T
Thomas Ed
Researcher at University of Washington
Publications - 398
Citations - 46691
Thomas Ed is an academic researcher from University of Washington. The author has contributed to research in topics: Transplantation & Leukemia. The author has an hindex of 103, co-authored 384 publications receiving 45502 citations. Previous affiliations of Thomas Ed include United States Department of Veterans Affairs & Fred Hutchinson Cancer Research Center.
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Journal Article
1994 Consensus Conference on Acute GVHD Grading.
Donna Przepiorka,Daniel J. Weisdorf,Paul J. Martin,Hans G. Klingemann,Beatty P,Hows J,Thomas Ed +6 more
TL;DR: Reports of GVHD prevention trials should include an accurate description of the grading system used and should report actuarial rates of grades II-IV and III-IV GV HD corrected for graft failure and potential interventions for early relapse.
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Clinical manifestations of graft-versus-host disease in human recipients of marrow from HL-A-matched sibling donors.
Glucksberg H,Rainer Storb,Alexander Fefer,C. D. Buckner,Paul E. Neiman,Clift Ra,Lerner Kg,Thomas Ed +7 more
TL;DR: The results show that despite histocompatibility matching and methotrexate therapy, GVHD remains a serious and often fatal complication of marrow transplantation.
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Reconstitution of cellular immunity against cytomegalovirus in recipients of allogeneic bone marrow by transfer of T-cell clones from the donor
Elizabeth A. Walter,Phil Greenberg,Mark J. Gilbert,R. J. Finch,Kathe S. Watanabe,Thomas Ed,Stanley R. Riddell +6 more
TL;DR: The transfer of CMV-specific clones of CD8+ T cells derived from the bone marrow donor is a safe and effective way to reconstitute cellular immunity against CMV after allogeneic marrow transplantation.
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Bone-marrow transplantation (first of two parts).
Thomas Ed,Rainer Storb,Clift Ra,Alexander Fefer,F. L. Johnson,Paul E. Neiman,Lerner Kg,Glucksberg H,C. D. Buckner +8 more
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Antileukemic Effect of Graft-versus-Host Disease in Human Recipients of Allogeneic-Marrow Grafts
TL;DR: The apparent antileukemic effect was more marked in patients with lymphoblastic than nonlymphoblastic leukemia, and in those who received transplants during relapse rather than during remission, and was most evident during the first 130 days after transplantation.