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2. Imaging features to distinguish posterior fossa ependymoma subgroups

3. A new subtype of diffuse midline glioma, H3 K27 and BRAF/FGFR1 co-altered: a clinico-radiological and histomolecular characterisation

4. PLAG1 fusions extend the spectrum of PLAG(L)-altered CNS tumors

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

10. CNS tumor with EP300::BCOR fusion: discussing its prevalence in adult population

11. Pediatric-type high-grade neuroepithelial tumors with CIC gene fusion share a common DNA methylation signature

16. Glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA): a molecularly distinct brain tumor type with recurrent NTRK gene fusions

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”

23. CNS tumors with PLAGL1-fusion: beyond ZFTA and YAP1 in the genetic spectrum of supratentorial ependymomas

24. CNS erythroblastic sarcoma: a potential emerging pediatric tumor type characterized by NFIA::RUNX1T1/3 fusions

28. A comprehensive histomolecular characterization of meningioangiomatosis: Further evidence for a precursor neoplastic lesion

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

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

34. The role of irinotecan-bevacizumab as rescue regimen in children with low-grade gliomas: a retrospective nationwide study in 72 patients

36. Utility of combining OLIG2 and SOX10 IHC expression in CNS tumours: promising biomarkers for subtyping paediatric‐ and adult‐type gliomas

37. LEF-1 immunohistochemistry, a better diagnostic biomarker than β-catenin for medulloblastoma, WNT-activated subtyping

38. “Hemispheric pilocytic astrocytoma” revisited: A comprehensive clinicopathological and molecular series emphasizing their overlap with other glioneuronal tumors

39. BRAIN METASTASIS OF A UROTHELIAL NEUROENDOCRINE CARCINOMA: A DOUBLE PITFALL FOR NEUROPATHOLOGISTS AND DNA‐METHYLATION PROFILING

40. A new subtype of diffuse midline glioma, H3 K27 and BRAF/FGFR1 co-altered: a clinico-radiological and histomolecular characterisation

41. Étude de l’item d’interférence dans un dossier de validation de méthode : cas de la coloration HPS après fixation en formol-zinc et comparaison à la fixation en formol tamponné à 4 %

42. Robot-Assisted Stereotactic Biopsies in 377 Consecutive Adult Patients with Supratentorial Diffuse Gliomas: Diagnostic Yield, Safety, and Postoperative Outcomes

44. Brain metastasis of a urothelial neuroendocrine carcinoma: A double pitfall for neuropathologists and DNA‐methylation profiling.

47. Brainstem oligodendroglioma, IDH-mutant, and 1P/19Q-codeleted

48. Imaging features to distinguish posterior fossa ependymoma subgroups

49. The histomolecular criteria established for adult anaplastic pilocytic astrocytoma are not applicable to the pediatric population

50. Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course

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