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There are 3131 results for: content related to: An approach to outreach patients with von Willebrand disease in Egypt by targeting women with heavy menstrual bleeding and/or bleeding symptoms

  1. Type 2M von Willebrand disease – more often misidentified than correctly identified

    Haemophilia

    Volume 22, Issue 3, May 2016, Pages: e145–e155, E. J. Favaloro, R. A. Bonar, S. Mohammed, A. Arbelaez, J. Niemann, R. Freney, M. Meiring, J. Sioufi and K. Marsden

    Version of Record online : 31 MAR 2016, DOI: 10.1111/hae.12903

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    Third Åland islands conference on von Willebrand disease, 26–28 September 2012: meeting report

    Haemophilia

    Volume 19, Issue s3, March 2013, Pages: 1–18, E. Berntorp, B. Fuchs, M. Makris, R. Montgomery, V. Flood, J. S. O'Donnell, A. B. Federici, D. Lillicrap, P. James, U. Budde, M. Morfini, P. Petrini, S. Austin, C. Kannicht, V. Jiménez-Yuste and C. Lee

    Version of Record online : 6 FEB 2013, DOI: 10.1111/hae.12078

  3. Diagnosis of inherited von Willebrand disease: comparison of two methodologies and analysis of the discrepancies

    Haemophilia

    Volume 20, Issue 4, July 2014, Pages: 559–567, J. Costa-Pinto, A. Pérez-Rodríguez, M. del C. Goméz-del-Castillo, E. Lourés, Á. Rodríguez-Trillo, J. Batlle and M. F. López-Fernández

    Version of Record online : 21 FEB 2014, DOI: 10.1111/hae.12380

  4. von Willebrand's disease: a report from a meeting in the Åland islands

    Haemophilia

    Volume 18, Issue s6, September 2012, Pages: 1–13, E. Berntorp, I. Peake, U. Budde, M. Laffan, R. Montgomery, J. Windyga, A. Goodeve, P. Petrini, M. von Depka, W. Miesbach, D. Lillicrap, A. B. Federici, R. Lassila and G. White

    Version of Record online : 21 AUG 2012, DOI: 10.1111/j.1365-2516.2012.02925.x

  5. Practical aspects of DDAVP use in patients with von Willebrand Disease undergoing invasive procedures: a European survey

    Haemophilia

    Volume 22, Issue 1, January 2016, Pages: 110–120, J. Windyga, G. Dolan, C. Altisent, O. Katsarou, M.-F. López Fernández, B. Zülfikar and on behalf of the EHTSB

    Version of Record online : 24 JUL 2015, DOI: 10.1111/hae.12763

  6. Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional study

    Haemophilia

    Volume 21, Issue 3, May 2015, Pages: e185–e192, K. P. M. van Galen, Y. V. Sanders, U. Vojinovic, J. Eikenboom, M. H. Cnossen, R. E. G. Schutgens, J. G. van der Bom, K. Fijnvandraat, B. A. P. Laros-Van Gorkom, K. Meijer, F. W. G. Leebeek, E. P. Mauser-Bunschoten and for the WiN Study Group

    Version of Record online : 9 APR 2015, DOI: 10.1111/hae.12670

  7. Bleeding disorders, menorrhagia and iron deficiency: impacts on health-related quality of life

    Haemophilia

    Volume 19, Issue 3, May 2013, Pages: 385–391, C. Rae, W. Furlong, J. Horsman, E. Pullenayegum, C. Demers, J. St-Louis, D. Lillicrap and R. Barr

    Version of Record online : 21 SEP 2012, DOI: 10.1111/hae.12014

  8. Baseline factor VIII plasma levels and age at first bleeding in patients with severe forms of von Willebrand disease

    Haemophilia

    S. M. Siboni, E. Biguzzi, V. Caiani, C. Mistretta, P. Bucciarelli and F. Peyvandi

    Version of Record online : 4 FEB 2016, DOI: 10.1111/hae.12900

  9. Practical aspects of factor concentrate use in patients with von Willebrand disease undergoing invasive procedures: a European survey

    Haemophilia

    J. Windyga, G. Dolan, C. Altisent, O. Katsarou, M.-F. López Fernández, B. Zülfikar and on behalf of the EHTSB

    Version of Record online : 13 JUN 2016, DOI: 10.1111/hae.12955

  10. Comparison of von Willebrand factor (VWF) activity levels determined by HemosIL AcuStar assay and HemosIL LIA assay with ristocetin cofactor assay by aggregometry

