Zobrazeno 1 - 10
of 82
pro vyhledávání: '"R. Kloosterman"'
Autor:
Anne‐Fleur Zwagemaker, Fabienne R. Kloosterman, Michiel Coppens, Samantha C. Gouw, Sara Boyce, Catherine N. Bagot, Erik A. M. Beckers, Paul Brons, Giancarlo Castaman, Jeroen Eikenboom, Shannon Jackson, Marieke J. H. A. Kruip, Frank W. G. Leebeek, Karina Meijer, Laurens Nieuwenhuizen, Ingrid Pabinger, Karin Fijnvandraat, the DYNAMO Study Group
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 6, Iss 6, Pp n/a-n/a (2022)
Abstract Background Desmopressin is an important treatment option in nonsevere hemophilia A because it has several benefits compared with factor (F) concentrates, including no inhibitor risk and much lower costs. Despite these advantages, data are li
Externí odkaz:
https://doaj.org/article/a16e8de542a44393ab495934c494f90e
Autor:
Fabienne R. Kloosterman, Anne-Fleur Zwagemaker, Anne C. Bay-Jensen, Marjon H. Cnossen, Marieke J.H.A. Kruip, Frank W.G. Leebeek, Robert Hemke, Mario Maas, Karin Fijnvandraat, Samantha C. Gouw, Michiel Coppens
Publikováno v:
Journal of Thrombosis and Haemostasis. Wiley-Blackwell
Kloosterman, F R, Zwagemaker, A-F, Bay-Jensen, A C, Cnossen, M H, Kruip, M J H A, Leebeek, F W G, Hemke, R, Maas, M, Fijnvandraat, K, Gouw, S C & Coppens, M 2023, ' Poor correlation between biomarkers and MRI-detected joint damage in a cross-sectional study of persons with nonsevere hemophilia A (DYNAMO study) ', Journal of Thrombosis and Haemostasis, vol. 21, no. 7, pp. 1813-1823 . https://doi.org/10.1016/j.jtha.2023.03.030
Kloosterman, F R, Zwagemaker, A-F, Bay-Jensen, A C, Cnossen, M H, Kruip, M J H A, Leebeek, F W G, Hemke, R, Maas, M, Fijnvandraat, K, Gouw, S C & Coppens, M 2023, ' Poor correlation between biomarkers and MRI-detected joint damage in a cross-sectional study of persons with nonsevere hemophilia A (DYNAMO study) ', Journal of Thrombosis and Haemostasis, vol. 21, no. 7, pp. 1813-1823 . https://doi.org/10.1016/j.jtha.2023.03.030
Background: Persons with nonsevere hemophilia A (NSHA) experience less frequent joint bleeding than persons with severe hemophilia A, but may still develop joint damage. Biomarkers of cartilage and synovial remodeling can reflect ongoing pathologic p
Autor:
Fabienne R. Kloosterman, Anne-Fleur Zwagemaker, Catherine N. Bagot, Erik A. M. Beckers, Giancarlo Castaman, Marjon H. Cnossen, Peter W. Collins, Charles Hay, Michel Hof, Britta Laros-van Gorkom, Frank W. G. Leebeek, Christoph Male, Karina Meijer, Ingrid Pabinger, Susan Shapiro, Michiel Coppens, Karin Fijnvandraat, Samantha C. Gouw
Publikováno v:
Blood, 6(14), 4256-4265. American Society of Hematology
Blood Advances, 6, 14, pp. 4256-4265
the DYNAMO Study Group 2022, ' The bleeding phenotype in people with nonsevere hemophilia ', Blood, vol. 6, no. 14, pp. 4256-4265 . https://doi.org/10.1182/bloodadvances.2022007620
Blood advances, 6(14), 4256-4265. American Society of Hematology
Blood Advances, 6, 4256-4265
Blood Advances, 6(14), 4256-4265. AMER SOC HEMATOLOGY
Blood advances, 6(14), 4256-4265. The American Society of Hematology
Blood Advances, 6, 14, pp. 4256-4265
the DYNAMO Study Group 2022, ' The bleeding phenotype in people with nonsevere hemophilia ', Blood, vol. 6, no. 14, pp. 4256-4265 . https://doi.org/10.1182/bloodadvances.2022007620
Blood advances, 6(14), 4256-4265. American Society of Hematology
Blood Advances, 6, 4256-4265
