1,001 results on '"Lipton, Allan"'
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2. Experience with denosumab (XGEVA®) for prevention of skeletal-related events in the 10 years after approval
3. Fibrotic activity quantified in serum by measurements of type III collagen pro-peptides can be used for prognosis across different solid tumor types
4. Diagnostic delays in breast cancer among young women: An emphasis on healthcare providers
5. Beyond October, Beyond Pink: A Year-Round Revelation for Women's Breast Health
6. Cancer and Bone: Historical Perspective
7. The C-Terminal Intact Forms of Periostin (iPTN) Are Surrogate Markers for Osteolytic Lesions in Experimental Breast Cancer Bone Metastasis
8. Collagen fragments quantified in serum as measures of desmoplasia associate with survival outcome in patients with advanced pancreatic cancer
9. Supplementary Figures S1 and S2 and Supplementary Tables S1 and S2 from Changes in Bone Turnover Marker Levels and Clinical Outcomes in Patients with Advanced Cancer and Bone Metastases Treated with Bone Antiresorptive Agents
10. Allan Lipton_Conflict of Interest Form from Changes in Bone Turnover Marker Levels and Clinical Outcomes in Patients with Advanced Cancer and Bone Metastases Treated with Bone Antiresorptive Agents
11. Data from Changes in Bone Turnover Marker Levels and Clinical Outcomes in Patients with Advanced Cancer and Bone Metastases Treated with Bone Antiresorptive Agents
12. Data from Quantitation of p95HER2 in Paraffin Sections by Using a p95-Specific Antibody and Correlation with Outcome in a Cohort of Trastuzumab-Treated Breast Cancer Patients
13. Supplementary Data from Quantitation of p95HER2 in Paraffin Sections by Using a p95-Specific Antibody and Correlation with Outcome in a Cohort of Trastuzumab-Treated Breast Cancer Patients
14. CCR Translation for This Article from Quantitation of p95HER2 in Paraffin Sections by Using a p95-Specific Antibody and Correlation with Outcome in a Cohort of Trastuzumab-Treated Breast Cancer Patients
15. Supplementary Figures 1-2, Methods from Lactoferrin–Endothelin-1 Axis Contributes to the Development and Invasiveness of Triple-Negative Breast Cancer Phenotypes
16. Supplementary Figure 3 from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
17. Supplementary Figure 2 from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
18. Supplementary Figure 1 from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
19. Supplementary Figure Legends 1-5 from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
20. Supplementary Figure 4 from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
21. Data from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
22. Supplementary Methods from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
23. Supplementary Table 1 from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
24. Supplementary Figure 5 from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
25. Supplementary Table 2 from Trastuzumab Has Preferential Activity against Breast Cancers Driven by HER2 Homodimers
26. Data from Lactoferrin–Endothelin-1 Axis Contributes to the Development and Invasiveness of Triple-Negative Breast Cancer Phenotypes
27. Hypocalcaemia in patients with metastatic bone disease treated with denosumab
28. Impact of serum HER2, TIMP-1, and CAIX on outcome for HER2+ metastatic breast cancer patients: CCTG MA.31 (lapatinib vs. trastuzumab)
29. New Targeted Therapies for Bone Metastases
30. Bisphosphonate Treatment for Osteolytic Bone Metastases Associated with Renal Cell Carcinoma
31. The diagnosis and treatment of bone metastases in breast cancer
32. Circulating HER2/neu : Clinical Utility
33. Possible survival benefits from zoledronic acid treatment in patients with bone metastases from solid tumours and poor prognostic features—An exploratory analysis of placebo-controlled trials
34. Superiority of denosumab to zoledronic acid for prevention of skeletal-related events: A combined analysis of 3 pivotal, randomised, phase 3 trials
35. Antiresorptive Therapy in the Management of Cancer Treatment-Induced Bone Loss
36. Effect of bone metastasis on outcomes in the CCTG BR.34 phase II randomized trial of dual immune checkpoint inhibitor (ICI) treatment with or without chemotherapy in high-risk, stage IVA/B NSCLC.
37. Phase II study of sunitinib as maintenance therapy in patients with locally advanced or metastatic non-small cell lung cancer
38. Clinical development of anti-RANKL therapies for treatment and prevention of bone metastasis
39. Treatment Persistence With Monthly Zoledronic Acid is Associated With Lower Risk and Frequency of Skeletal Complications in Patients With Breast Cancer and Bone Metastasis
40. Consensus on the utility of bone markers in the malignant bone disease setting
41. Dosing of zoledronic acid throughout the treatment continuum in breast cancer
42. Anticancer evidence for zoledronic acid across the cancer continuum
43. Proceedings of the First Global Workshop on Breast Cancer: Pathways to the Evaluation and Clinical Development of Novel Agents for Breast Cancer
44. Metastasis and bone loss: Advancing treatment and prevention
45. SRC kinase inhibition: Targeting bone metastases and tumor growth in prostate and breast cancer
46. Antitumor Effects and Anticancer Applications of Bisphosphonates
47. Implications of Bone Metastases and the Benefits of Bone-Targeted Therapy
48. Abstract P5-13-10: Elevated plasma IL-8 predicts for reduced outcomes in CCTG MA.38, a phase 2 randomized trial of palbociclib in ER+/HER2- metastatic breast cancer patients
49. Safety, Pharmacokinetics, and Pharmacodynamics of the Insulin-Like Growth Factor Type 1 Receptor Inhibitor Figitumumab (CP-751,871) in Combination with Paclitaxel and Carboplatin
50. MP73-10 BONE TURNOVER MARKER LEVELS AND OUTCOMES IN MEN WITH PROSTATE CANCER AND BONE METASTASES TREATED WITH BONE ANTIRESORPTIVE AGENTS
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