    Haemophilia

    Volume 22, Issue 3, May 2016, Pages: e200–e207, S. Sagheer, S. Rodgers, O. Yacoub, R. Dauer, S. Mcrae and E. Duncan

    Version of Record online : 14 APR 2016, DOI: 10.1111/hae.12937

  11. Joint surgery in von Willebrand disease: a multicentre cross-sectional study

    Haemophilia

    Volume 22, Issue 2, March 2016, Pages: 256–262, K. P. M. van Galen, K. Meijer, H. C. Vogely, J. Eikenboom, R. E. G. Schutgens, M. H. Cnossen, K. Fijnvandraat, J. G. van der Bom, B. A. P. Laros-van Gorkom, F. W. G. Leebeek, E. P. Mauser-Bunschoten and for the WiN study group

    Version of Record online : 9 NOV 2015, DOI: 10.1111/hae.12834

  12. Comprehensive evaluation of haemostatic function in von Willebrand disease patients using a microchip-based flow chamber system

    Haemophilia

    Volume 21, Issue 1, January 2015, Pages: 71–80, K. Ogiwara, K. Nogami, K. Hosokawa, T. Ohnishi, T. Matsumoto and M. Shima

    Version of Record online : 29 DEC 2014, DOI: 10.1111/hae.12610

  13. Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in von Willebrand disease

    Haemophilia

    Volume 20, Issue 4, July 2014, Pages: e311–e317, F. Ahmad, F. Oyen, R. Jan, U. Budde, R. Schneppenheim and R. Saxena

    Version of Record online : 8 APR 2014, DOI: 10.1111/hae.12441

  14. Desmopressin (DDAVP) in the management of patients with congenital bleeding disorders

    Haemophilia

    Volume 20, Issue 2, March 2014, Pages: 158–167, C. Leissinger, M. Carcao, J. C. Gill, J. Journeycake, T. Singleton and L. Valentino

    Version of Record online : 12 AUG 2013, DOI: 10.1111/hae.12254

  15. Similarity in joint function limitation in Type 3 von Willebrand's disease and moderate haemophilia A

    Haemophilia

    Volume 19, Issue 4, July 2013, Pages: 595–601, S. L. Sood, A. Cuker, C. Wang, A. D. Metjian, E. Y. Chiang, J. M. Soucie, B. A. Konkle and HTCN Study Investigators

    Version of Record online : 28 MAR 2013, DOI: 10.1111/hae.12119

  16. Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease

    Haemophilia

    V. Daidone, G. Barbon, M. G. Cattini, E. Pontara, C. Romualdi, I. Di Pasquale, K. Hosokawa and A. Casonato

    Version of Record online : 13 JUN 2016, DOI: 10.1111/hae.12971

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    von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)

    Haemophilia

    Volume 14, Issue 2, March 2008, Pages: 171–232, W. L. NICHOLS, M. B. HULTIN, A. H. JAMES, M. J. MANCO-JOHNSON, R. R. MONTGOMERY, T. L. ORTEL, M. E. RICK, J. E. SADLER, M. WEINSTEIN and B. P. YAWN

    Version of Record online : 28 FEB 2008, DOI: 10.1111/j.1365-2516.2007.01643.x

  18. Clinical phenotype in genetically confirmed von Willebrand disease type 2N patients reflects a haemophilia A phenotype

    Haemophilia

    Volume 21, Issue 5, September 2015, Pages: e375–e383, M. E. R. van Meegeren, T. L. Mancini, S. C. M. Schoormans, B. J. T. van Haren, C. van Duren, A. Diekstra, B. A. P. Laros-van Gorkom, P. P. T. Brons, A. Simons, L. Hoefsloot and W. L. van Heerde

    Version of Record online : 24 JUL 2015, DOI: 10.1111/hae.12733

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    Laboratory aspects of von Willebrand disease: test repertoire and options for activity assays and genetic analysis

    Haemophilia

    Volume 20, Issue s4, May 2014, Pages: 65–70, G. Castaman, A. Hillarp and A. Goodeve

    Version of Record online : 25 APR 2014, DOI: 10.1111/hae.12410

  20. You have free access to this content
    von Willebrand disease and platelet disorders

    Haemophilia

    Volume 20, Issue s4, May 2014, Pages: 59–64, E. J. Favaloro, I. Bodó, S. J. Israels and S. A. Brown

    Version of Record online : 25 APR 2014, DOI: 10.1111/hae.12414