Search Results

There are 41686 results for: content related to: Detection of bleeding disorders in Lebanon: outcomes of a pilot programme

  1. Relative contributions of bleeding scores and iron status on health-related quality of life in von Willebrand disease: a cross-sectional study


    Y. Xu, M. Deforest, J. Grabell, W. Hopman and P. James

    Version of Record online : 9 SEP 2016, DOI: 10.1111/hae.13062

  2. Use of global assays to understand clinical phenotype in congenital factor VII deficiency


    Volume 19, Issue 5, September 2013, Pages: 765–772, L. A. Greene, N. A. Goldenberg, M. L. Simpson, E. Villalobos-Menuey, C. Bombardier, S. S. Acharya, P. J. Santiago-Borrero, A. Cambara and D. M. DiMichele

    Version of Record online : 20 MAY 2013, DOI: 10.1111/hae.12160

  3. Haemophilia A carriers experience reduced health-related quality of life


    Volume 21, Issue 6, November 2015, Pages: 761–765, L. Gilbert, A. Paroskie, D. Gailani, M. R. Debaun and R. F. Sidonio

    Version of Record online : 30 APR 2015, DOI: 10.1111/hae.12690

  4. You have free access to this content
    Third Åland islands conference on von Willebrand disease, 26–28 September 2012: meeting report


    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

  5. Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements


    Volume 20, Issue 4, July 2014, Pages: 550–558, M. Trossaert, A. Lienhart, C. Nougier, M. Fretigny, M. Sigaud, S. Meunier, M. Fouassier, C. Ternisien, C. Negrier and Y. Dargaud

    Version of Record online : 12 FEB 2014, DOI: 10.1111/hae.12381

  6. Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency


    Volume 19, Issue 6, November 2013, Pages: 893–897, M. Borhany, H. Boijout, J.-L. Pellequer, T. Shamsi, G. Moulis, P. Aguilar-Martinez, J.-F. Schved and M. Giansily-Blaizot

    Version of Record online : 4 JUN 2013, DOI: 10.1111/hae.12186

  7. Evaluation of the utility of the ISTH-BAT in haemophilia carriers: a multinational study


    Volume 22, Issue 6, November 2016, Pages: 912–918, P. D. James, J. Mahlangu, C. Bidlingmaier, M. E. Mingot-Castellano, M. Chitlur, P. F. Fogarty, A. Cuker, M. E. Mancuso, P. A. Holme, J. Grabell, N. Satkunam, W. M. Hopman, P. Mathew and on behalf of Global Emerging HEmostasis Experts Panel (GEHEP)

    Version of Record online : 21 NOV 2016, DOI: 10.1111/hae.13089

  8. An approach to outreach patients with von Willebrand disease in Egypt by targeting women with heavy menstrual bleeding and/or bleeding symptoms


    Volume 20, Issue 2, March 2014, Pages: 238–243, N. Sherif, H. Goubran, A. Hassan, T. Burnouf and M. El-Ekiaby

    Version of Record online : 20 NOV 2013, DOI: 10.1111/hae.12335

  9. Association between bleeding tendency and health-related quality of life in carriers of moderate and severe haemophilia


    Volume 21, Issue 6, November 2015, Pages: 742–746, A. Olsson, M. Hellgren, E. Berntorp and F. Baghaei

    Version of Record online : 8 SEP 2015, DOI: 10.1111/hae.12796

  10. The biological efficacy profile of BAX 855, a PEGylated recombinant factor VIII molecule


    Volume 21, Issue 1, January 2015, Pages: 58–63, L. A. Valentino, L. Cong, C. Enockson, X. Song, F. Scheiflinger, E. M. Muchitsch, P. L. Turecek and N. Hakobyan

    Version of Record online : 2 DEC 2014, DOI: 10.1111/hae.12532

  11. Acquired von Willebrand syndrome in patients with overt hypothyroidism: a prospective cohort study


    Volume 20, Issue 3, May 2014, Pages: 326–332, D. J. F. Stuijver, E. Piantanida, B. van Zaane, L. Galli, E. Romualdi, M. L. Tanda, J. C. M. Meijers, H. R. Büller, V. E. A. Gerdes and A. Squizzato

    Version of Record online : 14 OCT 2013, DOI: 10.1111/hae.12275

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


    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

  13. Utility of a Paediatric Bleeding Questionnaire as a screening tool for von Willebrand disease in apparently healthy children


    Volume 21, Issue 6, November 2015, Pages: 806–811, N. Mittal, R. Naridze, P. James, S. Shott and L. A. Valentino

    Version of Record online : 16 MAY 2015, DOI: 10.1111/hae.12689

  14. The accuracy of a patient or parent-administered bleeding assessment tool administered in a paediatric haematology clinic


    Volume 20, Issue 6, November 2014, Pages: 807–813, A. T. Lang, M. S. Sturm, T. Koch, M. Walsh, L. P. Grooms and S. H. O'Brien

    Version of Record online : 9 OCT 2014, DOI: 10.1111/hae.12483

  15. Generation and optimization of the self-administered bleeding assessment tool and its validation as a screening test for von Willebrand disease


    Volume 21, Issue 5, September 2015, Pages: e384–e388, M. Deforest, J. Grabell, S. Albert, J. Young, A. Tuttle, W. M. Hopman and P. D. James

    Version of Record online : 14 JUL 2015, DOI: 10.1111/hae.12747

  16. You have free access to this content
    Rare bleeding disorders – bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency


    Volume 20, Issue s4, May 2014, Pages: 71–75, P. James, O. Salomon, D. Mikovic and F. Peyvandi

    Version of Record online : 25 APR 2014, DOI: 10.1111/hae.12402

  17. Gynaecological and obstetrical bleeding in women with factor XI deficiency – a systematic review


    Volume 22, Issue 2, March 2016, Pages: 188–195, S. Wiewel-Verschueren, I. J. Arendz, H. M. Knol and K. Meijer

    Version of Record online : 3 DEC 2015, DOI: 10.1111/hae.12856

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


    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

  19. A single-centre study of haemostatic outcomes of joint replacement in von Willebrand disease and control patients and an analysis of the literature


    Volume 22, Issue 6, November 2016, Pages: 934–942, L. Rugeri, A. A. Ashrani, W. L. Nichols, R. T. Trousdale and R. K. Pruthi

    Version of Record online : 6 JUL 2016, DOI: 10.1111/hae.13027

  20. Oral surgery-associated postoperative bleeding in haemophilia patients – a tertiary centre's two decade experience


    Volume 21, Issue 2, March 2015, Pages: 234–240, N. Givol, A. Hirschhorn, A. Lubetsky, D. Bashari and G. Kenet

    Version of Record online : 4 DEC 2014, DOI: 10.1111/hae.12573