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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

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

10. CNS neuroblastoma, FOXR2-activated and its mimics: a relevant panel approach for work-up and accurate diagnosis of this rare neoplasm

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

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

20. Clinicopathological and molecular characterization of three cases classified by DNA-methylation profiling as “Glioneuronal Tumors, NOS, Subtype A”

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.

27. The dural angioleiomyoma harbors frequent GJA4 mutation and a distinct DNA methylation profile

29. Disseminated diffuse midline gliomas, H3K27-altered mimicking diffuse leptomeningeal glioneuronal tumors: a diagnostical challenge!

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

45. The genomic landscape of dysembryoplastic neuroepithelial tumours and a comprehensive analysis of recurrent cases

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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