591 results on '"Miele, Evelina"'
Search Results
2. The coexistence of a BRCA2 germline and a DICER1 somatic variant in two first-degree cousins suggests their potential synergic effect
3. Evaluating cell culture reliability in pediatric brain tumor primary cells through DNA methylation profiling
4. CNS tumor with CREBBP::BCORL1 Fusion and pathogenic mutations in BCOR and CREBBP: expanding the spectrum of BCOR-altered tumors
5. Malignant peripheral nerve sheath tumor (MPNST) and MPNST-like entities are defined by a specific DNA methylation profile in pediatric and juvenile population
6. Spindle Cell Lesions with Oncogenic EGFR Kinase Domain Aberrations: Expanding the Spectrum of Protein Kinase–Related Mesenchymal Tumors
7. Intracranial mesenchymal tumor with (novel) COX14::PTEN rearrangement
8. Exceptionally rare IDH1-mutant adult medulloblastoma with concurrent GNAS mutation revealed by in vivo magnetic resonance spectroscopy and deep sequencing
9. Optimizing reirradiation for relapsed medulloblastoma: identifying the ideal patient and tumor profiles
10. Case report of a pediatric medulloblastoma with concurrent MYC and MYCN subclonal amplification in distinct populations of neoplastic cells
11. Clinicopathological and molecular landscape of 5-year IDH-wild-type glioblastoma survivors: A multicentric retrospective study
12. PATZ1-Rearranged Tumors of the Central Nervous System: Characterization of a Pediatric Series of Seven Cases
13. Identification of a robust DNA methylation signature for Fanconi anemia
14. Coexistence of a BRCA2 germline and a DICER1 somatic variant in two first- degree young cousins: a potential cooperative role in determining cancer susceptibility?
15. Growing teratoma syndrome in children and adolescents: Prevalence and surgical outcome
16. Gliomatosis cerebri in children: A poor prognostic phenotype of diffuse gliomas with a distinct molecular profile
17. MiR-1248: a new prognostic biomarker able to identify supratentorial hemispheric pediatric low-grade gliomas patients associated with progression
18. A slow-cycling/quiescent cells subpopulation is involved in glioma invasiveness
19. A case of glioneuronal tumour with ATRX alteration, kinase fusion and anaplastic features showing rapid ependymal and leptomeningeal dissemination.
20. GOPC:ROS1 and other ROS1 fusions represent a rare but recurrent drug target in a variety of glioma types
21. PATZ1 fusions define a novel molecularly distinct neuroepithelial tumor entity with a broad histological spectrum
22. A supratentorial mass in a young adult, with 25 years of follow‐up
23. Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists?
24. Targeting cancer stem cells in medulloblastoma by inhibiting AMBRA1 dual function in autophagy and STAT3 signalling
25. Pediatric low-grade gliomas: molecular characterization of patient-derived cellular models
26. Machine Learning Analysis in Diffusion Kurtosis Imaging for Discriminating Pediatric Posterior Fossa Tumors: A Repeatability and Accuracy Pilot Study.
27. Role of 18F-Fluorodeoxyglucose Positron Emission Tomography in Children With Germ Cell Tumor After Chemotherapy.
28. Case report of a pediatric medulloblastoma with concurrent MYC and MYCN subclonal amplification in distinct populations of neoplastic cells.
29. Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists?
30. PATZ1-rearranged tumors of the central nervous system: characterization of a pediatric series of seven cases
31. Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile
32. Cytotoxic effects and tolerability of gemcitabine and axitinib in a xenograft model for c-myc amplified medulloblastoma
33. Central nervous system high-grade neuroepithelial tumor with BCOR alteration (CNS HGNET-BCOR)—case-based reviews
34. Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging
35. Mesenchymal PLAG1 Tumor With PCMTD1-PLAG1 Fusion in an Infant: A New Type of “Plagoma”
36. Role of 18F-Fluorodeoxyglucose Positron Emission Tomography in Children With Germ Cell Tumor After Chemotherapy
37. Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation
38. High-Grade Gliomas and Cancer Predisposition Syndromes in children and adolescents: Unpacking the Impact through a Single-Center Analysis
39. Oncology: Solid Mass in Pediatrics and Malignant Bone Involvement
40. Oncology
41. Cerebellar mass in a 31‐year‐old woman.
42. Modeling medulloblastoma in vivo and with human cerebellar organoids
43. Intrathoracic synovial sarcoma with BRAF V600E mutation
44. HGG-17. SINGLE-CELL AND SPATIAL ANALYSES DECIPHER THE UNIQUE INVASIVE GROWTH PATTERN OF GLIOMATOSIS CEREBRI
45. Medulloblastoma at relapse: for which patients and which tumors reirradiation is the better choice
46. Robot-Assisted Stereotactic Biopsy of Diffuse Intrinsic Pontine Glioma: A Single-Center Experience
47. BRAF mutant colorectal cancer: ErbB2 expression levels as predictive factor for the response to combined BRAF/ErbB inhibitors
48. Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature
49. KCTD15 inhibits the Hedgehog pathway in Medulloblastoma cells by increasing protein levels of the oncosuppressor KCASH2
50. Patient‐ and xenograft‐derived organoids recapitulate pediatric brain tumor features and patient treatments.
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