186 results on '"Métais, Alice"'
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2. Diffuse pediatric high-grade glioma of methylation-based RTK2A and RTK2B subclasses present distinct radiological and histomolecular features including Gliomatosis cerebri phenotype
3. Diffuse glioneuronal tumor with oligodendroglioma-like features and nuclear clusters (DGONC), new name and new problems: an illustration of one case with atypical morphology and biology
4. Atrx loss as a promising screening tool for the identification of diffuse midline glioma subtype, H3K27/MAPKinase co-altered
5. CNS tumors with PLAGL1-fusion: beyond ZFTA and YAP1 in the genetic spectrum of supratentorial ependymomas
6. CNS erythroblastic sarcoma: a potential emerging pediatric tumor type characterized by NFIA::RUNX1T1/3 fusions
7. PLAG1 fusions extend the spectrum of PLAG(L)-altered CNS tumors
8. Refinement of diagnostic criteria for pediatric-type diffuse high-grade glioma, IDH- and H3-wildtype, MYCN-subtype including histopathology, TP53, MYCN and ID2 status
9. Diagnostic accuracy of a minimal immunohistochemical panel in at/rt molecular subtyping, correlated to dna-methylation profiling
10. CNS neuroblastoma, FOXR2-activated and its mimics: a relevant panel approach for work-up and accurate diagnosis of this rare neoplasm
11. A sellar presentation of a WNT-activated embryonal tumor: further evidence of an ectopic medulloblastoma
12. CNS tumor with EP300::BCOR fusion: discussing its prevalence in adult population
13. Pediatric-type high-grade neuroepithelial tumors with CIC gene fusion share a common DNA methylation signature
14. Clinico-pathological and epigenetic heterogeneity of diffuse gliomas with FGFR3::TACC3 fusion
15. NF2 and ZFTA evaluation in the diagnostic algorithm of pediatric posterior fossa ependymoma with H3K27ME3 retained expression
16. Mesenchymal non-meningothelial tumors of the central nervous system: a literature review and diagnostic update of novelties and emerging entities
17. Apports et limites de la FISH dans le diagnostic des tumeurs du système nerveux central selon la classification de l’OMS de 2021 : retour d’expérience du service de neuropathologie de l’hôpital Sainte-Anne
18. Pediatric spinal pilocytic astrocytomas form a distinct epigenetic subclass from pilocytic astrocytomas of other locations and diffuse leptomeningeal glioneuronal tumours
19. An extracranial CNS presentation of the emerging “intracranial” mesenchymal tumor, FET: CREB-fusion positive
20. Clinicopathological and molecular characterization of three cases classified by DNA-methylation profiling as “Glioneuronal Tumors, NOS, Subtype A”
21. Ré-utilisation de lames d’immunohistochimie pour la réalisation de FISH : une solution pertinente d’épargne tissulaire
22. Pediatric high-grade gliomas with concomitant RB1 and SETD2 alterations and Li-Fraumeni syndrome.
23. Phenotypic and epigenetic heterogeneity in FGFR2‐fused glial and glioneuronal tumours.
24. A comprehensive histomolecular characterization of meningioangiomatosis: Further evidence for a precursor neoplastic lesion.
25. A novel YAP1-MAML2 fusion in an adult supra-tentorial ependymoma, YAP1-fused
26. A novel LARGE1-AFF2 fusion expanding the molecular alterations associated with the methylation class of neuroepithelial tumors with PATZ1 fusions
27. The dural angioleiomyoma harbors frequent GJA4 mutation and a distinct DNA methylation profile
28. Posterior fossa ependymoma H3 K27-mutant: an integrated radiological and histomolecular tumor analysis
29. Disseminated diffuse midline gliomas, H3K27-altered mimicking diffuse leptomeningeal glioneuronal tumors: a diagnostical challenge!
30. Immunohistochemistry as a tool to identify ELP1-associated medulloblastoma
31. Le diagnostic histo-moléculaire des tumeurs gliales et glioneuronales
32. A non-midline unclassified glioneuronal tumor with H3K27M mutation enlarging the spectrum of CNS tumors H3K27ME3-altered.
33. Utility of combining OLIG2 and SOX10 IHC expression in CNS tumours: promising biomarkers for subtyping paediatric‐ and adult‐type gliomas
34. LEF-1 immunohistochemistry, a better diagnostic biomarker than β-catenin for medulloblastoma, WNT-activated subtyping
35. “Hemispheric pilocytic astrocytoma” revisited: A comprehensive clinicopathological and molecular series emphasizing their overlap with other glioneuronal tumors
36. BRAIN METASTASIS OF A UROTHELIAL NEUROENDOCRINE CARCINOMA: A DOUBLE PITFALL FOR NEUROPATHOLOGISTS AND DNA‐METHYLATION PROFILING
37. Brainstem oligodendroglioma, IDH-mutant, and 1P/19Q-codeleted
38. Brain metastasis of a urothelial neuroendocrine carcinoma: A double pitfall for neuropathologists and DNA‐methylation profiling.
39. The pontine diffuse midline glioma, EGFR‐subtype with ependymal features: Yet another face of diffuse midline glioma, H3K27‐altered
40. The pontine diffuse midline glioma, EGFR‐subtype with ependymal features: Yet another face of diffuse midline glioma, H3K27‐altered.
41. NTRK ‐rearranged spindle cell neoplasms are ubiquitous tumours of myofibroblastic lineage with a distinct methylation class
42. A comprehensive analysis of infantile central nervous system tumors to improve distinctive criteria for infant‐type hemispheric glioma versus desmoplastic infantile ganglioglioma/astrocytoma.
43. Pediatric spinal pilocytic astrocytomas form a distinct epigenetic subclass from pilocytic astrocytomas of other locations and diffuse leptomeningeal glioneuronal tumours
44. An extracranial CNS presentation of the emerging “intracranial” mesenchymal tumor, FET: CREB-fusion positive
45. The genomic landscape of dysembryoplastic neuroepithelial tumours and a comprehensive analysis of recurrent cases
46. La classification de l’OMS 2021 des tumeurs du système nerveux central
47. A potential diagnostic pitfall: Primary synovial sarcoma of the central nervous system
48. Additional file 1 of Posterior fossa ependymoma H3 K27-mutant: an integrated radiological and histomolecular tumor analysis
49. Additional file 2 of Posterior fossa ependymoma H3 K27-mutant: an integrated radiological and histomolecular tumor analysis
50. A novel LARGE1-AFF2 fusion expanding the molecular alterations associated with the methylation class of neuroepithelial tumors with PATZ1 fusions
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