Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Paul P T, Brons"'
Autor:
Annet Simons, Paul P. T. Brons, Frank W.G. Leebeek, Daniëlle Meijer, Selene C M Schoormans, Britta A P Laros-van Gorkom, Waander L. van Heerde, Sandy Krouwel, Laurens Nieuwenhuizen, Dominique P M S M Maas, Nicole M. A. Blijlevens, Saskia E M Schols, Ferdows Atiq
Publikováno v:
Journal of Thrombosis and Haemostasis, 20(2), 316-327. Wiley-Blackwell Publishing Ltd
Journal of Thrombosis and Haemostasis, 20, 2, pp. 316-327
Journal of Thrombosis and Haemostasis, 20, 316-327
Journal of Thrombosis and Haemostasis, 20, 2, pp. 316-327
Journal of Thrombosis and Haemostasis, 20, 316-327
Contains fulltext : 248232.pdf (Publisher’s version ) (Open Access) BACKGROUND: An appropriate clinical diagnosis of von Willebrand disease (VWD) can be challenging because of a variable bleeding pattern and laboratory phenotype. Genotyping is a po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69cc08c282316528b8364c12e641bfea
https://pure.eur.nl/en/publications/ddb294bc-b7d6-4300-b9b9-372b6bb0b800
https://pure.eur.nl/en/publications/ddb294bc-b7d6-4300-b9b9-372b6bb0b800
Autor:
Nicole M. A. Blijlevens, M.R. Nijziel, Joline L Saes, Bert A. van der Reijden, Waander L. van Heerde, Y. Smit, Paul P. T. Brons, Annet Simons, Sonja A. de Munnik, Saskia E M Schols, Marjolijn C.J. Jongmans
Publikováno v:
Haemophilia, 25, 127-135
Haemophilia, 25, 1, pp. 127-135
Haemophilia, 25(1), 127. Wiley-Blackwell
Haemophilia, 25, 1, pp. 127-135
Haemophilia, 25(1), 127. Wiley-Blackwell
INTRODUCTION: Bleeding assessment tools and laboratory phenotyping often remain inconclusive in patients with a haemorrhagic diathesis. AIM: To describe the phenotype and genetic profile of patients with a bleeding tendency. METHODS: Whole exome sequ
Autor:
E.J. van Beers, C. Ootjers, Sanne M. Meinderts, Paul P. T. Brons, H. Heijboer, Ilja Oomen, C. E. Van Der Schoot, F. G. Hofstede, Saskia E M Schols, L. Dovern, Sonja A.M.C. Teuben, I. van Vliet, Bart J. Biemond, Erfan Nur, Jorn J. Gerritsma, M. Beijlevelt, M.H. Suiker, Jean-Louis H. Kerkhoffs, Karin Fijnvandraat, E. Zwagemaker, Anita W. Rijneveld, C. F. J. van Tuijn, Marjon H. Cnossen, Frans J. Smiers, J. G. van der Bom, P.J. de Pagter
Publikováno v:
Blood Reviews. 48:100794
Red blood cell (RBC) alloimmunization is a serious complication of blood transfusions, challenging selection of compatible units for future transfusions. Genetic characteristics may be associated with the risk of RBC alloimmunization and may therefor
Autor:
Eveline S. J. M. de Bont, Marina Borisevich, Birgitte Lausen, Paul P. T. Brons, Clara M. A. de Bruijn, Meinolf Suttorp, Frédéric Millot
Publikováno v:
British Journal of Haematology, 185(4), 718-724. Wiley
