Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Magdalena Brůžová"'
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Various proteins play a decisive role in the pathology of different neurodegenerative diseases. Nonetheless, most of these proteins can only be detected during a neuropathological assessment, although some non-specific biomarkers are routine
Externí odkaz:
https://doaj.org/article/de857d9a05f547e2872766e12499d608
Autor:
Nikol Jankovska, Robert Rusina, Jiri Keller, Jaromir Kukal, Magdalena Bruzova, Eva Parobkova, Tomas Olejar, Radoslav Matej
Publikováno v:
Biomedicines, Vol 10, Iss 3, p 680 (2022)
Creutzfeldt–Jakob disease (CJD), the most common human prion disorder, may occur as “pure” neurodegeneration with isolated prion deposits in the brain tissue; however, comorbid cases with different concomitant neurodegenerative diseases have be
Externí odkaz:
https://doaj.org/article/12872e8d15424f4893994aa58940fd61
Autor:
Soňa Baranová, Tibor Moško, Magdalena Brůžová, Tracy Haldiman, Chae Kim, Jiri G. Safar, Radoslav Matěj, Karel Holada
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Real-time quaking-induced conversion assay (RT-QuIC) exploits templating activity of pathogenic prion protein for ultrasensitive detection of prions. We have utilized second generation RT-QuIC assay to analyze matching post-mortem cerebrospi
Externí odkaz:
https://doaj.org/article/4a0a7a4517b84d01adcc462d7d759046
Publikováno v:
Pathogens, Vol 10, Iss 6, p 750 (2021)
The possibilities for diagnosing prion diseases have shifted significantly over the last 10 years. The RT-QuIC assay option has been added for neuropsychiatric symptoms, supporting biomarkers and final post-mortem confirmation. Samples of brain homog
Externí odkaz:
https://doaj.org/article/862522c0c3f944ff90aa53b2b9b4cccc
Publikováno v:
Česká a slovenská neurologie a neurochirurgie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3d3da24939fe502613670953b41c3e0
https://doi.org/10.48095/cccsnn2022511
https://doi.org/10.48095/cccsnn2022511
Publikováno v:
Pathogens; Volume 10; Issue 6; Pages: 750
The possibilities for diagnosing prion diseases have shifted significantly over the last 10 years. The RT-QuIC assay option has been added for neuropsychiatric symptoms, supporting biomarkers and final post-mortem confirmation. Samples of brain homog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::ae7f78ff7c319acc629464baadac34d9
Autor:
Marie Drosslerova, Martina Sterclova, Alice Taskova, Vladislav Hytych, Eva Richterova, Magdalena Bruzova, Miloslav Spunda, Martin Komarc, Martina Koziar Vasakova
Publikováno v:
Biomedical Papers, Vol 167, Iss 4, Pp 335-339 (2023)
Background. Complex networks of chemokines are part of the immune reaction targeted against tumor cells. Chemokines influence cancer growth. It is unclear whether the concentrations of chemokines at the time of NSCLC (non-small cell lung cancer) diag
Externí odkaz:
https://doaj.org/article/cdb042e436c5401883928ef204a844be
Autor:
Martina Sterclova, Veronika Kremlackova, Veronika Mottlova, Magdalena Bruzova, Pavel Sojka, Martina Vasakova
Publikováno v:
Cogent Medicine, Vol 8, Iss 1 (2021)
Abstract: Assessment of humoral response to inhalation antigens is currently the most frequently used method to confirm exposure. It may be useful in extrinsic allergic alveolitis (EAA) patients, especially in cases that are unaware of the source of
Externí odkaz:
https://doaj.org/article/b4a654353bc741b7be6cb2fc5d180bc5
Autor:
Nikol Jankovska, Robert Rusina, Magdalena Bruzova, Eva Parobkova, Tomas Olejar, Radoslav Matej
Publikováno v:
Diagnostics, Vol 11, Iss 10, p 1821 (2021)
Human prion disorders (transmissible spongiform encephalopathies, TSEs) are unique, progressive, and fatal neurodegenerative diseases caused by aggregation of misfolded prion protein in neuronal tissue. Due to the potential transmission, human TSEs a
Externí odkaz:
https://doaj.org/article/760cf9e50f9e4926824bcfb6b79e2ff8
Publikováno v:
Diagnostics, Vol 11, Iss 4, p 693 (2021)
Idiopathic interstitial pneumonia (IIP) entails a variable group of lung diseases of unknown etiology. Idiopathic pulmonary fibrosis, nonspecific interstitial pneumonia, interstitial lung diseases related to connective tissue disease (CTD-ILD), and h
Externí odkaz:
https://doaj.org/article/983b3b2376d5418ead04d0a12dd3a6d9