Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Adam Tesar"'
Autor:
Petra Nytrova, Dominika Stastna, Adam Tesar, Ingrid Menkyova, Helena Posova, Helena Koprivova, Veronika Mikulova, Jiri Hrdy, Gabriela Smela, Dana Horakova, Irena Rysankova, Kristyna Doleckova, Michaela Tyblova
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundRituximab (RTX) and ocrelizumab (OCR), B cell-depleting therapy targeting CD20 molecules, affect the humoral immune response after vaccination. How these therapies influence T-cell-mediated immune response against SARS-CoV-2 after immunizat
Externí odkaz:
https://doaj.org/article/fd83e3caa4d14846b4d386ffddd286ce
Autor:
Zuzana Stejskalova, Zdenek Rohan, Robert Rusina, Adam Tesar, Jaromir Kukal, Gabor G. Kovacs, Ales Bartos, Radoslav Matej
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background We aimed to produce a detailed neuropathological analysis of pyramidal motor system pathology and provide its clinical pathological correlation in cases with definite progressive supranuclear palsy (PSP). Methods Pyramidal motor s
Externí odkaz:
https://doaj.org/article/7f24de3257b740e4b8007af784178d02
Autor:
Adam Tesar, Zdenek Rohan, Radoslav Matej, Zuzana Stejskalova, Robert Rusina, Jaromir Kukal, Ales Bartos, Gabor G. Kovacs
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-8 (2019)
BMC Neurology
BMC Neurology
Background We aimed to produce a detailed neuropathological analysis of pyramidal motor system pathology and provide its clinical pathological correlation in cases with definite progressive supranuclear palsy (PSP). Methods Pyramidal motor system pat
Publikováno v:
Clinical biochemistry. 73
Neuropathological diagnostic criteria of neurodegenerative disorders are based on the presence of specific inclusions in a specific area of brain tissue that correlate with clinical manifestations. Concomitant neurodegenerative disorders correspond t
Autor:
Irena Rektorová, Eva Parobkova, Zuzana Musova, Adam Tesar, Radoslav Matej, Silvie Johanidesova, Jaromir Kukal, Robert Rusina, Martin Vyhnalek, Magdalena Smetakova, Ilona Eliasova, Jiri Keller
Publikováno v:
Annals of neurologyReferences. 86(5)
Gerstmann-Straussler-Scheinker syndrome (GSS) with the P102L mutation is a rare genetic prion disease caused by a pathogenic mutation at codon 102 in the prion protein gene. Cluster analysis encompassing data from 7 Czech patients and 87 published ca