Haemophilia

Cover image for Vol. 18 Issue 3

May 2012

Volume 18, Issue 3

Pages 305–481, e60–e346

  1. Commemorative Article

    1. Top of page
    2. Commemorative Article
    3. Review Articles
    4. Original Articles
    5. Meeting Report
    6. Abstracts
    7. Online Letters
    8. How We Treat
    9. May 2012 Online Supplement
    1. You have free access to this content
      Porcine factor VIII (pages 305–309)

      P. L. F. GIANGRANDE

      Version of Record online: 25 APR 2012 | DOI: 10.1111/j.1365-2516.2012.02803.x

  2. Review Articles

    1. Top of page
    2. Commemorative Article
    3. Review Articles
    4. Original Articles
    5. Meeting Report
    6. Abstracts
    7. Online Letters
    8. How We Treat
    9. May 2012 Online Supplement
    1. Exploring the biological basis of haemophilic joint disease: experimental studies (pages 310–318)

      L. A. VALENTINO, N. HAKOBYAN, C. ENOCKSON, M. L. SIMPSON, N. C. KAKODKAR, L. CONG and X. SONG

      Version of Record online: 2 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02669.x

    2. Recommendations for assessment, monitoring and follow-up of patients with haemophilia (pages 319–325)

      P. DE MOERLOOSE, K. FISCHER, T. LAMBERT, J. WINDYGA, A. BATOROVA, G. LAVIGNE-LISSALDE, A. ROCINO, J. ASTERMARK and C. HERMANS

      Version of Record online: 13 OCT 2011 | DOI: 10.1111/j.1365-2516.2011.02671.x

  3. Original Articles

    1. Top of page
    2. Commemorative Article
    3. Review Articles
    4. Original Articles
    5. Meeting Report
    6. Abstracts
    7. Online Letters
    8. How We Treat
    9. May 2012 Online Supplement
    1. Clinical haemophilia

      Outcomes of mentored, grant-funded fellowship training in haemostasis /thrombosis: findings from a nested case–control survey study (pages 326–331)

      N. A. GOLDENBERG, R. KRUSE-JARRES, N. FRICK, S. W. PIPE, C. A. LEISSINGER and C. M. KESSLER

      Version of Record online: 7 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02626.x

    2. Healthcare resource utilization among haemophilia A patients in the United States (pages 332–338)

      L. A. VALENTINO, S. W. PIPE, M. D. TARANTINO, X. YE, Y. XIONG and M. P. LUO

      Version of Record online: 2 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02677.x

    3. Deaths associated with acquired haemophilia in France from 2000 to 2009: multiple cause analysis for best care strategies (pages 339–344)

      A. AOUBA, G. REY, G. PAVILLON, E. JOUGLA, C. ROTHSCHILD, M-F. TORCHET, L. GUILLEVIN, O. HERMINE and A. AOUBA

      Version of Record online: 12 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02647.x

    4. Quality of life

      Health-related quality of life and psychological well-being in elderly patients with haemophilia (pages 345–352)

      S. VON MACKENSEN, A. GRINGERI, S. M. SIBONI, P. M. MANNUCCI and FOR THE ITALIAN ASSOCIATION OF HAEMOPHILIA CENTRES (AICE)

      Version of Record online: 12 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02643.x

    5. Cross-cultural validation of the CHO-KLAT and HAEMO-QoL-A in Canadian French (pages 353–357)

      N. L. YOUNG, J. ST-LOUIS, T. BURKE, L. HERSHON and V. BLANCHETTE

      Version of Record online: 21 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02703.x

    6. Musculoskeletal

    7. Ultrasonography of haemophilic arthropathy (pages 364–368)

      M. MUÇA-PERJA, S. RIVA, B. GROCHOWSKA, L. MANGIAFICO, D. MAGO and A. GRINGERI

      Version of Record online: 17 OCT 2011 | DOI: 10.1111/j.1365-2516.2011.02672.x

    8. Inhibitors

      F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity (pages 375–382)

      C. H. MILLER, J. BENSON, D. ELLINGSEN, J. DRIGGERS, A. PAYNE, F. M. KELLY, J. M. SOUCIE, W. CRAIG HOOPER and THE HEMOPHILIA INHIBITOR RESEARCH STUDY INVESTIGATORS

      Version of Record online: 21 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02700.x

    9. Efficacy of FEIBA for acute bleeding and surgical haemostasis in haemophilia A patients with inhibitors: a multicentre registry in Turkey (pages 383–391)

