Zobrazeno 1 - 10
of 12
pro vyhledávání: '"A E, Mauser"'
Autor:
C.L. Eckhardt, J.I. Loomans, A.S. van Velzen, M. Peters, E.P. Mauser‐Bunschoten, R. Schwaab, M.G. Mazzucconi, A. Tagliaferri, B. Siegmund, S.E. Reitter‐Pfoertner, J.G. van der Bom, K. Fijnvandraat, P.W. Kamphuisen, K. Peerlinck, J. Oldenburg, E. Santagostino, J. Astermark, C.L Eckhardt, A.S van Velzen, N. Streefkerk, J.L. Loomans, A. van Eijkelenburg, A.J. Jansen, C.C. Kruijt, B. van Tienoven, A.C.G. van Baar, I.W. Corten, K. Meijer, M.R. Nijziel, N. Dors, K. Hamulyak, E. Beckers, P.P. Brons, B.A.P. Laros‐van Gorkom, W.L. van Heerde, F. Leebeek, M. Kruip, M.H. Cnossen, E. Mauser‐Bunschoten, K. Fischer, F.J. Smiers, C. Hermans, R. Klamroth, C. Escuriola‐Ettingshausen, C. Königs, P. Petrini, M. Holmström, A. Mäkipernaa, C. Male, I. Pabinger, R.D. Keenan, R. Liesner, K. Khair, T.T. Yee, D.P. Hart, S. Rangarajan, M. Mitchell, G. Thompson, S. Haya, A. Moret, A.R. Cid, V. Jimenez‐Yuste, M.E. Mancuso, M.G. Mazzuconni, C. Santoro, M. Morfini, G. Castaman, P. Schinco, G.F. Rivolta, H. Platokouki, S. McRae
Publikováno v:
Journal of Thrombosis and Haemostasis, 13(7), 1217-1225. Wiley
Journal of Thrombosis and Haemostasis, 13(7), 1217-1225
Journal of thrombosis and haemostasis, 13(7), 1217-1225. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13, 1217-25
Journal of Thrombosis and Haemostasis, 13, 7, pp. 1217-25
Journal of Thrombosis and Haemostasis, 13(7), 1217. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13(7), 1217-1225
Journal of thrombosis and haemostasis, 13(7), 1217-1225. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13, 1217-25
Journal of Thrombosis and Haemostasis, 13, 7, pp. 1217-25
Journal of Thrombosis and Haemostasis, 13(7), 1217. Wiley-Blackwell
BACKGROUND: The life expectancy of non-severe hemophilia A (HA) patients equals the life expectancy of the non-hemophilic population. However, data on the effect of inhibitor development on mortality and on hemophilia-related causes of death are scar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d5b169bde53c72df8027f9087821d9f
https://research.rug.nl/en/publications/1e934363-fdf0-4dda-a41c-959edc3a8469
https://research.rug.nl/en/publications/1e934363-fdf0-4dda-a41c-959edc3a8469
Autor:
E., De Wee, M., Knol, E., Mauser-Bunschoten, A., Van Der Bom, M., Degenaar-Dujardin, J.C.J., Eikenboom, K., Fijnvandraat, A., De Goede-Bolder, B., Laros-Van Gorkom, P., Ypma, S., Zweegman, K., Meijer
Publikováno v:
Blood, 116(21). American Society of Hematology
E., D W, M., K, E., M-B, A., V D B, M., D-D, J.C.J., E, K., F, A., D G-B, B., L-V G, P., Y, S., Z & K., M 2010, ' Women with moderate and severe Von Willebrand disease have a high morbidity of gynecological and obstetric bleeding ', Blood, vol. 116, no. 21 . < http://abstracts.hematologylibrary.org/cgi/content/abstract/116/21/542?maxtoshow=&hits=60&RESULTFORMAT=&searchid=1&FIRSTINDEX=780&displaysectionid=Oral+Session&fdate=1/1/2010&tdate=12/31/2010&resourcetype=HWCIT http://ovidsp.ovid.com/ovidweb.cgi?T=JS&PAGE >
E., D W, M., K, E., M-B, A., V D B, M., D-D, J.C.J., E, K., F, A., D G-B, B., L-V G, P., Y, S., Z & K., M 2010, ' Women with moderate and severe Von Willebrand disease have a high morbidity of gynecological and obstetric bleeding ', Blood, vol. 116, no. 21 . < http://abstracts.hematologylibrary.org/cgi/content/abstract/116/21/542?maxtoshow=&hits=60&RESULTFORMAT=&searchid=1&FIRSTINDEX=780&displaysectionid=Oral+Session&fdate=1/1/2010&tdate=12/31/2010&resourcetype=HWCIT http://ovidsp.ovid.com/ovidweb.cgi?T=JS&PAGE >
Introduction: Von Willebrand Disease (VWD) is the most common inherited bleeding disorder worldwide. Men and women are equally likely to be affected, but in women VWD is more often clinically manifest because of bleeding associated with menstruation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::aaa311b6c8ac5a0bb7e8a58e8c91445b
https://research.vumc.nl/en/publications/d55f1e98-2904-4248-9a6c-5b675d1635d4
https://research.vumc.nl/en/publications/d55f1e98-2904-4248-9a6c-5b675d1635d4
Publikováno v:
Vox sanguinis. 75(4)
In order to describe the progression of HIV disease in a cohort of Dutch HIV-1-infected patients with haemophilia and to study the influence of clinical and clotting factors, we performed a 15-year longitudinal clinical and laboratory study.The progr
Autor:
Y, Sawamoto, R, Prescott, D, Zhong, E L, Saenko, E, Mauser-Bunschoten, K, Peerlinck, M, van den Berg, D, Scandella
Publikováno v:
Thrombosis and haemostasis. 79(1)
From June, 1990, to November, 1991, in The Netherlands and Belgium, 16 previously treated severe hemophilia A patients (PTP) developed inhibitors after exposure to factor VIII CPS-P, a new heat pasteurized product. A previously untreated patient (PUP
Publikováno v:
Blood. 88(9)
Hemophilia B is a bleeding disorder caused by a deficiency of clotting factor IX (FIX). A colony of FIX deficient Lhasa Apso dogs has been established and the molecular basis of hemophilia B has been determined. The plasma factor IX levels were1% of
Autor:
E, Mauser, N A, Miller
Publikováno v:
Health Care Financing Review
Recently, the use of home health services by Medicare beneficiaries has been growing. From 1987 to 1992, the percentage of all enrollees receiving home health rose from 4.8 to 7.2 percent, while the average number of visits among users increased from
Publikováno v:
Thrombosis and haemostasis. 73(2)
Antibodies against factor VIII coagulant activity can appear in haemophiliacs who are treated with factor VIII preparations but also spontaneously in non-haemophiliacs. The Bethesda assay is the most commonly used method to detect these antibodies, b
Publikováno v:
The Journal of Immunology. 116:747-754
Mast cells were differentiated by long-term culture of rat thymus cells on rat embryonic fibroblast monolayers. Mature mast cells obtained in the culture were morphologically similar to normal peritoneal and thoracic mast cells and possessed specific
Autor:
James E. Mauser
Publikováno v:
Metallurgical Transactions B. 13:511-513
Volatilization of secondary metals such as arsenic, antimony, and bismuth, during the smelting of copper ores, is important because of environmental and resource considerations. The Bureau of Mines, United States Department of the Interior, has been