Zobrazeno 1 - 10
of 10
pro vyhledávání: '"E M, De Wee"'
Autor:
Julianne Cynthia, de Ruiter, Judi Nani Annet, van Diessen, Egbert Frederik, Smit, Vincent, van der Noort, Ronald Alphons Maria, Damhuis, Koen Johan, Hartemink, E M, de Wee
Publikováno v:
ESLUNG group 2022, ' Minimally invasive lobectomy versus stereotactic ablative radiotherapy for stage I non-small cell lung cancer ', European Journal of Cardio-thoracic Surgery, vol. 62, no. 3 . https://doi.org/10.1093/ejcts/ezac118
European Journal of Cardio-Thoracic Surgery, 62(3). OXFORD UNIV PRESS INC
European Journal of Cardio-thoracic Surgery, 62(3). Elsevier
European Journal of Cardio-thoracic Surgery, 62(3):ezac118. Elsevier
European Journal of Cardio-Thoracic Surgery, 62(3). OXFORD UNIV PRESS INC
European Journal of Cardio-thoracic Surgery, 62(3). Elsevier
European Journal of Cardio-thoracic Surgery, 62(3):ezac118. Elsevier
OBJECTIVES A minimally invasive lobectomy (MIL) is the standard treatment for stage I non-small cell lung cancer (NSCLC) in medically operable patients. Stereotactic ablative radiotherapy (SABR) is recommended for inoperable patients and has been pro
Autor:
E M, de Wee, S, van der Sar-van der Brugge, M, Grootenboers, R G, Bentvelsen, K M, Kant, C H, van der Leest
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 164
Covid-19 infection is now a pandemic disease. Most patients have mild symptoms without the need for hospitalization. On average, 5% of the COVID-19-positive patients have severe respiratory symptoms. We present 3 patients aged 45, 67 and 75 years, wh
Autor:
G. Mulders, E. M. De Wee, Frank W.G. Leebeek, E. J. Elfrink, M. C. V. M. Vahedi Nikbakht-Van De Sande, Marieke J. H. A. Kruip
Publikováno v:
Haemophilia. 18:693-698
Summary. Home treatment of haemophilia is currently the standard of care for patients with severe haemophilia. Home treatment increases the responsibility of the patients for their own treatment and care. Therefore, it is of utmost importance to atta
Autor:
Y.V. Sanders, Pieter Willem Kamphuisen, B.A. Laros-Van Gorkum, Karin Fijnvandraat, J. Eikenboom, Marjon H. Cnossen, M. Degenaar-Dujardin, E. P. Mauser Bunschoten, Karina Meijer, E. M. De Wee, J. G. van der Bom
Publikováno v:
Haemophilia. 18:11-51
Background and Aims: Von Willebrand disease (VWD) is caused by reduced levels of or dysfunctional von Willebrand factor (VWF) and is characterized by a bleeding tendency. It is well known that individuals with high VWF levels have a higher risk for a
Autor:
Eveline P. Mauser-Bunschoten, J. G. van der Bom, G. Goverde, B. A. P. Laros-van Gorkom, H. C. J. Eikenboom, Karin Fijnvandraat, Karina Meijer, E. M. De Wee, Dingeman C. Rijken, Frank W.G. Leebeek, P. W. G. Van Der Linden, K. Klaij
Publikováno v:
Haemophilia. 18:444-451
Patients with von Willebrand disease (VWD), the most common inherited bleeding disorder, display large variation in bleeding tendency, which is not completely related to VWF levels. The cause of variability in clinical expression is largely unknown.
Autor:
G, Mulders, E M, de Wee, M C V M, Vahedi Nikbakht-Van de Sande, M J H A, Kruip, E J, Elfrink, F W G, Leebeek
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 18(5)
Home treatment of haemophilia is currently the standard of care for patients with severe haemophilia. Home treatment increases the responsibility of the patients for their own treatment and care. Therefore, it is of utmost importance to attain a high
Autor:
Abbas Dehghan, M. P. M. de Maat, André G. Uitterlinden, Albert Hofman, Jacqueline C. M. Witteman, Marieke J. H. A. Kruip, Frank W.G. Leebeek, E. M. De Wee
Publikováno v:
Journal of Thrombosis and Haemostasis, 9(12), 2509-2511. Wiley-Blackwell Publishing Ltd
Autor:
E M, De Wee, K, Klaij, H C J, Eikenboom, J G, Van Der Bom, K, Fijnvandraat, B A P, Laros-Van Gorkom, E P, Mauser-Bunschoten, K, Meijer, G, Goverde, P W G, Van Der Linden, D C, Rijken, F W G, Leebeek
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 18(3)
Patients with von Willebrand disease (VWD), the most common inherited bleeding disorder, display large variation in bleeding tendency, which is not completely related to VWF levels. The cause of variability in clinical expression is largely unknown.
Autor:
M. Degenaar-Dujardin, F. W. G. Leebeek, H.M. Knol, A. de Goede-Bolder, Sonja Zweegman, Karina Meijer, Jeroen Eikenboom, B. A. P. Laros-van Gorkom, Paula F. Ypma, E. M. De Wee, J. G. van der Bom, Karin Fijnvandraat, Eveline P. Mauser-Bunschoten
Publikováno v:
de Wee, E M, Knol, H M, Mauser-Bunschoten, E P, van der Bom, J G, Eikenboom, J C J, Fijnvandraat, K, de Goede-Bolder, A, Laros-van Gorkom, B, Ypma, P F, Zweegman, S, Meijer, K & Leebeek, F W G 2011, ' Gynaecological and obstetric bleeding in moderate and severe von Willebrand disease ', Thrombosis and Haemostasis, vol. 106, no. 5, pp. 885-892 . https://doi.org/10.1160/TH11-03-0180
Thrombosis and Haemostasis, 106(5), 885-892. Georg Thieme Verlag
Thrombosis and haemostasis, 106(5), 885-892. Schattauer GmbH
Thrombosis and Haemostasis, 106(5), 885-892. Schattauer GmbH
Thrombosis and Haemostasis, 106(5), 885-892
Thrombosis and Haemostasis, 106(5), 885-892. GEORG THIEME VERLAG KG
Thrombosis and Haemostasis, 106, 5, pp. 885-92
Thrombosis and Haemostasis, 106, 885-92
Thrombosis and Haemostasis, 106(5), 885-892. Georg Thieme Verlag
Thrombosis and haemostasis, 106(5), 885-892. Schattauer GmbH
Thrombosis and Haemostasis, 106(5), 885-892. Schattauer GmbH
Thrombosis and Haemostasis, 106(5), 885-892
Thrombosis and Haemostasis, 106(5), 885-892. GEORG THIEME VERLAG KG
Thrombosis and Haemostasis, 106, 5, pp. 885-92
Thrombosis and Haemostasis, 106, 885-92
Contains fulltext : 95943.pdf (Publisher’s version ) (Closed access) A nation-wide cross-sectional study was initiated to assess gynaecological and obstetrical symptoms in an unselected cohort of women with moderate and severe von Willebrand diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c92f1a540a89652e1ce1dd3dc53d3484
https://research.vumc.nl/en/publications/2bd91856-6ad2-4a0b-bb40-c8b4592bff18
https://research.vumc.nl/en/publications/2bd91856-6ad2-4a0b-bb40-c8b4592bff18
Publikováno v:
Haemophilia, 14(5), 1133-1134. Wiley-Blackwell Publishing Ltd