      B. ZÜLFIKAR, G. AYDOGAN, Z. SALCIOGLU, A. F. ONER, K. KAVAKLI, T. GURSEL, H. ZÜLFIKAR and For the FEIBA INVESTIGATORS TEAM

      Version of Record online: 22 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02693.x

    10. Women with inherited bleeding disorders

      Pregnancy in type 2B VWD: a case series (pages 406–412)

      A. RANGER, R. A. MANNING, H. LYALL, M. A. LAFFAN and C. M. MILLAR

      Version of Record online: 14 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02691.x

    11. Paediatrics

    12. Circumcision and complications in patients with haemophilia in southern part of Turkey: Çukurova experience (pages 426–430)

      I. SASMAZ, B. ANTMEN, G. LEBLEBISATAN, B. ŞAHIN KARAGÜN, Y. KILINÇ and R. TUNCER

      Version of Record online: 19 DEC 2011 | DOI: 10.1111/j.1365-2516.2011.02706.x

    13. Rare bleeding disorders

      Pharmacokinetic properties of two different recombinant activated factor VII formulations (pages 431–436)

      M. MORFINI, V. JIMÉNEZ-YUSTE, H. EICHLER, R. FISCHER, C. M. KIRCHMAIER, B. SCHARLING and J. BJERRE

      Version of Record online: 17 OCT 2011 | DOI: 10.1111/j.1365-2516.2011.02674.x

    14. Laboratory science

      Severe haemophilia A patients have reduced numbers of peripheral memory B cells (pages 437–443)

      M. B. IRIGOYEN, M. E. FELIPPO, L. PRIMIANI, M. CANDELA, R. P. BIANCO, M. M. DE BRACCO and N. GALASSI

      Version of Record online: 12 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02642.x

    15. Effect of fibrinolysis on bleeding phenotype in moderate and severe von Willebrand disease (pages 444–451)

      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 and FOR THE WIN STUDY GROUP

      Version of Record online: 12 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02645.x

    16. Protein C, protein S and von Willebrand factor levels correlate with bleeding symptoms: a population-based study (pages 457–462)

      P. ROJNUCKARIN, N. UAPRASERT, B. AKKAWAT, R. SETTAPIBOON, T. NANAKORN and T. INTRAGUMTORNCHAI

      Version of Record online: 7 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02678.x

    17. Whole blood rotation thromboelastometry (ROTEM®) in nine severe factor V deficient patients and evaluation of the role of intraplatelets factor V (pages 463–468)

      L. SPIEZIA, C. RADU, E. CAMPELLO, C. BULATO, D. BERTINI, G. BARILLARI, V. DE ANGELIS, P. PRADELLA, E. ZANON and P. SIMIONI

      Version of Record online: 19 DEC 2011 | DOI: 10.1111/j.1365-2516.2011.02710.x

  4. Meeting Report

    1. Top of page
    2. Commemorative Article
    3. Review Articles
    4. Original Articles
    5. Meeting Report
    6. Abstracts
    7. Online Letters
    8. How We Treat
    9. May 2012 Online Supplement
    1. Understanding FVIII/VWF complex – report from a symposium of XXIX WFH meeting 2010 (pages 469–475)

      A. GRINGERI, F. A. OFOSU, S. GRANCHA, J. OLDENBURG, N. P. EWING and A. B. FEDERICI

      Version of Record online: 22 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02655.x

  5. Abstracts

    1. Top of page
    2. Commemorative Article
    3. Review Articles
    4. Original Articles
    5. Meeting Report
    6. Abstracts
    7. Online Letters
    8. How We Treat
    9. May 2012 Online Supplement
  6. Online Letters

    1. Top of page
    2. Commemorative Article
    3. Review Articles
    4. Original Articles
    5. Meeting Report
    6. Abstracts
    7. Online Letters
    8. How We Treat
    9. May 2012 Online Supplement
    1. The international factor IX treatment network survey (pages e60–e62)

