J
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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Journal ArticleDOI
An International Real-World Analysis of Relapsed/Refractory Lymphoma Occurring During Pregnancy.
Faheem Farooq,Justin S. Brandt,Elyce Cardonick,Evgeniya Polushkina,Julie M. Vose,Saira Ahmed,Praveen Ramakrishnan Geethakumari,Adam J. Olszewski,Hesham A Yasin,Umar Farooq,Nada Hamad,Yong Lin,Charlotte Maggen,Robert Fruscio,Mina Mhallem Gziri,Karina Dahl Steffensen,Frédéric Amant,Andrew M. Evens +17 more
Journal ArticleDOI
The SALENTO prognostic model for limited-stage peripheral T-cell lymphoma from the International T-Cell Project Network.
Greg Hapgood,Monica Civallero,Yana Stepanishyna,Julie M. Vose,Maria Elena Cabrera,Ranjana H. Advani,Stefano Pileri,Martina Manni,Steven M. Horwitz,Francine M. Foss,Felicitas Hitz,John Radford,Ivan Dlouhy,Carlos S. Chiattone,Won Seog Kim,Tetiana Skrypets,Arnon Nagler,Judith Trotman,Stefano Luminari,Massimo Federico +19 more
TL;DR: In this article , the SALENTO model (Limited Stage Peripheral T Cell Lymphoma Prognostic Model) was developed to predict overall survival (OS) for the common nodal PTCL subtypes (PTCL-NOS, AITL, ALCL).
Journal ArticleDOI
Enrichment of innate immune cells from PBMC followed by triple cytokine activation for adoptive immunotherapy.
Zaid S Al-Kadhimi,Michael Callahan,Todd A. Fehniger,Kathryn E. Cole,Julie M. Vose,Steven Hinrichs +5 more
TL;DR: In this paper , microbead depletion of T-cells and B-cells has been used as a graft manipulation method to prevent graft versus host disease (GVHD) post haploidentical AHSCT.
Book ChapterDOI
Diagnosis and Treatment of Non-Hodgkin’s Lymphoma of Adults
TL;DR: The non-Hodgkin’s lymphomas represent a diverse group of neoplasms with many different clinical presentations, associated laboratory abnormalities, responsiveness to treatment, and clinical outcome; the cell of origin and stage of maturation arrest prior to uncontrolled proliferation are important to the understanding of this diversity.