British Journal of Haematology, 185, 718-724
British Journal of Haematology, 185, 4, pp. 718-724
British Journal of Haematology, 185, 718-724
British Journal of Haematology, 185, 4, pp. 718-724
This international study aimed to assess the effect of imatinib discontinuation in paediatric patients with chronic myeloid leukaemia (CML) after deep molecular remission (DMR) had been achieved and maintained for at least 2 years. The primary endpoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bda3b9e8e111c52a0b5fbe54d7d0b14
https://research.rug.nl/en/publications/c9caca65-6f6f-4366-a8b7-8ce8f379e5b5
https://research.rug.nl/en/publications/c9caca65-6f6f-4366-a8b7-8ce8f379e5b5
Autor:
Andre J Vlot, Martine Raphael, L Thom Vlasveld, Tessa M. A. Peters, A. Birgitta Versluijs, Alexander J. Rennings, Dorine W. Swinkels, Bert van den Heuvel, Mirian C. H. Janssen, Frank L. van de Veerdonk, Michel van Gelder, Dirk L Bakkeren, Charlotte C.M. Schaap, Bernd Granzen, Anita W. Rijneveld, Paul P. T. Brons, V.M.J. Novotny, Albertine E. Donker, Inge M. Appel, R.J.H. Smeets, M.R. Nijziel
Publikováno v:
American Journal of Hematology, 91, E482-e490
Donker, A E, Schaap, C C M, Novotny, V M J, Smeets, R, Peters, T M A, van den Heuvel, B L P, Raphael, M F, Rijneveld, A W, Appel, I M, Vlot, A J, Versluijs, A B, van Gelder, M, Granzen, B, Janssen, M C H, Rennings, A J M, van de Veerdonk, F L, Brons, P P T, Bakkeren, D L, Nijziel, M R, Vlasveld, L T & Swinkels, D W 2016, ' Iron refractory iron deficiency anemia : a heterogeneous disease that is not always iron refractory ', American Journal of Hematology, vol. 91, no. 12, pp. E482-E490 . https://doi.org/10.1002/ajh.24561
American Journal of Hematology, 91(12), E482-E490. Wiley-Liss Inc.
American Journal of Hematology, 91(12), E482-E490. Wiley
American Journal of Hematology, 91, 12, pp. E482-e490
American Journal of Hematology, 91(12), E482. Wiley-Liss Inc.
American Journal of Hematology
Donker, A E, Schaap, C C M, Novotny, V M J, Smeets, R, Peters, T M A, van den Heuvel, B L P, Raphael, M F, Rijneveld, A W, Appel, I M, Vlot, A J, Versluijs, A B, van Gelder, M, Granzen, B, Janssen, M C H, Rennings, A J M, van de Veerdonk, F L, Brons, P P T, Bakkeren, D L, Nijziel, M R, Vlasveld, L T & Swinkels, D W 2016, ' Iron refractory iron deficiency anemia : a heterogeneous disease that is not always iron refractory ', American Journal of Hematology, vol. 91, no. 12, pp. E482-E490 . https://doi.org/10.1002/ajh.24561
American Journal of Hematology, 91(12), E482-E490. Wiley-Liss Inc.
American Journal of Hematology, 91(12), E482-E490. Wiley
American Journal of Hematology, 91, 12, pp. E482-e490
American Journal of Hematology, 91(12), E482. Wiley-Liss Inc.
