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There are 3162 results for: content related to: Correlation between endogenous VWF :Ag and PK parameters and bleeding frequency in severe haemophilia A subjects during three-times-weekly prophylaxis with rFVIII- FS

  1. You have free access to this content
    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

  2. 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

  3. 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

  4. 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

  5. Changes in von Willebrand factor level and von Willebrand activity with age in type 1 von Willebrand disease

    Haemophilia

    Volume 21, Issue 5, September 2015, Pages: 636–641, N. Rydz, J. Grabell, D. Lillicrap and P. D. James

    Version of Record online : 10 MAR 2015, DOI: 10.1111/hae.12664

  6. A two-centre comparative evaluation of new automated assays for von Willebrand factor ristocetin cofactor activity and antigen

    Haemophilia

    Volume 20, Issue 1, January 2014, Pages: 147–153, F. Stufano, A. S. Lawrie, S. La Marca, C. Berbenni, L. Baronciani and F. Peyvandi

    Version of Record online : 12 SEP 2013, DOI: 10.1111/hae.12264

  7. Effects of moderate-intensity physical exercise on pharmacokinetics of factor VIII and von Willebrand factor in young adults with severe haemophilia A: a pilot study

    Haemophilia

    Volume 22, Issue 3, May 2016, Pages: e177–e183, N. Zourikian, C. Merlen, A. Bonnefoy, J. St-Louis and G. E. Rivard

    Version of Record online : 14 MAR 2016, DOI: 10.1111/hae.12869

  8. Increased amounts of von Willebrand factor are bound to microparticles after infusion of desmopressin

    Haemophilia

    Volume 19, Issue 2, March 2013, Pages: 236–241, A. Trummer, B. Haarmeijer, S. Werwitzke, C. Wermes, A. Ganser, U. Budde and A. Tiede

    Version of Record online : 11 OCT 2012, DOI: 10.1111/hae.12032

  9. You have full text access to this OnlineOpen article
    A comparative evaluation of a new automated assay for von Willebrand factor activity

    Haemophilia

    Volume 19, Issue 2, March 2013, Pages: 338–342, A. S. Lawrie, F. Stufano, M. T. Canciani, I. J. Mackie, S. J. Machin and F. Peyvandi

    Version of Record online : 4 DEC 2012, DOI: 10.1111/hae.12064

  10. von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients

    Haemophilia

    Volume 22, Issue 6, November 2016, Pages: e502–e511, M. T. Pagliari, L. Baronciani, F. Stufano, I. Garcia-Oya, G. Cozzi, F. Franchi and F. Peyvandi

    Version of Record online : 26 OCT 2016, DOI: 10.1111/hae.13084

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

    Haemophilia

    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

    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

  13. 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

  14. Obesity in haemophilia patients: effect on bleeding frequency, clotting factor concentrate usage, and haemostatic and fibrinolytic parameters

    Haemophilia

    Volume 19, Issue 5, September 2013, Pages: 744–752, A. Tuinenburg, S. Biere-Rafi, M. Peters, P. Verhamme, K. Peerlinck, M. J. H. A. Kruip, B. A. P. Laros-Van Gorkom, M. Roest, J. C. M. Meijers, P. W. Kamphuisen and R. E. G. Schutgens

    Version of Record online : 10 MAY 2013, DOI: 10.1111/hae.12182

  15. Achievements, challenges and unmet needs for haemophilia patients with inhibitors

    Haemophilia

    Volume 22, Issue S1, January 2016, Pages: 1–24, Y. Dargaud, A. Pavlova, S. Lacroix-Desmazes, K. Fischer, M. Soucie, S. Claeyssens, D.w. Scott, R. d'Oiron, G. Lavigne-Lissalde, G. Kenet, C. Escuriola Ettingshausen, A. Borel-Derlon, T. Lambert, G. Pasta and C. Négrier

    Version of Record online : 5 JAN 2016, DOI: 10.1111/hae.12860

  16. Variability in platelet- and collagen-binding defects in type 2M von Willebrand disease

    Haemophilia

    Volume 19, Issue 4, July 2013, Pages: 590–594, D. M. Larsen, S. L. Haberichter, J. C. Gill, A. D. Shapiro and V. H. Flood

    Version of Record online : 18 MAR 2013, DOI: 10.1111/hae.12117

  17. Usefulness of an in vitro cellular expression model for haemophilia A carrier diagnosis: illustration with five novel mutations in the F8 gene in women with isolated factor VIII:C deficiency

    Haemophilia

    Volume 21, Issue 3, May 2015, Pages: e202–e209, O. Roualdes, C. Nougier, M. Fretigny, E. Talagrand, B. Durand, C. Negrier and C. Vinciguerra

    Version of Record online : 24 FEB 2015, DOI: 10.1111/hae.12651

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    Managing Haemophilia for Life: 4th Haemophilia Global Summit

    Haemophilia

    Volume 20, Issue s5, July 2014, Pages: 1–20, J. Astermark, G. Dolan, T. Hilberg, V. Jiménez-Yuste, M. Laffan, R. Lassila, S. Lobet, C. Martinoli and C.-F. Perno

    Version of Record online : 13 JUN 2014, DOI: 10.1111/hae.12468

  19. Quantification of perioperative changes in von Willebrand factor and factor VIII during elective orthopaedic surgery in normal individuals

    Haemophilia

    Volume 19, Issue 5, September 2013, Pages: 758–764, A. Kahlon, J. Grabell, A. Tuttle, D. Engen, W. Hopman, D. Lillicrap and P. James

    Version of Record online : 28 MAY 2013, DOI: 10.1111/hae.12185

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    State of the art: von Willebrand disease

    Haemophilia

    Volume 22, Issue S5, July 2016, Pages: 54–59, A. H. James, J. Eikenboom and A. B. Federici

    Version of Record online : 13 JUL 2016, DOI: 10.1111/hae.12984