Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Eva Parobková"'
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:
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
Autor:
Eva Parobkova, Radoslav Matej
Publikováno v:
Diagnostics, Vol 11, Iss 3, p 509 (2021)
Amyotrophic lateral sclerosis (ALS) is a devastating, uniformly lethal progressive degenerative disorder of motor neurons that overlaps with frontotemporal lobar degeneration (FTLD) clinically, morphologically, and genetically. Although many distinct
Externí odkaz:
https://doaj.org/article/1ad9cce68a4d4469a3619ec930a7e117
Autor:
Linda Čapková, Markéta Kalinová, Ivana Tichá, Eva Parobková, Milada Matějčková, Hana Vošmiková, Ondřej Horký, Karolína Bartáková, Jiří Drábek, Monika Bajerová, Pavel Dundr
Publikováno v:
Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti. 31(5)
Detection of EGFR mutations in tumor tissue represents a standard testing procedure in patients with non-small cell lung cancer. Molecular testing of circulating tumor DNA (ctDNA) in plasma enables detection of mutations in cases where tumor specimen
Autor:
Linda, Čapková, Markéta, Kalinová, Ivana, Tichá, Eva, Parobková, Milada, Matějčková, Hana, Vošmiková, Ondřej, Horký, Karolína, Bartáková, Jiří, Drábek, Monika, Bajerová, Pavel, Dundr
Publikováno v:
Journal of the Czech & Slovak Societies for Oncology / Klinická Onkologie; 2018, Vol. 31 Issue 5, p353-360, 8p
Autor:
Eva Parobkova, Julie van der Zee, Lubina Dillen, Christine Van Broeckhoven, Robert Rusina, Radoslav Matej
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Sporadic Creutzfeldt–Jakob disease (sCJD) is the most common type of a group of transmissible spongiform encephalopathies (prion diseases). The etiology of the sporadic form of CJD is still unclear. sCJD can occur in combination with ot
Externí odkaz:
https://doaj.org/article/b4da639e49a44ee7af41495611c96585