Zobrazeno 1 - 10
of 217
pro vyhledávání: '"J. Voorberg"'
Autor:
A. Abdi, M. R. Bordbar, S. Hassan, F. R. Rosendaal, J. G. van der Bom, J. Voorberg, K. Fijnvandraat, S. C. Gouw
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Objectives: In hemophilia A the presence of non-neutralizing antibodies (NNAs) against Factor VIII (FVIII) may predict the development of neutralizing antibodies (inhibitors) and accelerate the clearance of administrated FVIII concentrates. This syst
Externí odkaz:
https://doaj.org/article/bc4e38a9c0724061ab28a8543f7fff23
Autor:
M Miranda, E Brandsma, P Kaijen, F Van Alphen, R Van Bruggen, K Fijnvandraat, S Lacroix-Desmazes, J Voorberg
Publikováno v:
GTH Congress 2023 – 67th Annual Meeting of the Society of Thrombosis and Haemostasis Research – The patient as a benchmark.
Autor:
J. Voorberg, Xiaoke Pan, P.L. Hordijk, Petr Symersky, Olga Tura-Ceide, J. Majolee, Robert Szulcek, Herman J Bogaard, X. D. Manz
Publikováno v:
American Journal of Respiratory and Critical Care Medicine, 201. American Thoracic Society
Manz, X D, Pan, X, Symersky, P, Majolee, J, Tura-Ceide, O, Hordijk, P L, Voorberg, J, Bogaard, H J & Szulcek, R 2020, ' The Activated Pulmonary Endothelium of Chronic Thromboembolic Pulmonary Hypertension Patients Exhibits Elevated Platelet Adhesion ', American Journal of Respiratory and Critical Care Medicine, vol. 201 .
Manz, X D, Pan, X, Symersky, P, Majolee, J, Tura-Ceide, O, Hordijk, P L, Voorberg, J, Bogaard, H J & Szulcek, R 2020, ' The Activated Pulmonary Endothelium of Chronic Thromboembolic Pulmonary Hypertension Patients Exhibits Elevated Platelet Adhesion ', American Journal of Respiratory and Critical Care Medicine, vol. 201 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a617839f44c3c6e28c0efe6175d48e2
https://research.vumc.nl/en/publications/5c8b33d3-ea28-4046-8983-697c8e8f338d
https://research.vumc.nl/en/publications/5c8b33d3-ea28-4046-8983-697c8e8f338d
Publikováno v:
HemaSphere. 3:354-355
Autor:
C. M. C. Bank, Ellen A. M. Turenhout, J. Voorberg, E. N. Van Den Brink, S. M. H. Timmermans, Karin Fijnvandraat, M. Peters
Publikováno v:
Thrombosis and Haemostasis. 81:723-726
SummaryRecent studies suggest that certain missense mutations associated with mild to moderate haemophilia A predispose to inhibitor development. In this study, we present a longitudinal analysis of the epitope specificity of an inhibitor that develo
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(102)
Development of inhibitory antibodies to factor VIII (FVIII) provides a major complication of replacement therapy in patients with haemophilia A. The risk of inhibitor formation is influenced by the underlying FVIII gene defect. Moreover, genetic dete
Autor:
P M W, van Helden, P H P, Kaijen, E P, Mauser-Bunschoten, K, Fischer, H M, van den Berg, J, Voorberg
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(6)
Frequent administration of high dosages factor VIII (FVIII), so-called immune tolerance induction (ITI), provides an efficient strategy to eradicate inhibitory antibodies in patients with haemophilia A. At present, our knowledge on the characteristic
Publikováno v:
Journal of thrombosis and haemostasis, 5(11), 2306-2308. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 5(11), 2306-2308. Wiley
Journal of Thrombosis and Haemostasis, 5(11), 2306-2308. Wiley
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77400f08e58a000d216e4538454cdc64
https://pure.amc.nl/en/publications/factor-viiispecific-memory-b-cells-in-patients-with-hemophilia-a(77367654-c1cf-4692-afc6-98822804484e).html
https://pure.amc.nl/en/publications/factor-viiispecific-memory-b-cells-in-patients-with-hemophilia-a(77367654-c1cf-4692-afc6-98822804484e).html
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 9(5)
The inhibitory capacity of plasma samples from 24 patients with severe haemophilia A and high-responding inhibitors were evaluated in a concentrate-based assay using two plasma-derived (Haemate and Monoclate-P) and three recombinant (Helixate, Recomb
Autor:
E N, van den Brink, E A, Turenhout, E C, Wijn-Maas, F J, van der Meer, J, Voorberg, L J, Bosch
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 6(6)
We describe a previously healthy woman who at the age of 44 years developed a factor VIII inhibitor, that over the years increased to a maximum level of 3600 Bethesda units (BU) mL(-1) in 1978. The epitope specificity of the factor VIII inhibitor was