Zobrazeno 1 - 10
of 188
pro vyhledávání: '"E.P. Mauser‐Bunschoten"'
Akademický článek
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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:
Y.V. Sanders, J.G. van der Bom, A. Isaacs, M.H. Cnossen, M.P.M. de Maat, B.A.P. Laros-van Gorkom, K. Fijnvandraat, K. Meijer, C.M. van Duijn, E.P. Mauser-Bunschoten, J. Eikenboom, F.W.G. Leebeek, M. Coppens, A. Kors, J. de Meris, M.R. Nijziel, R.Y.J. Tamminga, P.F. Ypma, F.J.W. Smiers, B. Granzen, K. Hamulyák, P. Brons
Publikováno v:
Journal of Thrombosis and Haemostasis, 13(6), 956-966
Journal of Thrombosis and Haemostasis, 13, 956-66
Journal of Thrombosis and Haemostasis, 13, 6, pp. 956-66
Journal of Thrombosis and Haemostasis, 13(6), 956. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13(6), 956-66. Wiley
Journal of Thrombosis and Haemostasis, 13(6), 956-966. Wiley-Blackwell Publishing Ltd
Journal of thrombosis and haemostasis, 13(6), 956-966. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13(6), 956-966. Wiley
Journal of Thrombosis and Haemostasis, 13, 956-66
Journal of Thrombosis and Haemostasis, 13, 6, pp. 956-66
Journal of Thrombosis and Haemostasis, 13(6), 956. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13(6), 956-66. Wiley
Journal of Thrombosis and Haemostasis, 13(6), 956-966. Wiley-Blackwell Publishing Ltd
Journal of thrombosis and haemostasis, 13(6), 956-966. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13(6), 956-966. Wiley
Item does not contain fulltext BACKGROUND: von Willebrand factor (VWF) levels in healthy individuals are influenced by variations in genetic loci other than the VWF gene, whose contribution to VWF levels in patients with von Willebrand disease (VWD)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c458bd0d32df3fb65621182fdb532fa2
http://hdl.handle.net/1887/102139
http://hdl.handle.net/1887/102139
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
K.P., Van Galen, Y.V., Sanders, U., Vojinovic, J., Eikenboom, M.H., Cnossen, S., Zweegman, R.E., Schutgens, A.G., Van Der Bom, K., Fijnvandraat, B., Laros-Van Gorkom, K., Meijer, M.R., Nijziel, F., Leebeek, E.P., Mauser-Bunschoten
Publikováno v:
K.P., V G, Y.V., S, U., V, J., E, M.H., C, S., Z, R.E., S, A.G., V D B, K., F, B., L-V G, K., M, M.R., N, F., L & E.P., M-B 2014, ' The occurrence and impact of joint bleeds in Von Willebrand disease ', Haematologica, vol. 99, pp. 232 . < http://www.embase.com/search/results?subaction=viewrecord&from=export&id=L71700146 http://www.haematologica.org/content/99/supplement_1/1.full.pdf+html LK-http://sfx.library.uu.nl/utrecht?sid=EMBASE&issn=03906078&id=doi:&atitle=The+occurrence+and+impac >
Haematologica, 99. Ferrata Storti Foundation
Haematologica, 99. Ferrata Storti Foundation
Background: Von Willebrand disease (VWD) is a heterogeneous inherited bleeding disorder that affects up to 1% of the population. Joint bleeds are not predominant, but have been reported to occur in 8-45% of patients with VWD, especially in those with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::fb1837c601cb7a3851084d8f8e5f4763
https://research.vumc.nl/en/publications/3e1f165f-6fcc-4798-99cc-d5c0f29cc8af
https://research.vumc.nl/en/publications/3e1f165f-6fcc-4798-99cc-d5c0f29cc8af
Autor:
K., Van Galen, Y.V., Sanders, U., Vojinovic, J.C., Eikenboom, M.H., Cnossen, S., Zweegman, J.G., Van Der Bom, C.J., Fijnvandraat, B., Laros-Van Gorkom, K., Meijer, E.P., Mauser-Bunschoten, F., Leebeek
Publikováno v:
Haemophilia, 20, 50-51. Wiley-Blackwell Publishing Ltd
K., V G, Y.V., S, U., V, J.C., E, M.H., C, S., Z, J.G., V D B, C.J., F, B., L-V G, K., M, E.P., M-B & F., L 2014, ' Consequences of joint bleeds in von Willebrand disease patients: A retrospective patient control study ', Haemophilia, vol. 20, pp. 50-51 . https://doi.org/10.1111/hae.12353 LK-http://resolver.ebscohost.com/openurl?sid=EMBASE&issn=13518216&id=doi:10.1111%2Fhae.12353&atitle=Consequences+of+joint+bleeds+in+von+Willebrand+disease+patients%3A+A+retrospective+patient+control+study&stitle=Haemophilia&title=Haemophilia&volume=20&issue=&spage=50&epage=51&aulast=Van+Galen&aufirst=K.&auinit=K.&aufull=Van+Galen+K.&coden=&isbn=&pages=50-51&date=2014&auinit1=K&auinitm=
K., V G, Y.V., S, U., V, J.C., E, M.H., C, S., Z, J.G., V D B, C.J., F, B., L-V G, K., M, E.P., M-B & F., L 2014, ' Consequences of joint bleeds in von Willebrand disease patients: A retrospective patient control study ', Haemophilia, vol. 20, pp. 50-51 . https://doi.org/10.1111/hae.12353 LK-http://resolver.ebscohost.com/openurl?sid=EMBASE&issn=13518216&id=doi:10.1111%2Fhae.12353&atitle=Consequences+of+joint+bleeds+in+von+Willebrand+disease+patients%3A+A+retrospective+patient+control+study&stitle=Haemophilia&title=Haemophilia&volume=20&issue=&spage=50&epage=51&aulast=Van+Galen&aufirst=K.&auinit=K.&aufull=Van+Galen+K.&coden=&isbn=&pages=50-51&date=2014&auinit1=K&auinitm=
Introduction: Joint bleeds (JB) have been reported to occur in 8-45% of von Willebrand disease (VWD) patients, depending on VWD severity. The consequences of JB in VWD are largely unknown. Therefore, we started a patient control study based on retros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5f98bae5ac8f1bb4844934a89c58fd43
https://research.vumc.nl/en/publications/8bd4ef2d-90f1-4984-a57c-f9d66f5a8eae
https://research.vumc.nl/en/publications/8bd4ef2d-90f1-4984-a57c-f9d66f5a8eae
Autor:
E.P. Mauser‐Bunschoten
Publikováno v:
Inhibitors in Patients with Haemophilia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::546f57e755d02bc2d4da006db8d586f8
https://doi.org/10.1002/9780470757260.ch8
https://doi.org/10.1002/9780470757260.ch8
Autor:
E.P. Mauser-Bunschoten
Publikováno v:
Annals of the Rheumatic Diseases. 74:49.2-49
Introduction Haemophilia is an X linked inherited disease characterised by a deficiency in factor VIII (haemophilia A) or IX (haemophilia B) leading to impaired secondary haemostasis. Bleeds are mainly located into the synovial joints especially knee
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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