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Eva Parobková

Observed names: E. Parobkova, E. Parobková, Eva Parobkova, Parobková, Eva
OpenAlex ID: A5001204350
A Pan‐ E uropean Study of the C9orf72 Repeat Associated with FTLD : Geographic Prevalence, Genomic Instability, and Intermediate Repeats
2012 · Julie van der Zee, Ilse Gijselinck, et al. · Human Mutation · 277
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
2014 · Julie van der Zee, Tim Van Langenhove, et al. · Acta Neuropathologica · 121
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Clinical Variability in P102L Gerstmann–Sträussler–Scheinker Syndrome
2019 · Adam Tesar, Radoslav Matej, et al. · Annals of Neurology · 41
Real-world EGFR testing practices for non-small-cell lung cancer by thoracic pathology laboratories across Europe
2023 · P. Hofman, F. Calabrese, et al. · ESMO Open · 33
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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
2018 · Yalda Baradaran-Heravi, Lubina Dillen, et al. · Neurobiology of Aging · 29
Human Prion Disorders: Review of the Current Literature and a Twenty-Year Experience of the National Surveillance Center in the Czech Republic
2021 · Nikol Jankovska, Robert Rusina, et al. · Diagnostics · 25
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Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degenerations: Similarities in Genetic Background
2021 · Eva Parobkova, Radoslav Matej · Diagnostics · 25
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Biomarkers Analysis and Clinical Manifestations in Comorbid Creutzfeldt–Jakob Disease: A Retrospective Study in 215 Autopsy Cases
2022 · Nikol Jankovska, Robert Rusina, et al. · Biomedicines · 9
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Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity
2020 · Eva Parobkova, Julie van der Zee, et al. · Frontiers in Neurology · 8
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PART and ARTAG tauopathies at a relatively young age as a concomitant finding in sporadic Creutzfeldt-Jakob disease
2021 · Kateřina Menšíková, Radoslav Matěj, et al. · Prion · 6
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Genetics of neurodegenerative dementias in ten points – what can a neurologist expect from molecular genetics?
2019 · Eva Parobková, Robert Rusina, et al. · Česká a slovenská neurologie a neurochirurgie · 3
Parallel Liquid Biopsy Analysis of miR‐371a‐3p and Cell‐Free DNA in an Unselected Cohort of Patients With Testicular Germ Cell Tumors
2026 · Laura Matouskova, Romy Kralova, et al. · Andrology · 1
Detection of EGFR Mutations in Circulating Tumor DNA (ctDNA) Retrieved from Plasma – Interlaboratory Quality Assessment in the Czech Republic
2018 · Linda Čapková, Markéta Kalinová, et al. · Klinicka onkologie · 1
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Homozygous RSPO1–NUMT insertion is associated with earlier onset of lung adenocarcinoma (LUAD)
2026 · Ilona Tietzova, Dana Sochorova, et al. · European Respiratory Journal
Yield of genetic testing and telomere length assessment in czech patients with interstitial lung disease
2026 · Martina Šterclová, Andrea Holubova, et al. · European Respiratory Journal
Gerstmann-Sträussler-Scheinker syndrome with unexpected concomitant GRN variant: case report
2026 · Matyas Sykora, Bibiana Krenkova, et al. · Frontiers in Neuroscience
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Parallel liquid biopsy analysis of miR-371a-3p and cell-free DNA in testicular germ cell tumors.
2026 · Laura Matouskova, Romy Kralova, et al. · Journal of Clinical Oncology
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An unexpected discovery of a novel potentially pathogenic APP gene variant: a case report of slowly progressive Alzheimer’s disease with prominent cerebral amyloid angiopathy
2026 · Matyas Sykora, Marie Harmackova, et al. · Frontiers in Neuroscience
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Gerstmann–Sträussler–Scheinker syndrome neuropathology in a Creutzfeldt–Jakob disease-like phenotype patient caused by a novel 6-OPRI sequence in the PRNP gene
2025 · M. Sýkora, S. Baranová, et al. · Revue Neurologique
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
2025 · Ilona Tietzova, Dana Sochorova, et al. · Translational Lung Cancer Research
Even extraordinary things could be ordinary: a case report of atypical neurodegeneration due to vascular and malnutrition components
2025 · Matyáš Sýkora, Eva Parobková, et al. · Neurologie pro praxi
Analysis of associated genes with neurodegenerative diseases: practical experience of neurodegenerative centers in FTN
2024 · Eva Parobková, Petr Šuhaj, et al. · Neurologie pro praxi
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Molecular genetic aspects of neurodegenerative diseases
2021 · Parobková, Eva · Digital Repository (National Repository of Grey Literature)
Genetika neurodegenerativních demencí v deseti bodech: co může neurolog očekávat od molekulárního genetika?
2019 · Eva Parobková
Human prion diseases.
2008 · Parobková, Eva · Digital Repository (National Repository of Grey Literature)
Works count: 26
Citation count: 856
H-index: 9
I10-index: 8
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