Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Martin J. Inwood"'
Publikováno v:
Canadian Journal of Infectious Diseases, Vol 5, Iss 1, Pp 33-36 (1994)
Classically, a swollen, painful joint in a patient with hemophilia has been considered to be due to a hemarthrosis until otherwise proven, and treated immediately with appropriate coagulation factor replacement. Two cases of human immunodeficiency vi
Externí odkaz:
https://doaj.org/article/c4afd3208ba64ab8b85f53443196e59e
Autor:
Barbara A. Konkle, Joseph Addiego, Benjamin Deulbesonic, George R. Buchanan, Brad Lewis, Linda G. Shaffer, Alton L. Lightsey, Ari J. Cohen, W. Keith Hoots, James L. Harper, John Bouhasin, Thomas H. Howard, Donald Mahoney, Gilbert C. White, Parvin Saidi, Carol K. Kasper, D. C. Talbert, Eric Larsen, David Lilligrap, Jack Lazerson, Martin J. Inwood, Bruce Ritchie, Elizabeth Kurczynski, Margaret Heisel, James Harper, J. Paul Scott, Robert L. Janco, Peter A. Kouides, Frederick Rickles, Alan Cohen, Anne Thomas, Indira Warrier, Prad Phatak, John D. Bouhasin, Cathy Rosenfield, S. R. Seitcher, David Green, Deborah L Brown, J. Heinreich Joist, Bridget Freeman, Mark Mancino, Edward H. Romond, Felicia Little, Leticia Valdez, Eric J. Werner, Patricia McCusker, Robert Bona, W. Paul Bowman, Louis Geeraerts, J. Teitel, Donna DiMichele, Catherine S. Manno, Jerry S. Powell, Bruce M. Ewenstein, Michael D. Tarantino, Dennis Gastineau, Richard Edwards, Thomas C. Abshire, Craig M. Kessler, Rachelle Nuss, Judy Wilimas, Gerald Gilchrist, Cindy Lessinger, Roshini Kulkarni, Jeannne M. Lusher, Margaret V. Ragni, Alberao Pappo, Sarah Hawk, Georges E. Rivard, Man Chiu Poon
Publikováno v:
Haemophilia. 7:235-241
The optimal treatment of patients with von Willebrand's disease (vWD) remains to be defined. Moreover, it has not been firmly established which, if any, commonly measured parameters of von Willebrand factor (vWF) protein in the plasma are useful in g
Autor:
Margaret Adams, Victor S. Blanchette, Irwin Walker, Robin S. Roberts, Peter Gill, Martin J. Inwood
Publikováno v:
Transfusion Medicine Reviews. 8:210-217
Autor:
Richard S. Schwartz, Charles F. Abildgaard, Louis M. Aledort, Steven Arkin, Arthur L. Bloom, Hans H. Brackmann, Doreen B. Brettler, Hiromu Fukui, Margaret W. Hilgartner, Martin J. Inwood, Carol K. Kasper, Peter B.A. Kernoff, Peter H. Levine, Jeanne M. Lusher, Pier M. Mannucci, Inge Scharrer, Mary A. MacKenzie, Nazreen Pancham, Harng S. Kuo, Randy U. Allred
Publikováno v:
New England Journal of Medicine. 323:1800-1805
Background. Current treatment of hemophilia A, a hereditary disorder affecting approximately 1 in 10,000 males, relies on plasma-derived factor VIII concentrates. We tested the safety and efficacy of a recombinant factor VIII preparation for the trea
Publikováno v:
Canadian Journal of Infectious Diseases, Vol 5, Iss 1, Pp 33-36 (1994)
Classically, a swollen, painful joint in a patient with hemophilia has been considered to be due to a hemarthrosis until otherwise proven, and treated immediately with appropriate coagulation factor replacement. Two cases of human immunodeficiency vi
Autor:
Martin J. Inwood, Jeanne M. Lusher
Publikováno v:
Transfusion medicine reviews. 6(4)
Publikováno v:
DICP : the annals of pharmacotherapy. 24(9)
The formulation of an oral iron tablet may influence its therapeutic efficacy in correcting iron deficiency. In order to determine the oral iron preparations patients in a Canadian urban center were receiving, a questionnaire was circulated to family
Autor:
Martin J. Inwood, Ivan T. Borda
Publikováno v:
Gastroenterology. 106:281
Autor:
Martin J. Inwood
Publikováno v:
Archives of Internal Medicine. 153:263
I was most interested to read the continuing correspondence in the January 1992 issue of theArchivesconcerning the above subject and the complications of hematoma formation experienced with subcutaneous heparin injections. 1 In my experience, a major
Autor:
William F. Brien, Martin J. Inwood
Publikováno v:
Thrombosis and Haemostasis. 67:282-282