30 results on '"Terrier, P"'
Search Results
2. Quality of surgical margins and local recurrence in primary extremity soft tissue sarcoma (STS).
3. Metronomic oral cyclophosphamide (CPM) and prednisolone in elderly patients (pts) with inoperable or metastatic soft tissue sarcoma (STS).
4. Frequency of β-catenin heterozygous mutations in extra-abdominal fibromatosis as a surrogate marker for disease management
5. Effect of adjuvant chemotherapy on survival in FNCLCC grade 3 soft tissue sarcomas: A multivariate analysis of the French Sarcoma Group database
6. Detection of β-catenin mutations in primary extra-abdominal fibromatosis (EAF): An ancillary diagnostic tool
7. Isolated limb perfusion (ILP) in advanced soft tissue sarcomas (STS): What is the best timing of surgery?
8. Clinical responses and outcome of 110 consecutive isolated limb perfusion (ILP) with TNF-α and melphalan (M) for locally advanced soft tissue sarcomas (LASTS) of extremities at the Institut Gustave Roussy
9. Topoisomerase II-alpha (Top2A) and chromosome 17 abnormalities in locally advanced soft tissue sarcomas (LASTS)
10. Clear cell sarcoma (CCS) or malignant melanoma of soft parts: A retrospective clinicopathologic study of 52 cases
11. Localized myxoid/round cell liposarcoma in adult patients. IL6 protein expression analysis
12. Can ERCC1 and topoisomerase II-alpha predict histological response and outcome after induction chemotherapy in locally advanced soft tissue sarcomas (LASTS)?
13. Long term progression-free survival correlates with KIT/PDGFR mutational status in advanced GIST patients treated with imatinib (IM)
14. Extra-abdominal fibromatosis: Can aggressive management be avoided in a subgroup of patients?
15. A prospective database of 100 patients with locally soft tissue sarcoma (STS) treated by isolated limb perfusion with melphalan and TNFα 1mg
16. EGFR is frequently hyperexpressed in human malignant peripheral nerve sheath tumors (MPNST) and is preferentially localized in high grade areas
17. Dynamic contrast-enhanced Doppler ultrasound (DCE-US) is a useful radiological assessment to early predict the outcome of patients with gastrointestinal stromal tumors (GIST) treated with imatinib (IM)
18. BRAF and NRAS mutational status in clear cell sarcoma
19. Impact of age on treatment and survival in soft tissus sarcoma. A study of 1568 sarcomas from the French Sarcoma Group
20. Intensive induction chemotherapy (API-AI regimen) followed by conservative surgery in adult patients with locally advanced soft tissue sarcoma (STS): Survival is predicted by the histological response
21. Study of the prognostic value and chemosensitivity according to the type of translocation in synovial sarcoma
22. Intensive induction chemotherapy (API-AI regimen) followed by conservative surgery in adult patients with locally advanced soft tissue sarcoma (STS): Survival is predicted by the histological response
23. Intensive induction chemotherapy (CT) without methotrexate (MTX) in adult patients with localized osteosarcoma (LO): Updated results of the Institut Gustave Roussy phase II trial
24. Study of the prognostic value and chemosensitivity according to the type of translocation in synovial sarcoma
25. Intensive induction chemotherapy (CT) without methotrexate (MTX) in adult patients with localized osteosarcoma (LO): Updated results of the Institut Gustave Roussy phase II trial
26. Prognostic Factors in Primary Breast Sarcomas: A Series of Patients With Long-Term Follow-Up
27. Comparative study of the National Cancer Institute and French Federation of Cancer Centers Sarcoma Group grading systems in a population of 410 adult patients with soft tissue sarcoma.
28. Prognostic factors in adult patients with locally controlled soft tissue sarcoma. A study of 546 patients from the French Federation of Cancer Centers Sarcoma Group.
29. Combined systemic chemoimmunotherapy in advanced diffuse malignant mesothelioma. Report of a phase I-II study of weekly cisplatin/interferon alfa-2a.
30. Loss of heterozygosity of the RB gene is a poor prognostic factor in patients with osteosarcoma.
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