      E. BERNTORP, A. D. SHAPIRO, J. WATERS, J. ASTERMARK and THE INTERNATIONAL FACTOR IX TREATMENT NETWORK

      Version of Record online: 8 MAR 2012 | DOI: 10.1111/j.1365-2516.2012.02767.x

    2. Invasive procedures and minor surgery in factor VII deficiency (pages e63–e65)

      G. MARIANI, A. DOLCE, M. NAPOLITANO, J. INGERSLEV, M. GIANSILY-BLAIZOT, M. D. DI MINNO, G. AUERSWALD, A. R. DE SAEZ, A. TAGLIAFERRI, A. BATOROVA and ON BEHALF OF THE STER (SEVEN TREATMENT EVALUATION REGISTRY); OTHER AUTHORS ARE LISTED AT THE END OF THE MANUSCRIPT

      Version of Record online: 22 FEB 2012 | DOI: 10.1111/j.1365-2516.2012.02751.x

    3. The challenging management of a child with type 3 von Willebrand disease and antibodies to von Willebrand factor (pages e66–e67)

      H. PERGANTOU, P. XAFAKI, E. ADAMTZIKI, P. KOLETSI, A. KOMITOPOULOU and H. PLATOKOUKI

      Version of Record online: 25 APR 2012 | DOI: 10.1111/j.1365-2516.2012.02799.x

    4. Successful immune tolerance induction in two boys with haemophilia B and inhibitory antibodies (pages e67–e69)

      A. KLUKOWSKA, P. LAGUNA, B. WALESZKIEWICZ-MAJEWSKA, J. PEREGUD-POGORZELSKI, E. KAMIENSKA, P. BIGNELL and P. GIANGRANDE

      Version of Record online: 25 APR 2012 | DOI: 10.1111/j.1365-2516.2012.02784.x

    5. Re-emergence of a low-titre factor VIII inhibitor after liver transplant (pages e69–e71)

      S. HORTON, V. MARTLEW, J. WILDE and J. THACHIL

      Version of Record online: 25 APR 2012 | DOI: 10.1111/j.1365-2516.2012.02811.x

    6. Complete immunotolerance induction after FEIBA prophylaxis in a haemophilia A patient with high-titre inhibitor (pages e75–e77)

      E. NANISHI, S. OHGA, T. DOI, M. ISHIMURA, K. IHARA, H. TAKADA, M. SHIMA and T. HARA

      Version of Record online: 8 MAR 2012 | DOI: 10.1111/j.1365-2516.2012.02776.x

    7. Aphthous oral ulceration and its successful management by Lactobacillus brevis CD2 extract in an adult haemophilic patient (pages e78–e79)

      P. NISCOLA, A. TENDAS, L. SCARAMUCCI, M. GIOVANNINI, V. TRINCHIERI and P. DE FABRITIIS

      Version of Record online: 15 FEB 2012 | DOI: 10.1111/j.1365-2516.2012.02757.x

    8. Pain management issues in haemophilia (pages e81–e82)

      M. D. GOODYEAR and M.-C. POON

      Version of Record online: 20 FEB 2012 | DOI: 10.1111/j.1365-2516.2012.02764.x

    9. Does weight reduction in haemophilia lead to a decrease in joint bleeds? (pages e82–e84)

      S. MAJUMDAR, N. AHMAD, C. KARLSON, A. MORRIS and R. IYER

      Version of Record online: 4 APR 2011 | DOI: 10.1111/j.1365-2516.2011.02521.x

    10. Non-operative management of blunt major hepatic injury in a young adult with severe haemophilia A (pages e84–e86)

      B. M. T. PEREIRA, G. P. FRAGA, E. S. HIRANO, C. V. CARMONA and M. C. OZELO

      Version of Record online: 22 FEB 2012 | DOI: 10.1111/j.1365-2516.2012.02761.x

    11. Acquired factor V deficiency and mini literature review (pages e86–e87)

      H. KUNIMOTO, Y. MIYAKAWA and S. OKAMOTO

      Version of Record online: 12 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02650.x

  7. How We Treat

    1. Top of page
    2. Commemorative Article
    3. Review Articles
    4. Original Articles
    5. Meeting Report
    6. Abstracts
    7. Online Letters
    8. How We Treat
    9. May 2012 Online Supplement
  8. May 2012 Online Supplement

    1. Top of page
    2. Commemorative Article
    3. Review Articles
    4. Original Articles
    5. Meeting Report
    6. Abstracts
    7. Online Letters
    8. How We Treat
    9. May 2012 Online Supplement
    1. Original Articles

      Clinical haemophilia
      A study of variations in the reported haemophilia B prevalence around the world (pages e91–e94)

