Zobrazeno 1 - 10
of 239
pro vyhledávání: '"K. Hamulyak"'
Publikováno v:
European Journal of Haematology, 59, 2, pp. 105-109
European Journal of Haematology, 59, 105-109
European Journal of Haematology, 59, 105-109
The present study reports on the treatment of bleeding episodes and the natural history of factor VIII inhibitors in 4 patients with acquired haemophilia A postpartum. Low titre type II factor VIII inhibitors in 3 patients and high titre type I inhib
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
Publikováno v:
Phlebologie, 32, 45-49. Georg Thieme Verlag
SummaryAim: Evaluation of the use of compression therapy in the management of deep venous thrombosis. Methods: Postal questionnaire among all dermatologists in the Netherlands. Results: The overall response rate was 81%. Availability of a treatment p
Autor:
S. P. Kaandorp, M. Goddijn, J. A. M. Post van der, B. A. Hutten, H. R. Verhoeve, K. Hamulyak, B. W. Mol, N. Folkeringa, M. Nahuis, D. N. M. Papatsonis, H. R. Buller, F. Veen van der, S. Middeldorp, B. N. Chakravarty, P. Chakraborty, S. Sharma, A. Mondal, S. N. Kabir, S. Bhattacharya, E. R. Love, N. C. Smith, Y. E. M. Koot, C. B. Boomsma, M. C. J. Eijkemans, E. G. Lentjes, N. S. Macklon, V. Rittenberg, S. Sobaleva, A. Al-Hadi, Y. Khalaf, P. Braude, T. El-Toukhy
Publikováno v:
Human Reproduction. 25:i28-i30
Publikováno v:
Thrombosis and Haemostasis. 74:580-583
SummaryWe recently reported a high prevalence of the FV Leiden mutation (R506Q, responsible for Activated Protein C resistance) among symptomatic protein C deficient probands (19%), and the involvement of the FV Leiden mutation in the expression of t
Autor:
M D, Lancé, M, Ninivaggi, S E M, Schols, M A H, Feijge, S K, Oehrl, G J A J M, Kuiper, M, Nikiforou, M A E, Marcus, K, Hamulyak, E C M, van Pampus, H, ten Cate, J W M, Heemskerk
Publikováno v:
Vox sanguinis. 103(1)
Treatment of dilutional coagulopathy by transfusing fresh frozen plasma (FFP) remains sub-optimal. We hypothesized that partial replacement of transfused FFP by fibrinogen concentrate results in improved coagulant activity and haemostasis. This was t
Publikováno v:
Acta Dermato-Venereologica. 82:52-54
We present a young male patient referred to our hospital with leg ulcers on both legs that were more than 3 years refractory to standard treatment with compression therapy. By thrombophilia screening factor V Leiden mutation, hyperhomocysteinemia and
Publikováno v:
Vasa. Journal of Vascular Diseases, 33, 19-24. Hogrefe Publishing
Background: Impaired microcirculation in chronic venous insufficiency leads to chronic inflammation and dystrophic changes of the skin, and finally to leg ulceration. The purpose of this study was to investigate in more detail coagulation and fibrino
Publikováno v:
Thrombosis and haemostasis. 84(4)
In von Willebrand disease (vWD) type 1 and mild haemophilia A patients we studied the effect of an infusion of DDAVP (0.3 microg/kg body weight) on thrombin generation in platelet-rich plasma (PRP) and platelet-poor plasma (PPP). Baseline thrombin ge