with methionine (Met) at codon 129 in the mutated allele of PRNP (D178N-129M haplotype). FFI is manifested by sleep disturbances with insomnia, autonomic disorders an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d1b6be2c33573d45377a546579e5810
https://pub.dzne.de/record/139013
https://pub.dzne.de/record/139013
