185 results on '"Ragnhammar P"'
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2. HER3 expression in patients with primary colorectal cancer and corresponding lymph node metastases related to clinical outcome
3. Treatment with GM-CSF and IL-2 in patients with metastatic colorectal carcinoma induced high serum levels of neopterin and sIL-2R, an indicator of immune suppression
4. Clinical effects of monoclonal antibody 17-1A combined with granulocyte/macrophage-colony-stimulating factor and interleukin-2 for treatment of patients with advanced colorectal carcinoma
5. Anti-tumoral effect of GM-CSF with or without cytokines and monoclonal antibodies in solid tumors
6. Neutralising antibodies to granulocyte-macrophage colony stimulating factor (GM-CSF) in carcinoma patients following GM-CSF combination therapy
7. Humoral anti-idiotypic and anti-anti-idiotypic immune response in cancer patients treated with monoclonal antibody 17-1A
8. Granulocyte/macrophage-colony-stimulating factor augments the induction of antibodies, especially anti-idiotypic antibodies, to therapeutic monoclonal antibodies
9. How to optimize the effect of 5-fluorouracil modulated therapy in advanced colorectal cancer
10. Cytotoxicity of white blood cells activated by granulocyte-colony-stimulating factor, granulocyte/macrophage-colony-stimulating factor and macrophage-colony-stimulating factor against tumor cells in the presence of various monoclonal antibodies
11. Induction of an immune network cascade in cancer patients treated with monoclonal antibodies (ab1): II. Is induction of anti-idiotype reactive T cells (T3) of importance for tumor response to mAb therapy?
12. Low dose cyclophosphamide, alpha-interferon and continuous infusions of interleukin-2 in advanced renal cell carcinoma
13. The therapeutic use of the unconjugated monoclonal antibodies (MAb) 17-1a in combination with GM-CSF in the treatment of COLORECTAL CARCINOMA (CRC)
14. Cytotoxic functions of blood mononuclear cells in patients with colorectal carcinoma treated with mAb 17-1A and granulocyte/macrophage-colony-stimulating factor
15. Chemotherapy and immunotherapy of colorectal cancer
16. Granulocyte-monocyte colony-stimulating-factor augments the interleukin-2-induced cytotoxic activity of human lymphocytes in the absence and presence of mouse or chimeric monoclonal antibodies (mAb 17-1A)
17. Ga733/EpCAM as a Target for Passive and Active Specific Immunotherapy in Patients with Colorectal Carcinoma
18. Production of neutralizing granulocyte-macrophage colony-stimulating factor (GM-CSF) antibodies in carcinoma patients following GM-CSF combination therapy
19. Incidence of GM-CSF Antibodies in Cancer Patients Receiving GM-CSF for Immunostimulation
20. The clinical use of monoclonal antibodies, MAb 17-1A, in the treatment of patients with metastatic colorectal carcinoma
21. Granulocyte-monocyte-colony-stimulating factor augments the cytotoxic capacity of lymphocytes and monocytes in antibody-dependent cellular cytotoxicity
22. Tumor Budding in Colorectal Cancer with Regards to Mismatch Repair Status – Prognostic Value?
23. Experience measuring antibodies to both drug and impurities and their clinical sequelae
24. 5-FU split dose; a phase I/II and pharmacokinetic study of a differentschedule of the Nordic regimen in advanced colorectal carcinoma.
25. Thymidylate synthase expression in colorectal cancer: a prognostic andpredictive marker of benefit from adjuvant fluorouracil-basedchemotherapy.
26. The Swedish Council on Technology Assessment in Health Care (SBU)systematic overview of chemotherapy effects in some major tumourtypes--summary and conclusions.
27. Incidence of GM-CSF antibodies in cancer patients receiving GM-CSF forimmunostimulation.
28. A systematic overview of chemotherapy effects in colorectal cancer.
29. A systematic overview of chemotherapy effects in urothelial bladdercancer.
30. A prospective study of the use of chemotherapy in Sweden and assessment ofthe use in relation to scientific evidence.
31. Incidence of GM-CSF antibodies in cancer patients receiving GM-CSF for immunostimulation.
32. Immunohistochemical test for MLH1 and MSH2 is an independent prognostic factor in sporadic colorectal cancer
33. Ga733/EpCAM as a Target for Passive and Active Specific Immunotherapy in Patients with Colorectal Carcinoma
34. 990 Treatment with a combination of mMAb17-1A, GM-CSF, alpha-interferon and 5-fluorouracil of patients with advanced colorectal carcinoma (CRC)
35. Idiotypic network responses and anti-idiotypes in cancer therapy.
36. PD-0016 - Tumor Budding in Colorectal Cancer with Regards to Mismatch Repair Status – Prognostic Value?
37. Humoral anti-idiotypic and anti-anti-idiotypic immune response in cancer patients treated with monoclonal antibody 17-1-A.
38. Colorectal cancer
39. COMBINING MAb 17–1A WITH GM-CSF AND IL-2 IN ADVANCED COLORECTAL CARCINOMA (CRC)
40. Immunohistochemical determination of thymidylate synthase in colorectal cancer—methodological studies
41. Epithelial cells in the bone marrow (BM) of colorectal carcinoma (CRC) patients: A tool to monitor immunotherapy?
42. DIFFERENT DOSE REGIMENS OF THE MOUSE MONOCLONAL-ANTIBODY 17-1A FOR THERAPY OF PATIENTS WITH METASTATIC COLORECTAL-CARCINOMA
43. Monoclonal antibodies and cytokines for treatment of metastatic colorectal carcinoma (CRC) patients. – Is the idiotypic network response an important effector function?
44. Different dose regimens of 5-fluorouracil and interferon-α in patients with metastatic colorectal carcinoma
45. Subcutaneous Interleukin-2 and Alpha-Interferon in Advanced Colorectal Carcinoma. - A Phase II Study
46. Induction of anti-recombinant human granulocyte-macrophage colony- stimulating factor (Escherichia coli-derived) antibodies and clinical effects in nonimmunocompromised patients
47. Induction of an immune network cascadein cancer patients treated with monoclonal antibodies (ab 1 )
48. Monoclonal antibodies in combination with cytokines in treatment of advanced colorectal carcinoma
49. Therapy of Colorectal Carcinoma with Monoclonal Antibodies (MAb17-1A) Alone and in Combination with Granulocyte Monocyte-Colony Stimulating Factor (GM-CSF)
50. Augmentation of the immune response with granulocyte-macrophage colony-stimulating factor and other hematopoietic growth factors.
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