His scientific interests lie mostly in Internal medicine, Surgery, Oncology, Bevacizumab and Chemotherapy. His Internal medicine research includes themes of Gastroenterology and Glioma. In his research on the topic of Surgery, Interim analysis, Hydroxycarbamide, Imatinib mesylate and Imatinib is strongly related with Tyrosine-kinase inhibitor.
His work carried out in the field of Oncology brings together such families of science as Astrocytoma, Retrospective cohort study, Epidermal growth factor receptor and Pharmacology. The various areas that James J. Vredenburgh examines in his Bevacizumab study include Vascular endothelial growth factor and Survival analysis. His Chemotherapy research is multidisciplinary, incorporating elements of Breast cancer, Tolerability and Gefitinib.
James J. Vredenburgh spends much of his time researching Internal medicine, Oncology, Surgery, Chemotherapy and Bevacizumab. His work deals with themes such as Gastroenterology and Glioma, which intersect with Internal medicine. As part of the same scientific family, James J. Vredenburgh usually focuses on Glioma, concentrating on Pathology and intersecting with Cancer research.
His work in Oncology covers topics such as Pharmacology which are related to areas like Erlotinib. His Chemotherapy study combines topics in areas such as Breast cancer, Metastatic breast cancer and Bone marrow. His study in Bevacizumab is interdisciplinary in nature, drawing from both Progressive disease, Clinical trial, Vascular endothelial growth factor, Radiosurgery and Glioblastoma.
The scientist’s investigation covers issues in Internal medicine, Oncology, Bevacizumab, Surgery and Temozolomide. He focuses mostly in the field of Internal medicine, narrowing it down to topics relating to Gastroenterology and, in certain cases, Neutropenia. His studies in Oncology integrate themes in fields like Pharmacokinetics, Adverse effect, Pathology, Recurrent glioblastoma and Glioblastoma.
His Bevacizumab study also includes
James J. Vredenburgh focuses on Bevacizumab, Internal medicine, Surgery, Oncology and Temozolomide. His Bevacizumab research includes elements of Perforation, Nuclear medicine, Confidence interval, Effective diffusion coefficient and Radiation therapy. His work in Phases of clinical research, Clinical endpoint, Neutropenia, Dacarbazine and Chemotherapy is related to Internal medicine.
His Surgery study incorporates themes from Gastroenterology and Glioma. His Oncology study combines topics from a wide range of disciplines, such as Glioblastoma, Toxicity and Retrospective cohort study. His research in Temozolomide intersects with topics in Proteasome inhibitor, Proteasome, Angiogenesis, Cell growth and Programmed cell death.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Bevacizumab Alone and in Combination With Irinotecan in Recurrent Glioblastoma
Henry S. Friedman;Michael D. Prados;Patrick Y. Wen;Tom Mikkelsen.
Journal of Clinical Oncology (2009)
Bevacizumab Plus Irinotecan in Recurrent Glioblastoma Multiforme
James J. Vredenburgh;Annick Desjardins;James E. Herndon;Jennifer Marcello.
Journal of Clinical Oncology (2007)
Phase II Trial of Bevacizumab and Irinotecan in Recurrent Malignant Glioma
James J. Vredenburgh;Annick Desjardins;James E. Herndon;Jeannette M. Dowell.
Clinical Cancer Research (2007)
Phase II Trial of Gefitinib in Recurrent Glioblastoma
Jeremy N. Rich;David A. Reardon;Terry Peery;Jeannette M. Dowell.
Journal of Clinical Oncology (2004)
Immunologic Escape After Prolonged Progression-Free Survival With Epidermal Growth Factor Receptor Variant III Peptide Vaccination in Patients With Newly Diagnosed Glioblastoma
John H. Sampson;Amy B Heimberger;Gary E. Archer;Kenneth D. Aldape.
Journal of Clinical Oncology (2010)
High-dose chemotherapy and autologous bone marrow support as consolidation after standard-dose adjuvant therapy for high-risk primary breast cancer.
W P Peters;M Ross;J J Vredenburgh;B Meisenberg.
Journal of Clinical Oncology (1993)
Tetanus toxoid and CCL3 improve dendritic cell vaccines in mice and glioblastoma patients
Duane A. Mitchell;Kristen A. Batich;Michael D. Gunn;Min-Nung Huang.
Nature (2015)
Multi-institutional use of defibrotide in 88 patients after stem cell transplantation with severe veno-occlusive disease and multisystem organ failure: response without significant toxicity in a high-risk population and factors predictive of outcome.
Paul G Richardson;Carol Murakami;Zhezhen Jin;Diane L Warren.
Blood (2002)
Molecularly targeted therapy for malignant glioma
Sith Sathornsumetee;David A. Reardon;Annick Desjardins;Jennifer A. Quinn.
Cancer (2007)
Comparative effects of granulocyte-macrophage colony-stimulating factor (GM-CSF) and granulocyte colony-stimulating factor (G-CSF) on priming peripheral blood progenitor cells for use with autologous bone marrow after high-dose chemotherapy.
William P. Peters;Gary Rosner;Maureen Ross;James Vredenburgh.
Blood (1993)
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