      J. S. STONEBRAKER, P. H. B. BOLTON-MAGGS, J. MICHAEL SOUCIE, I. WALKER and M. BROOKER

      Version of Record online: 7 JUN 2011 | DOI: 10.1111/j.1365-2516.2011.02588.x

    2. Review Article

      Clinical haemophilia
      Psychosocial aspects of haemophilia: a systematic review of methodologies and findings (pages e101–e114)

      F. R. M. Y CASSIS, F. QUEROL, A. FORSYTH, A. IORIO and ON BEHALF OF THE HERO INTERNATIONAL ADVISORY BOARD

      Version of Record online: 8 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02683.x

    3. Original Articles

      Clinical haemophilia
      A national study of pain in the bleeding disorders community: a description of haemophilia pain (pages e115–e119)

      M. WITKOP, A. LAMBING, G. DIVINE, E. KACHALSKY, D. RUSHLOW and J. DINNEN

      Version of Record online: 16 DEC 2011 | DOI: 10.1111/j.1365-2516.2011.02709.x

    4. A qualitative study identifying the knowledge, attitudes and behaviours of young men with mild haemophilia (pages e120–e125)

      J. NILSON, C. SCHACHTER, K. MULDER, M. HAHN, M. STEELE, P. HILLIARD and C. JAROCK

      Version of Record online: 16 DEC 2011 | DOI: 10.1111/j.1365-2516.2011.02714.x

    5. Emergency and out of hours care of patients with inherited bleeding disorders (pages e126–e131)

      H. FOWLER, R. LACEY, J. KEANEY, C. KAY-JONES, V. MARTLEW and J. THACHIL

      Version of Record online: 19 DEC 2011 | DOI: 10.1111/j.1365-2516.2011.02721.x

    6. Commentary

      Clinical haemophilia
    7. Original Articles

      Clinical haemophilia
    8. Quality of life
      Why should we care about quality of life in persons with haemophilia? (pages e154–e157)

      L. ALEDORT, M. BULLINGER, S. VON MACKENSEN, J. WASSERMAN, N. L. YOUNG, D. GLOBE and ON BEHALF OF THE HEALTH RELATED QUALITY OF LIFE EXPERT WORKING GROUP OF THE INTERNATIONAL PROPHYLAXIS STUDY GROUP

      Version of Record online: 22 FEB 2012 | DOI: 10.1111/j.1365-2516.2012.02771.x

    9. von Willebrand disease (VWD)
      Screening for von Willebrand disease: contribution of an automated assay for von Willebrand factor activity (pages e158–e163)

      D. LASNE, C. DEY, M.-D. DAUTZENBERG, Z. CHERQAOUI, F. MONGE, A. AOUBA, M.-F. TORCHET, D. GELOEN, P. LANDAIS and C. ROTHSCHILD

      Version of Record online: 28 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02662.x

    10. Review Articles

      von Willebrand disease (VWD)
    11. Original Articles

      von Willebrand disease (VWD)
      Haemostatic management of extreme challenges to haemostasis in acquired von Willebrand syndrome (pages e188–e191)

      M. P. COLELLA, G. C. DUARTE, J. F. C. MARQUES JR and E. V. DE PAULA

      Version of Record online: 22 FEB 2012 | DOI: 10.1111/j.1365-2516.2012.02769.x

    12. Commentary

      Rare bleeding disorders
      Challenges of rare disease research: limited patients and competing priorities (pages e192–e194)

      M. V. RAGNI, C. G. MOORE, V. BIAS, N. S. KEY, P. A. KOUIDES, C. W. FRANCIS and for the Hemostasis Thrombosis Research Society (HTRS)

      Version of Record online: 12 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02646.x

    13. Original Articles

      Rare bleeding disorders
      Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India (pages e195–e200)

      A. VISWABANDYA, S. BAIDYA, S. C. NAIR, A. ABRAHAM, B. GEORGE, V. MATHEWS, M. CHANDY and A. SRIVASTAVA

      Version of Record online: 4 JAN 2012 | DOI: 10.1111/j.1365-2516.2011.02730.x

    14. Musculoskeletal
      Viscosupplementation in haemophilic arthropathy: a long-term follow-up study (pages e210–e214)

      C. CARULLI, R. CIVININI, C. MARTINI, S. LINARI, M. MORFINI, M. TANI and M. INNOCENTI

      Version of Record online: 22 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02654.x

    15. Review Article

      Musculoskeletal
    16. Original Articles

      Musculoskeletal
      Functional impact of custom-made foot orthoses in patients with haemophilic ankle arthropathy (pages e227–e235)