Blood Advances, 6(14), 4256-4265. AMER SOC HEMATOLOGY
Blood advances, 6(14), 4256-4265. The American Society of Hematology
Detailed information on the onset, frequency, and severity of bleeding in nonsevere hemophilia is limited. We aimed to assess the bleeding phenotype of persons with nonsevere hemophilia and to analyze the association between baseline factor VIII/IX (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::693d1d6e7e955cbedf53b0b23b5e64b0
https://research.vumc.nl/en/publications/a277ee53-2884-4efb-b02c-1a33799e92ea
https://research.vumc.nl/en/publications/a277ee53-2884-4efb-b02c-1a33799e92ea
Akademický článek
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Autor:
Anne‐Fleur Zwagemaker, Fabienne R. Kloosterman, Robert Hemke, Samantha C. Gouw, Michiel Coppens, Lorenzo G.R. Romano, Marieke J.H.A. Kruip, Marjon H. Cnossen, Frank W.G. Leebeek, Barbara A. Hutten, Mario Maas, Karin Fijnvandraat
Publikováno v:
Journal of Thrombosis and Haemostasis, 20(5), 1126-1137. Wiley-Blackwell Publishing Ltd
Journal of thrombosis and haemostasis, 20(5), 1126-1137. Wiley-Blackwell
Journal of thrombosis and haemostasis, 20(5), 1126-1137. Wiley-Blackwell
Background: Joint bleeding in hemophilia may eventually lead to joint damage. In nonsevere hemophilia, joint bleeds occur infrequently. Currently, knowledge on the joint status of patients with nonsevere hemophilia using objective imaging is limited.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa49c80c1efcc094b4f66f596326b2c9
https://pure.eur.nl/en/publications/0641bf84-f975-4e1f-8172-86ef4c119161
https://pure.eur.nl/en/publications/0641bf84-f975-4e1f-8172-86ef4c119161
Publikováno v:
Journal of thrombosis and haemostasis, 19(10), 2642-2644. Wiley-Blackwell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::472b84e069b6706aab7ac30b1b8653ba
https://pure.amc.nl/en/publications/the-factor-viii-treatment-history-of-nonsevere-hemophilia-aresponse-from-original-authors-abdi-et-al(11a9bfcd-5043-4c8b-9ba8-b1040e404552).html
https://pure.amc.nl/en/publications/the-factor-viii-treatment-history-of-nonsevere-hemophilia-aresponse-from-original-authors-abdi-et-al(11a9bfcd-5043-4c8b-9ba8-b1040e404552).html
Publikováno v:
Pain Medicine, 21, 201-203
Pain Medicine, 21, 1, pp. 201-203
Pain Medicine, 21, 1, pp. 201-203
Contains fulltext : 221572.pdf (Publisher’s version ) (Closed access)
Akademický článek
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Akademický článek
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Autor:
Fabienne R. Kloosterman, Anne-Fleur Zwagemaker, Giancarlo Castaman, Karin Fijnvandraat, Samantha C. Gouw, Amal Abdi
Publikováno v:
Research and Practice in Thrombosis and Haemostasis
Research and Practice in Thrombosis and Haemostasis, Vol 4, Iss 3, Pp 377-385 (2020)
RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS
Research and Practice in Thrombosis and Haemostasis, 4(3), 377-385. WILEY
Research and Practice in Thrombosis and Haemostasis, Vol 4, Iss 3, Pp 377-385 (2020)
RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS
Research and Practice in Thrombosis and Haemostasis, 4(3), 377-385. WILEY
Hemophilia A and B are inherited X‐linked disorders of hemostasis, associated with an increased bleeding tendency. Patients with severe hemophilia have undetectable clotting factor levels and experience spontaneous bleeds. In patients with nonsever