American Journal of Hematology
Contains fulltext : 172863.pdf (Publisher’s version ) (Open Access) TMPRSS6 variants that affect protein function result in impaired matriptase-2 function and consequently uninhibited hepcidin production, leading to iron refractory iron deficiency
Autor:
Rienk Y. J. Tamminga, Johanna G. van der Bom, Joke de Meris, Y V Sanders, Johan Boender, Paul P. T. Brons, Marjon H. Cnossen, Karin Fijnvandraat, Frans J. Smiers, Frank W.G. Leebeek, Evelien P. Mauser-Bunschoten, Bernd Granzen
Publikováno v:
American Journal of Hematology. 90:1142-1148
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in detail to facilitate diagnosis during childhood and aid in the planning and assessment of treatment strategies. The objective was to evaluate the occurr
Autor:
Natasja Dors, Paul P. T. Brons, J. G. van der Bom, Anne Mäkipernaa, Saturnino Haya, M. Peters, Jan Voorberg, A S van Velzen, M. Holmström, Corien L. Eckhardt, Karin Fijnvandraat, Janneke I. Loomans
Publikováno v:
Journal of Thrombosis and Haemostasis, 15, 246-254
Journal of Thrombosis and Haemostasis, 15(2), 246-254
Journal of thrombosis and haemostasis : JTH
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Journal of thrombosis and haemostasis, 15(2), 246-254. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 15, 2, pp. 246-254
Journal of Thrombosis and Haemostasis, 15(2), 246-254
Journal of thrombosis and haemostasis : JTH
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Journal of thrombosis and haemostasis, 15(2), 246-254. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 15, 2, pp. 246-254
Contains fulltext : 170609.pdf (Publisher’s version ) (Closed access) Essentials Factor VIII levels vary in mild and moderate hemophilia A (MHA) patients with the same mutation. We aimed to estimate the variation and determinants of factor VIII lev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d4c2189f4edbfae1214b417bc106651
https://doi.org/10.1111/jth.13581
https://doi.org/10.1111/jth.13581
Autor:
E E Deurloo, C. van den Bos, Willeke A. M. Blokx, L J F Janssen, Paul P. T. Brons, H.W.B. Schreuder
Publikováno v:
British Journal of Dermatology, 176, e33-e33
British Journal of Dermatology, 176, 4, pp. e33-e33
British journal of dermatology, 176(4). Wiley-Blackwell
British Journal of Dermatology, 176, 4, pp. e33-e33
British journal of dermatology, 176(4). Wiley-Blackwell
Contains fulltext : 174004.pdf (Publisher’s version ) (Closed access) 01 april 2017
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9760ad789c637422df052b6095d65adb
http://hdl.handle.net/2066/174004
http://hdl.handle.net/2066/174004
Autor:
Nina Streefkerk, Waander L. van Heerde, Berthold S. Iegmund, Thynn Thynn Yee, Ril Iesner, Elena Santagostino, Pieter Willem Kamphuisen, Eveline P. Mauser-Bunschoten, Carmen Escuriola-Ettingshausen, Paul P. T. Brons, Victor J. Imenez-Yuste, Daniel P. Hart, Corien L. Eckhardt, Maria Gabriella Mazzucconi, Kathelijne Peerlinck, Annarita Tagliaferri, Savita Rangarajan, Christoph Male, S Imon Mcrae, Natasja Dors, Marjolein Peters, P. Iercarla Schinco, Frans J. Smiers, Giancarlo Castaman, Karin Fijnvandraat, Helen Platokouki, M. Holmström, Russell Keenan, Johanna G. van der Bom, Britta A P Laros-van Gorkom, Marjon H. Cnossen, Frank W.G. Leebeek, Johannes Oldenburg, Charles R. M. Hay, Robert Klamroth, Anne Mäkipernaa, Cédric Hermans, Pia Petrini, Karly Hamulyák, Sylvia Reitter-Pfoertner, Saturnino Haya, Karina Meijer, Massimo Morfini, Alice S. van Velzen, M.R. Nijziel, Jan Astermark
Publikováno v:
Haemophilia. 20:1-186
Introduction and Objectives: Neutralizing antibodies (inhibitors) directed against the FVIII protein may increase the bleeding frequency and compromise the management of bleeding episodes in nonsevere haemophilia A patients. The median annual bleedin
Autor:
Anne Kruempel, M. David, Mary Morgan, Paul P. T. Brons, Paul Monagle, Karin Kurnik, Ulrike Nowak-Göttl, Martin Olivieri, Hans-Joerg Hertfelder, Mary Mathias, Adrian Minford, Antonio Molines Honrubia, Wolfgang Behnisch, Natividad Gomez Gomez
Publikováno v:
British Journal of Haematology. 164:414-421
Since the first description of subcutaneous protein C concentrate as treatment for severe protein C deficiency in 1996, further cases have been reported but there is no uniform approach to this form of treatment. In order to assess the safety and eff