Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Debra Frei-Lahr"'
Publikováno v:
Pharmacotherapy. 25:1134-1140
Fortunately, the occurrence of acute myeloid leukemia (AML) during pregnancy is rare. We report a case of successful fetal outcome with standard induction and consolidation treatment in the second and third trimesters, respectively. A 37-year-old wom
Publikováno v:
Transplantation Proceedings. 35:3089-3092
As the life expectancy of patients with homozygous sickle cell anemia (SCA) improves, SCA care providers are confronted with diseases of the adult SCA population rarely seen before. We report here a 40-year-old woman with SCA who developed diffuse la
Autor:
Camille N. Abboud, Michael Macri, Scott E. Cruickshank, Dora Menchaca, Debra Frei-Lahr, Edmund K. Waller, Michael W. Schuster, Roy A. Beveridge, Jeannine T. Holden
Publikováno v:
Experimental Hematology. 30:1044-1050
To assess the safety and efficacy of pegylated recombinant human megakaryocyte growth and development factor (PEG-rHuMGDF) administered after autologous bone marrow transplantation (ABMT).Two randomized, double-blind, placebo-controlled studies were
Publikováno v:
American Journal of Hematology. 57:326-330
A patient with multiple myeloma was noted to have an IgA deficiency during investigation of a possible transfusion reaction due to IgA deficiency and anti-IgA. Because of the patient's age, otherwise good health, and early stage of disease, he was en
Autor:
Debra Frei-Lahr, Lise Hoffmann, Geoffrey P. Herzig, Neal P. Christiansen, Jesper Jurlander, Matthew P. Strout, Maria R. Baer, Edward D. Ball, Tapani Ruutu, Adam R. Oberkircher, Clara D. Bloomfield, Sakari Knuutila, AnneMarie W. Block, Michael A. Caligiuri
Publikováno v:
Blood. 88:2183-2191
The AML1/ETO fusion transcript is expressed in virtually all patients with t(8;21) (q22;q22) acute myeloid leukemia (AML). The fusion transcript can be detected by reverse transcription-polymerase chain reaction (RT-PCR) in most of these patients in
Autor:
Michael Dale Lairmore, Nancy Vander Heyden, Elizabeth Paine, Debra Frei-Lahr, Randy G. Brown, Satyanarayan Reddy, Paul J. Petruska, Lee Ratner
Publikováno v:
American Journal of Hematology. 34:215-222
Clinical and laboratory data are described for two siblings who both developed adult T-cell leukemia/lymphoma resulting from infection by human T lymphotropic virus type I (HTLV-I). These findings suggest that genetic factors or virus-specific factor
Autor:
Gabrielle Meyers, William Babcock, Yoshiko Murakami, Charles J. Parker, Ken Kurokawa, Junichi Nishimura, Yuzuru Kanakura, Taroh Kinoshita, Hiroaki Shime, Norimitsu Inoue, Debra Frei-Lahr, Takashi Machii, Yuichi Endo, Carl T. Wittwer, Tomohisa Izui-Sarumaru, Zhong Chen, Maki Kuwayama
Somatic mutation of PIGA in hematopoietic stem cells causes deficiency of glycosyl phosphatidylinositol–anchored proteins in paroxysmal nocturnal hemoglobinuria (PNH) that underlies the intravascular hemolysis but does not account for expansion of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83e853d9cc27f1d84f12cf78fe61b6fe
https://europepmc.org/articles/PMC1895453/
https://europepmc.org/articles/PMC1895453/
Publikováno v:
Pharmacotherapy. 26(6)
Rasburicase is currently approved at a dosage of 0.15-0.2 mg/kg once/day for 5 days in pediatric patients with cancer to lower plasma uric acid concentrations and manage tumor lysis syndrome (TLS). Information on rasburicase dosing in adults is limit
Publikováno v:
Southern medical journal. 95(9)
Primary mediastinal large B-cell lymphoma (PMLBCL) is a distinct disease entity that has a relatively short history. The prognosis and therapy of patients with PMLBCL is still controversial. We summarize our experience with PMLBCL at the Medical Univ
Publikováno v:
Journal of clinical apheresis. 6(1)
Hemolytic uremic syndrome/thrombotic thrombocytopenic purpura (HUS/TTP) is a rare and often fatal complication of bone marrow transplantation (BMT). In this study, we report eight such cases (seven allo and one auto) treated with plasma exchanges (PE