Zobrazeno 1 - 10
of 201
pro vyhledávání: '"J. Lazerson"'
Autor:
A. Lightsey, L. Valdez, P. Chenaille, J. Sanders, N. Hakami, G. Rivard, K. McRedmond, T. John Gribble, S. Travis, V. Castle, M. Ragni, W. MacLaughlin, E. Czapek, P. Saidi, M. Koerper, Nigel S. Key, C. Manno, J. Cohen, J. Fahner, H. Stranczyniski, S. Adair, M. Hanna, M. Inwood, R. Seeler, D. Gnarra, P. De Alarcon, P. Phatak, B. L. Kroner, V. Anderson, E. Warner, A. Homans, Jeffrey H. Davis, M. Manco-Johnson, B. Ewenstein, Jorge Luiz Barbosa, P. Blatt, J. Lusher, Donna DiMichele, C. Johnson, R. Gruppo, P. Santiago-Borrero, G. Heggie, D. Barrand, J. Katz, M. Karpatkin, T. Loew, R. Kosinski, R. Dubowy, B. Konkle, M. Kajani, Casper Kasper, D. Lillicrap, S. Seremetis, M. Dugdale, Jonathan M. Ducore, J. Lazerson, J. Herst, P. Bockenstedt, Jerry S. Powell, C. Rosenfield, J. Hutter, S. Rubin, G. White, J. Addiego, J. Sexauer, W. Hanna, J. Teitel, P. Haut, G. Davignon, C. Kessler, J. Drown
Publikováno v:
Thrombosis and Haemostasis. 87:52-57
SummaryThe North American Immune Tolerance Registry was initiated to study of immune tolerance (ITT) in Canada and the United States with respect to: 1) therapeutic regimens in use for haemophilia A (HA) and B (HB) inhibitor patients; 2) therapeutic
Publikováno v:
Hospital practice (Office ed.). 28(9)
Autor:
J Lazerson, Y Barak, Eva C. Guinan, Kenneth I. Weinberg, K Williams, PP Dukes, C Lenarsky, Howard J. Weinstein, Stefan Siegel, Jorge A. Ortega
Publikováno v:
Blood. 71:226-229
Constitutional pure red cell aplasia (CPRCA) is a syndrome of failed erythropoiesis usually diagnosed within the first year of life. Four patients with CPRCA received transplants with marrow from their HLA- identical, mixed lymphocyte culture-nonreac
Publikováno v:
Blood. 71:344-348
During a 4-year multicenter cooperative study of acquired factor VIII inhibitors in persons with hemophilia A, new inhibitors were detected in 31 of 1,306 patients who entered the study without an inhibitor or the history of an inhibitor. The inciden
Publikováno v:
Journal of Clinical Investigation. 79:943-949
To explain the transient anemia and poikilocytosis seen during infancy in hereditary elliptocytosis (HE), we resealed erythrocyte (RBC) ghosts from affected children or their elliptocytic parents with 2,3-diphosphoglycerate (DPG) (0-8 mM), a compound
Ectopic Olfactory Neuroblastoma: Systematic Review of a Rare Clinical Entity among Sinonasal Tumors.
Autor:
Lui, Christopher G., Badash, Ido, Tang, Liyang, Mark, Michelle E., Batra, Pete S., Wrobel, Bozena B.
Publikováno v:
Journal of Neurological Surgery. Part B. Skull Base; Apr2024, Vol. 85 Issue 2, p109-118, 10p
Publikováno v:
Blood. 63(6)
A new type II variant form of von Willebrand's disease has been recognized in a mother and daughter who have bleeding manifestations typical of von Willebrand's disease. Laboratory findings include consistently prolonged bleeding times, with normal l
Publikováno v:
Birth defects original article series. 12(8)
Publikováno v:
Archives of physical medicine and rehabilitation. 65(10)
Arc-aggregation is a new graphic method of analysis of progressive loss of range of motion that can be applied to any diarthrodial joint undergoing a specific degenerative process. It is based on the premise that loss of motion (LOM) for a specific c
Autor:
C, Lenarsky, K, Weinberg, E, Guinan, P P, Dukes, Y, Barak, J, Ortega, S, Siegel, K, Williams, J, Lazerson, H, Weinstein
Publikováno v:
Blood. 71(1)
Constitutional pure red cell aplasia (CPRCA) is a syndrome of failed erythropoiesis usually diagnosed within the first year of life. Four patients with CPRCA received transplants with marrow from their HLA-identical, mixed lymphocyte culture-nonreact