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

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

5. Impact of age on survival according to molecular tumor findings in children and adolescents with soft-tissue and bone sarcoma: The BIOSCA project

7. Alveolar soft part sarcomas in young patients: The French national NETSARC+ network experience

9. 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. Reversible transitions between noradrenergic and mesenchymal tumor identities define cell plasticity in neuroblastoma

13. Leiomyosarcoma and liposarcoma in young patients: The national netsarc+ network experience

16. Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding

17. Breast carcinomas with osteoclast-like giant cells: a comprehensive clinico-pathological and molecular portrait and evidence of RANK-L expression

19. Oncogenic chimeric transcription factors drive tumor-specific transcription, processing, and translation of silent genomic regions

20. NUT carcinoma in children, adolescents and young adults

21. First-in-child phase I/II study of the dual mTORC1/2 inhibitor vistusertib (AZD2014) as monotherapy and in combination with topotecan-temozolomide in children with advanced malignancies: arms E and F of the AcSé-ESMART trial

25. New Born and Infant Soft Tissue Sarcomas

26. A Clinico-Genetic Score Incorporating Disease-Free Intervals and Chromosome 8q Copy Numbers: A Novel Prognostic Marker for Recurrence and Survival Following Liver Resection in Patients with Liver Metastases of Uveal Melanoma.

27. NFATc2-rearranged sarcomas: clinicopathologic, molecular, and cytogenetic study of 7 cases with evidence of AGGRECAN as a novel diagnostic marker

30. A subset of epithelioid and spindle cell rhabdomyosarcomas is associated with TFCP2 fusions and common ALK upregulation

32. Imaging characterization of paediatric tumours with the neurotrophic tyrosine receptor kinase fusion transcript

34. SHH medulloblastoma in a young adult with a TCF4 germline pathogenic variation

35. Relevance of a molecular tumour board (MTB) for patients’ enrolment in clinical trials: experience of the Institut Curie

36. The EP300:BCOR fusion extends the genetic alteration spectrum defining the new tumoral entity of “CNS tumors with BCOR internal tandem duplication”

39. Does ATRX germline variation predispose to osteosarcoma? Three additional cases of osteosarcoma in two ATR-X syndrome patients

41. Neurotrophic tropomyosin receptor kinase (NTRK) fusion positive tumors: a historical cohort analysis

42. Fat-Containing Soft Tissue Tumors in Children, Adolescents, and Young Adults: Which Require Biopsy?

43. Clinical effect of molecular methods in sarcoma diagnosis (GENSARC): a prospective, multicentre, observational study

49. Reversible transitions between noradrenergic and mesenchymal tumor identities define cell plasticity in neuroblastoma

50. Supplementary Table S1 from Integrated Genomic and Transcriptomic Analysis of Ductal Carcinoma In situ of the Breast

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