Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Barbara Adler-Brecher"'
Autor:
Nancy Durning, Maridel Tenned, Scott D. Rowley, Melanie Hankewycz, Dawn Wakefield, Michele L. Donato, Ann Ferolin-Ocot, Gabrielle Marczewski, Elana Smilow, Jennifer Krajewski, Alfred P. Gillio, Angelica Panganiban, Claritza Sanabria, Katayoon Modjarrad-Shaw, Jacklyn Russo, Barbara Adler-Brecher
Publikováno v:
Biology of Blood and Marrow Transplantation. 26:S292-S293
Background KIR B(x) haplotype donors have been reported to improve outcomes in patients (pts) receiving unrelated donors (URD) for myeloid malignancies, non-Hodgkin's lymphoma (NHL) and multiple myeloma (MM). Donors are categorized as KIR “Best”
Autor:
Andrew L. Pecora, Michele L. Donato, Ling Cai, Melissa Baker, Daniel Kim, Scott D. Rowley, David H. Vesole, Barbara Adler-Brecher, Hongkun Wang, Alan P Skarbnik
Publikováno v:
Biology of Blood and Marrow Transplantation. 22:2047-2055
Most patients eligible for allogeneic hematopoietic stem cell transplantation will require identification of an alternate (unrelated or mismatched related) donor. We explored the transplantation outcomes for a sequential series of 54 patients undergo
Autor:
Melanie Hankewycz, Shreya Agarwal, Krupesh Patel, Jennifer Krajewski, Nancy Durning, Alfred P. Gillio, Jeanette Haugh, Barbara Adler-Brecher
Publikováno v:
Biology of Blood and Marrow Transplantation. 24:S332
Autor:
Jeanette Haugh, Barbara Adler-Brecher, Alfred P. Gillio, Jennifer Krajewski, Melanie Hankewycz, Nancy Durning, Natasha Piracha
Publikováno v:
Biology of Blood and Marrow Transplantation. 22:S347
Autor:
Alfred P. Gillio, Anna Butturini, Barbara Adler-Brecher, Robert Peter Gale, Arleen D. Auerbach, Peter C. Verlander
Publikováno v:
Blood. 84:1650-1655
(95% confidence interval, 93% to 99%) by 40 years of age. Common hematologic abnormalities were thrombocytopenia and pancytopenia. These were often associated with decreased bone marrow (BM) cellularity (75% of cases studied). Clonal cytogenetic abno
Autor:
Philip F. Giampietro, Jessica G. Davis, Barbara Adler-Brecher, Peter C. Verlander, Arleen D. Auerbach, Steven G. Pavlakis
Publikováno v:
Pediatrics. 91:1116-1120
Objective. The objective of this study was to address the need for early diagnosis of Fanconi anemia (FA), an autosomal recessive chromosomal instability syndrome characterized by a unique cellular hypersensitivity to DNA cross-linking agents, such a
Autor:
Melissa Baker, Brenda Diaz, Pamela Sutherland, Michele L. Donato, Barbara Adler-Brecher, Daniel Kim, Scott D. Rowley, Michele Boonstra, David H. Vesole, Andrew L. Pecora, Phyllis McKiernan, Alan P Skarbnik
Publikováno v:
Blood. 124:1226-1226
Haploidentical (HAPLO) and unrelated donors (URD) are established cell sources for patients (pts) who lack HLA-matched siblings. Limited data are available comparing transplant (TP) outcomes using cells from HAPLO vs URD donors. We performed a retros
Autor:
Barbara Adler Brecher, Stuart L. Goldberg, Phyllis McKiernan, Scott D. Rowley, Jack S. Hsu, Andrew L. Pecora, Kelly Kobbe, Robert A. Preti, Linda Butrin
Publikováno v:
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 10(11)
Hematopoietic stem cell chimerism can be established after low-dose conditioning regimens, although the risk of donor cell rejection increases for unrelated donor transplantations. We added pretransplantation rabbit antithymocyte globulin (6 mg/kg) t
Autor:
Andre Goy, Eiswarya Chichili, Michele L. Donato, Elizabeth Bilotti, Melissa Baker, David S. Siegel, Andrew L. Pecora, Phyllis McKiernan, David H. Vesole, Scott D. Rowley, Barbara Adler-Brecher, Themba Nyirenda
Publikováno v:
Blood. 118:4162-4162
Abstract 4162 Allogeneic hematopoietic stem cell transplantation has been associated with a graft-versus-myeloma effect and may be the only potentially curative option for patients with advanced multiple myeloma. Unfortunately, the majority of patien
Autor:
R.G. Allen, William R. Mann, Drew A. Olsen, Barbara Weiffenbach, Jen-I Mao, Barbara Adler-Brecher, Arleen D. Auerbach, Qian Liu, Stephanie L. Sherman, V.S. Venkatraj
Publikováno v:
Genomics. 9(2)
Fanconi anemia is a rare autosomal recessive disorder in which affected individuals are predisposed to acute myelogenous leukemia and other malignancies. We report the results of a genetic linkage study involving 34 families enrolled in the Internati