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Your search keyword '"Palova, Hana"' showing total 21 results

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21 results on '"Palova, Hana"'

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1. Diagnostic efficacy and clinical utility of whole-exome sequencing in Czech pediatric patients with rare and undiagnosed diseases

2. Precision immuno-oncology approach for four malignant tumors in siblings with constitutional mismatch repair deficiency syndrome

3. Real-World Performance of Integrative Clinical Genomics in Pediatric Precision Oncology

6. The landscape of tumor cell states and spatial organization in H3-K27M mutant diffuse midline glioma across age and location

7. Personalized dendritic cell vaccine in multimodal individualized combination therapy improves survival in high‐risk pediatric cancer patients.

9. Diagnostic yield and clinical utility of whole-exome sequencing in pediatric patients with rare and undiagnosed diseases: a prospective, single-center study from the Czech Republic

10. Minimal Residual Disease–Guided Intermittent Dosing in Patients With Cancer: Successful Treatment of Chemoresistant Anaplastic Large Cell Lymphoma Using Intermittent Lorlatinib Dosing

11. DDDR-17. CLINICAL RESPONSE TO THE PDGFRA/KIT INHIBITOR AVAPRITINIB IN PEDIATRIC AND YOUNG ADULT HIGH-GRADE GLIOMA PATIENTS

12. Abstract 1063: Precision medicine and cancer drug repurposing in the management of vascular anomalies

13. Abstract 4511: Impact of the comprehensive genomic profiling on the individual therapeutic planning in high-risk/refractory tumors: real-world precision medicine in pediatric oncology

15. EPCO-21. THE SPATIAL ORGANIZATION OF H3-K27M MUTANT DIFFUSE MIDLINE GLIOMA

16. DDDR-22. TRANSLATION OF THE PDGFRA/KIT INHIBITOR AVAPRITINIB FOR PEDIATRIC HIGH-GRADE GLIOMA

17. Risk factors for tumors or leukemia development in the first two years of life.

18. Abstract 76: Comprehensive genomic profiling as an approach to guide therapeutic planning in pediatric patients with high-risk solid tumors

19. DIPG-60. Avapritinib for targeting PDGFRA in H3K27M – mutated diffuse midline glioma

21. Spindle Cell Hemangioma and Atypically Localized Juxtaglomerular Cell Tumor in a Patient with Hereditary BRIP1 Mutation: A Case Report

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