Pawel P Liberski
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Explore the profile of Pawel P Liberski including associated specialties, affiliations and a list of published articles.
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155
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9127
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Recent Articles
1.
Kucukali F, Hill E, Watzeels T, Hummerich H, Campbell T, Darwent L, et al.
Brain
. 2025 Jan;
PMID: 39865733
Prions are assemblies of misfolded prion protein that cause several fatal and transmissible neurodegenerative diseases, with the most common phenotype in humans being sporadic Creutzfeldt-Jakob disease (sCJD). Aside from variation...
2.
Hummerich H, Speedy H, Campbell T, Darwent L, Hill E, Collins S, et al.
PLoS One
. 2024 Jul;
19(7):e0304528.
PMID: 39079175
Human prion diseases are rare, transmissible and often rapidly progressive dementias. The most common type, sporadic Creutzfeldt-Jakob disease (sCJD), is highly variable in clinical duration and age at onset. Genetic...
3.
Dulski J, Koga S, Liberski P, Sitek E, Butala A, Slawek J, et al.
Mov Disord Clin Pract
. 2023 Jul;
10(7):1136-1142.
PMID: 37476320
Background: Perry disease (or Perry syndrome [PS]) is a hereditary neurodegenerative disorder inevitably leading to death within few years from onset. All previous cases with pathological confirmation were caused by...
4.
Kikuchi F, Arai S, Hejduk J, Hayashi A, Markowski J, Markowski M, et al.
Viruses
. 2023 Apr;
15(4).
PMID: 37112861
Earlier, we demonstrated the co-circulation of genetically distinct non-rodent-borne hantaviruses, including Boginia virus (BOGV) in the Eurasian water shrew (), Seewis virus (SWSV) in the Eurasian common shrew () and...
5.
Szmyd B, Solek J, Blaszczyk M, Jankowski J, Liberski P, Jaskolski D, et al.
Front Mol Neurosci
. 2022 Jul;
15:923089.
PMID: 35860499
Neurovascular compression syndromes (NVC) are challenging disorders resulting from the compression of cranial nerves at the root entry/exit zone. Clinically, we can distinguish the following NVC conditions: trigeminal neuralgia, hemifacial...
6.
Schmitz M, Villar-Pique A, Hermann P, Escaramis G, Calero M, Chen C, et al.
Brain
. 2022 Mar;
145(2):700-712.
PMID: 35288744
Genetic prion diseases are a rare and diverse group of fatal neurodegenerative disorders caused by pathogenic sequence variations in the prion protein gene, PRNP. Data on CSF biomarkers in patients...
7.
Witusik-Perkowska M, Jaskolski D, Liberski P, Szemraj J
Cell Mol Neurobiol
. 2020 Nov;
42(4):1005-1020.
PMID: 33245508
The tumor resistance of glioblastoma cells in vivo is thought to be enhanced by their heterogeneity and plasticity, which are extremely difficult to curb in vitro. The external microenvironment shapes...
8.
Jones E, Hummerich H, Vire E, Uphill J, Dimitriadis A, Speedy H, et al.
Lancet Neurol
. 2020 Sep;
19(10):840-848.
PMID: 32949544
Background: Human prion diseases are rare and usually rapidly fatal neurodegenerative disorders, the most common being sporadic Creutzfeldt-Jakob disease (sCJD). Variants in the PRNP gene that encodes prion protein are...
9.
Gruszka R, Zakrzewski K, Liberski P, Zakrzewska M
Folia Neuropathol
. 2020 Jul;
58(2):123-132.
PMID: 32729291
Nowadays molecular investigations have a significant impact on the understanding of primary brain tumour biology,as well as on their classification and progress in the treatment modalities. Among novel type of...
10.
Witusik-Perkowska M, Zakrzewska M, Jaskolski D, Liberski P, Szemraj J
Onco Targets Ther
. 2019 Jun;
12:3905-3918.
PMID: 31190889
The in vitro environment can influence not only the molecular background of glioblastoma drug-resistance and treatment efficiency, but also the mechanisms and pathways of cell death. Both crucial molecular pathways...