Publications by authors named "Eva Parobkova"

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Identification of a novel RSPO1-NUMT insertion in a LUAD patient cohort and the challenges and insights into NUMT detection highlighting the importance of reference genomes and population databases.
Ilona Tietzova, Dana Sochorova, Petr Triska, Rebecca C Rancourt, Marek Omelka, Eva Parobkova

Transl Lung Cancer Res· October 2025

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Biomarkers Analysis and Clinical Manifestations in Comorbid Creutzfeldt-Jakob Disease: A Retrospective Study in 215 Autopsy Cases.
Nikol Jankovska, Robert Rusina, Jiri Keller, Jaromir Kukal, Magdalena Bruzova, Eva Parobkova

Biomedicines· March 2022

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PART and ARTAG tauopathies at a relatively young age as a concomitant finding in sporadic Creutzfeldt-Jakob disease.
Kateřina Menšíková, Radoslav Matěj, Eva Parobková, Magdalena Smětáková, Petr Kaňovský

Prion· December 2021

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Human Prion Disorders: Review of the Current Literature and a Twenty-Year Experience of the National Surveillance Center in the Czech Republic.
Nikol Jankovska, Robert Rusina, Magdalena Bruzova, Eva Parobkova, Tomas Olejar

Diagnostics (Basel)· October 2021

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Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degenerations: Similarities in Genetic Background.
Eva Parobkova, Radoslav Matej

Diagnostics (Basel)· March 2021

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Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity.
Eva Parobkova, Julie van der Zee, Lubina Dillen, Christine Van Broeckhoven, Robert Rusina

Front Neurol· November 2020

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Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome.
Adam Tesar, Radoslav Matej, Jaromir Kukal, Silvie Johanidesova, Irena Rektorova, Eva Parobkova

Ann Neurol· November 2019

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Detection of EGFR Mutations in Circulating Tumor DNA (ctDNA) Retrieved from Plasma - Interlaboratory Quality Assessment in the Czech Republic.
Čapková Linda, Kalinová Markéta, Tichá Ivana, Parobková Eva, Matějčková Milada

Klin Onkol· August 2019

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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients.
Yalda Baradaran-Heravi, Lubina Dillen, Hung Phuoc Nguyen, Sara Van Mossevelde, Jonathan Baets, Eva Parobkova

Neurobiol Aging· September 2018

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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.
Julie van der Zee, Tim Van Langenhove, Gabor G Kovacs, Lubina Dillen, William Deschamps, Eva Parobkova

Acta Neuropathol· September 2014

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A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.
Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Eva Parobkova, Eva Parobkova

Hum Mutat· February 2013

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