999 results on '"Collini, Paola"'
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2. Radiomic features of primary retroperitoneal sarcomas: a prognostic study
3. Timeline of surgery in localized angiosarcoma of the breast: Improving outcome following multidisciplinary treatment optimization
4. Spatial distribution of tumour immune infiltrate predicts outcomes of patients with high-risk soft tissue sarcomas after neoadjuvant chemotherapy
5. Clinical recommendations for treatment of localized angiosarcoma: A consensus paper by the Italian Sarcoma Group
6. A Gradual Transition Toward Anaplasia in Wilms Tumor Through Tolerance to Genetic Damage
7. Regorafenib in advanced solitary fibrous tumour: Results from an exploratory phase II clinical study
8. Secondary osteosarcoma: a challenge indeed
9. Thyroid Carcinomas
10. Cutaneous Melanoma
11. Epidemiology and Differential Diagnosis of Cutaneous Tumors
12. Gene expression-based dissection of inter-histotypes, intra-histotype and intra-tumor heterogeneity in pediatric tumors
13. Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility
14. Analysis of the mutational status of SIX1/2 and microRNA processing genes in paired primary and relapsed Wilms tumors and association with relapse
15. ISG15 as a prognostic biomarker in solitary fibrous tumour
16. Diagnostic yield and accuracy of image-guided percutaneous core needle biopsy of paediatric solid tumours: An experience from Italy
17. Pazopanib for treatment of typical solitary fibrous tumours: a multicentre, single-arm, phase 2 trial
18. Rechallenge of denosumab in jaw osteonecrosis of patients with unresectable giant cell tumour of bone: a case series analysis and literature review
19. Chromosomal anomalies at 1q, 3, 16q, and mutations of SIX1 and DROSHA genes underlie Wilms tumor recurrences
20. Wilms tumor, medulloblastoma, and rhabdomyosarcoma in adult patients: lessons learned from the pediatric experience
21. Paediatric Tumours of Neuroendocrine/Peripheral Neuroectodermal Origin
22. Pazopanib for treatment of advanced extraskeletal myxoid chondrosarcoma: a multicentre, single-arm, phase 2 trial
23. Gradual transition towards anaplasia in Wilms tumor through tolerance to genetic damage
24. Non-Rhabdomyosarcoma Soft Tissue Sarcomas
25. Intraperitoneal Invasion of Retroperitoneal Sarcomas: A Risk Factor for Dismal Prognosis
26. Anthracycline-based and gemcitabine-based chemotherapy in the adjuvant setting for stage I uterine leiomyosarcoma: a retrospective analysis at two reference centers
27. Effectiveness of irinotecan plus trabectedin in a desmoplastic small round cell tumor patient-derived xenograft
28. Abstract 6726: Effectiveness of irinotecan plus trabectedin in a desmoplastic small round cell tumor patient-derived xenograft
29. Abstract 2245: The transcriptomic profile of retroperitoneal primary well differentiated liposarcoma (WDLPS) and well differentiated (WD)/dedifferentiated (DD) components of DD liposarcoma (DDLPS) reveals the progression from WDLPS to DDLPS
30. Supplementary Table S4 from Predictive Value of MRP-1 in Localized High-Risk Soft Tissue Sarcomas: A Translational Research Associated to ISG-STS 1001 Randomized Phase III Trial
31. Data from Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST
32. Supplementary Data from Predictive Value of MRP-1 in Localized High-Risk Soft Tissue Sarcomas: A Translational Research Associated to ISG-STS 1001 Randomized Phase III Trial
33. Revised supplementary Figure 1 from Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST
34. Revised supplementary Figure 2 from Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST
35. Revised supplementary Table 1 from Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST
36. Revised supplementary Table 4 from Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST
37. Revised supplementary Table 2 from Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST
38. Revised supplementary Table 3 from Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST
39. Supplementary Figure S1 from Addition of Antiestrogen Treatment in Patients with Malignant PEComa Progressing to mTOR Inhibitors
40. Supplementary Table S1 from Addition of Antiestrogen Treatment in Patients with Malignant PEComa Progressing to mTOR Inhibitors
41. Supplementary Table S1 from Role of Chemotherapy, VEGFR Inhibitors, and mTOR Inhibitors in Advanced Perivascular Epithelioid Cell Tumors (PEComas)
42. Supplementary Figure S2 from Role of Chemotherapy, VEGFR Inhibitors, and mTOR Inhibitors in Advanced Perivascular Epithelioid Cell Tumors (PEComas)
43. Data from Mutation-Independent Anaplastic Lymphoma Kinase Overexpression in Poor Prognosis Neuroblastoma Patients
44. Supplementary Methods, Figures 1-4, Tables 1-3 from Mutation-Independent Anaplastic Lymphoma Kinase Overexpression in Poor Prognosis Neuroblastoma Patients
45. Treating secondary malignant neoplasms: A burden of childhood cancer survivors
46. Long‐term survivors with desmoplastic small round cell tumor ( DSRCT ): Results from a retrospective single‐institution case series analysis
47. Neuroblastoma (Peripheral neuroblastic tumours)
48. The role of S100a4 (Mts1) in Apc- and Smad4-driven tumour onset and progression
49. Rhabdomyosarcoma in adults: analysis of treatment modalities in a prospective single-center series
50. Pathological and radiological response following neoadjuvant treatments in primary localized resectable myxofibrosarcoma and undifferentiated pleomorphic sarcoma of the extremities and trunk wall.
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