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Julie M. Vose

Researcher at University of Nebraska Medical Center

Publications -  569
Citations -  51589

Julie M. Vose is an academic researcher from University of Nebraska Medical Center. The author has contributed to research in topics: Transplantation & Lymphoma. The author has an hindex of 97, co-authored 541 publications receiving 46915 citations. Previous affiliations of Julie M. Vose include Memorial Hospital of South Bend.

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Multiple Organ Dysfunction Syndrome in Bone Marrow Transplantation

TL;DR: Single organ dysfunction during BMT is a marker for a systemic abnormality that has a high likelihood of progressing to MODS, similar to that seen in other critically ill patient populations.
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Long-term update of a phase II study of rituximab in combination with CHOP chemotherapy in patients with previously untreated, aggressive non-Hodgkin's lymphoma

TL;DR: The long-term follow-up of patients in this phase II trial of rituximab with CHOP chemotherapy for previously untreated aggressive NHL demonstrates a high response rate, which remains very durable with high 5-year overall and progression-free survivals.
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High-dose therapy and autologous peripheral stem cell transplantation for patients with bone marrow metastases and relapsed lymphoma: an alternative to bone marrow purging.

TL;DR: Patients with relapsed lymphoma and bone marrow metastases who receive high dose therapy followed by peripheral stem cell transplantation can experience long-term event-free survival.
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Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma, Version 1.2015

TL;DR: This portion of the NCCN Guidelines for Non-Hodgkin's Lymphomas describes the recent specific to the incorporation of recently approved targeted therapies for the management of patients with newly diagnosed and relapsed or refractory CLL/SLL.
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Venous thromboembolism in patients with hematologic malignancy and thrombocytopenia.

TL;DR: Within the limits of this retrospective study, cautious use of prophylactic‐dose low‐molecular‐weight heparin (LMWH) may be safe in thrombocytopenic patients with hematologic malignancy‐associated VTE.