718 results on '"Riedel, Richard"'
Search Results
252. Clinical characteristics and treatment outcome of patients with advanced non-small-cell lung cancer (NSCLC) and FGFR fusions.
253. Impact of nirogacestat on pain, a key symptom in patients with desmoid tumors (DT): Results from the phase 3 DeFi study.
254. Tumor volume and T2 hyperintensity changes from DeFi: A phase 3, randomized, controlled trial of nirogacestat in patients with desmoid tumors.
255. A multicenter phase II study of cabozantinib + nivolumab for patients (pts) with advanced angiosarcoma (AS) previously treated with a taxane (Alliance A091902).
256. Primary Meningeal Rhabdomyosarcoma
257. Neutron Scattering Experiment Automation with Python
258. Abstract SY36-03: Intraoperative molecular imaging with protease-activated fluorescent imaging agents
259. Effects of enhanced caregiver training program on cancer caregiver’s self-efficacy, preparedness, and psychological well-being
260. Faculty Opinions recommendation of The hepatocyte growth factor receptor as a potential therapeutic target for dedifferentiated liposarcoma.
261. SARC 028: A phase II study of the anti-PD1 antibody pembrolizumab (P) in patients (Pts) with advanced sarcomas.
262. A phase Ib dose-escalation study of TRC105 (anti-endoglin antibody) in combination with pazopanib in patients with advanced soft tissue sarcoma (STS).
263. Soft Tissue Sarcoma: Clinical Practice Guidelines in Oncology
264. In vitro and in vivo anti-inflammatory activity of the new glucocorticoid ciclesonide
265. Early palliative care on an inpatient oncology unit: Impact of a novel co-rounding partnership on patient and health system outcomes.
266. Faculty Opinions recommendation of Phase II study of the safety and antitumor activity of the hypoxia-activated prodrug TH-302 in combination with doxorubicin in patients with advanced soft tissue sarcoma.
267. Gastrointestinal Stromal Tumors, Version 2.2014
268. A phase I study of the safety and activation of a cathepsin-activatable fluorescent cancer-specific probe LUM015.
269. Soft Tissue Sarcoma, Version 2.2014
270. Faculty Opinions recommendation of Vincristine, irinotecan, and temozolomide in patients with relapsed and refractory Ewing sarcoma.
271. Cross Species Genomic Analysis Identifies a Mouse Model as Undifferentiated Pleomorphic Sarcoma/Malignant Fibrous Histiocytoma
272. Abstract C61: Phase I Study of pazopanib in combination with the investigational hypoxia-targeted drug TH-302.
273. Faculty Opinions recommendation of An open-label, phase 2 study evaluating the efficacy and safety of the anti-IGF-1R antibody cixutumumab in patients with previously treated advanced or metastatic soft-tissue sarcoma or Ewing family of tumours.
274. Results of an International Randomized Phase III Trial of the Mammalian Target of Rapamycin Inhibitor Ridaforolimus Versus Placebo to Control Metastatic Sarcomas in Patients After Benefit From Prior Chemotherapy
275. Oncologists’ perceptions of rounding alongside palliative care physicians: Results of a post-intervention survey study.
276. Sharing the Sandbox: Implementation and Results From a Fully Integrated Palliative Care/Medical Oncology Rounding Model for Inpatient Cancer Care (SA512)
277. Improvement in Patient and Health System Outcomes With an Integrated Oncology and Palliative Medicine Inpatient Rounding Service (S733)
278. Faculty Opinions recommendation of Systemic analysis of gene expression profiles identifies ErbB3 as a potential drug target in pediatric alveolar rhabdomyosarcoma.
279. Lung.
280. Pathologic Complete Response of a Malignant Peripheral Nerve Sheath Tumor in the Lung Treated With Neoadjuvant Ifosfamide and Radiation Therapy
281. Faculty of 1000 evaluation for Adjuvant chemotherapy with doxorubicin, ifosfamide, and lenograstim for resected soft-tissue sarcoma (EORTC 62931): a multicentre randomised controlled trial.
282. Soft Tissue Sarcoma, Version 2.2012
283. Targeted Therapy in Sarcoma: Should We Be Lumpers or Splitters?
284. A phase I study of bevacizumab, everolimus and panitumumab in advanced solid tumors
285. Phase III, placebo-controlled trial (SUCCEED) evaluating ridaforolimus as maintenance therapy in advanced sarcoma patients following clinical benefit from prior standard cytotoxic chemotherapy: Long-term (≥ 24 months) overall survival results.
286. Faculty Opinions recommendation of Insulin growth factor-receptor (IGF-1R) antibody cixutumumab combined with the mTOR inhibitor temsirolimus in patients with refractory Ewing's sarcoma family tumors.
287. Faculty Opinions recommendation of NY-ESO-1 is a ubiquitous immunotherapeutic target antigen for patients with myxoid/round cell liposarcoma.
288. Faculty Opinions recommendation of Expression of therapeutic targets in Ewing sarcoma family tumors.
289. Efficacy of Phosphatidylinositol-3 Kinase Inhibitors in a Primary Mouse Model of Undifferentiated Pleomorphic Sarcoma
290. Abstract B58: Phase I study of the IGF-1R antibody ganitumab (AMG 479) in combination with everolimus in patients with advanced solid tumors.
291. Faculty Opinions recommendation of Natural history of imatinib-naive GISTs: a retrospective analysis of 929 cases with long-term follow-up and development of a survival nomogram based on mitotic index and size as continuous variables.
292. Targeted Agents for Sarcoma: Is Individualized Therapy Possible in Such a Diverse Tumor Type?
293. Variable acoustics at hauppauge high school
294. Faculty Opinions recommendation of Activity of Sorafenib against desmoid tumor/deep fibromatosis.
295. Faculty Opinions recommendation of Identification of an inhibitor of the EWS-FLI1 oncogenic transcription factor by high-throughput screening.
296. Fall- and Spring-sown Cover Crop Mulches Affect Yield, Fruit Cleanliness, and Fusarium Fruit Rot Development in Pumpkin
297. Four-circle single-crystal neutron diffractometer at the High Flux Isotope Reactor
298. Emerging Therapeutic Targets for Soft Tissue Sarcoma
299. Faculty Opinions recommendation of Testosterone regulates cell proliferation in aggressive fibromatosis (desmoid tumour).
300. Faculty Opinions recommendation of Clinical features and outcomes in patients with extraskeletal ewing sarcoma.
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