17 results on '"Matěj, Radoslav"'
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2. High tumour mutational burden is associated with strong PD-L1 expression, HPV negativity, and worse survival in penile squamous cell carcinoma: an analysis of 165 cases
3. Microsatellite instability in non-endometrioid ovarian epithelial tumors: a study of 400 cases comparing immunohistochemistry, PCR, and NGS based testing with mutation status of MMR genes
4. Refined criteria for p53 expression in ovarian mucinous tumours are highly concordant with TP53 mutation status, but p53 expression/TP53 status lack prognostic significance
5. Pathologic Criteria for the Diagnosis of Usual Interstitial Pneumonia vs Fibrotic Hypersensitivity Pneumonitis in Transbronchial Cryobiopsies
6. Immune cell infiltration, tumour budding, and the p53 expression pattern are important predictors in penile squamous cell carcinoma: a retrospective study of 152 cases
7. Alzheimer ’s disease identification from 3D SPECT brain scans by variational analysis
8. Primary Mucinous Tumors of the Ovary: An Interobserver Reproducibility and Detailed Molecular Study Reveals Significant Overlap Between Diagnostic Categories
9. Bilateral thalamic glioblastoma presenting as parkinsonism: A case report
10. Alzheimer's disease and other neurodegenerative dementias in comorbidity: A clinical and neuropathological overview
11. Choriogonadotropin positive seminoma—a clinicopathological and molecular genetic study of 15 cases
12. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
13. Increased neuronal Rab5 immunoreactive endosomes do not colocalize with TDP-43 in motor neuron disease
14. Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study
15. Lung Cancer in the Czech Republic
16. NEUTROPHIL EXTRACELLULAR TRAPS (NETS) AND THROMBOLYSIS RESISTANCE - COMPARATIVE ANALYSIS OF THROMBOTIC/EMBOLIC SPECIMENS, RETRIEVED FROM CEREBRAL ARTERIES AFTER MECHANICAL THROMBECTOMY AND CORONARY ARTERY THROMBUS ASPIRATION IN MYOCARDIAL INFARCTION
17. No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
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