      S. LOBET, C. DETREMBLEUR, A.-C. LANTIN, L. HAENECOUR and C. HERMANS

      Version of Record online: 19 DEC 2011 | DOI: 10.1111/j.1365-2516.2011.02711.x

    17. Inhibitors
      Influence of class I and II HLA alleles on inhibitor development in severe haemophilia A patients from the South of Brazil (pages e236–e240)

      M. F. DE BARROS, J. C. M. HERRERO, A. M. SELL, F. C. De MELO, M. A. BRAGA, C. B. PELISSARI, J. MACHADO, S. De SOUZA SCHILLER, L. De SOUZA HIRLE and J. E. L. VISENTAINER

      Version of Record online: 4 JUL 2011 | DOI: 10.1111/j.1365-2516.2011.02604.x

    18. Profiling of differentially expressed genes in haemophilia A with inhibitor (pages e247–e253)

      S. H. HWANG, J. A. LIM, M. J. KIM, H. C. KIM, H. W. LEE, K. Y. YOO, C. W. YOU, K. S. LEE and H. S. KIM

      Version of Record online: 19 DEC 2011 | DOI: 10.1111/j.1365-2516.2011.02702.x

    19. Low prevalence of inhibitor antibodies in the Canadian haemophilia population (pages e254–e259)

      K. E. WEBERT, G. E. RIVARD, J. TEITEL, M. CARCAO, D. LILLICRAP, J. ST-LOUIS and I. R. WALKER

      Version of Record online: 14 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02694.x

    20. Increased prevalence of inhibitors in Hispanic patients with severe haemophilia A enrolled in the Universal Data Collection database (pages e260–e265)

      S. L. CARPENTER, J. MICHAEL SOUCIE, S. STERNER, R. PRESLEY and Hemophilia Treatment Center Network (HTCN) Investigators

      Version of Record online: 18 JAN 2012 | DOI: 10.1111/j.1365-2516.2011.02739.x

    21. Transfusion transmitted infection
      Beneficial effect of successful HCV treatment in patients with inherited bleeding disorders, assessed by liver stiffness measurements (pages e266–e272)

      D. E. FRANSEN van de PUTTE, K. FISCHER, R. J. De KNEGT, D. POSTHOUWER, K. J. Van ERPECUM, D. H. BIESMA and E. P. MAUSER-BUNSCHOTEN

      Version of Record online: 21 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02697.x

    22. Women with inherited bleeding disorders
    23. Factor X deficiency and pregnancy: preconception counselling and therapeutic options (pages e277–e285)

      D. NANCE, N. C. JOSEPHSON, K. PAULYSON-NUNEZ and A. H. JAMES

      Version of Record online: 12 DEC 2011 | DOI: 10.1111/j.1365-2516.2011.02724.x

    24. Adolescence
    25. Paediatrics
      Significance and causes of abnormal preoperative coagulation test results in children (pages e297–e301)

      A. SAMKOVÁ, J. BLATNÝ, V. FIAMOLI, P. DULÍČEK and E. PAŘÍZKOVÁ

      Version of Record online: 4 OCT 2011 | DOI: 10.1111/j.1365-2516.2011.02665.x

    26. Postural adjustment after an unexpected perturbation in children with haemophilia (pages e311–e315)

      F. M. B. De SOUZA, R. P. PEREIRA, N. P. MINUQUE, C. M. Do CARMO, M. H. M. De MELLO, P. VILLAÇA and C. TANAKA

      Version of Record online: 8 MAR 2012 | DOI: 10.1111/j.1365-2516.2012.02768.x

    27. Laboratory science
      Thrombin activatable fibrinolysis inhibitor activation and bleeding in haemophilia A (pages e316–e322)

      J. H. FOLEY, M. E. NESHEIM, G. E. RIVARD and K. E. BRUMMEL-ZIEDINS

      Version of Record online: 20 SEP 2011 | DOI: 10.1111/j.1365-2516.2011.02648.x

    28. Immune response against serial infusion of factor VIII antigen through an implantable venous-access device system in haemophilia A mice (pages e323–e330)

      S. MADOIWA, E. KOBAYASHI, Y. KASHIWAKURA, A. SAKATA, A. YASUMOTO, T. OHMORI, J. MIMURO and Y. SAKATA

      Version of Record online: 2 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02686.x

    29. Genetics
    30. Identification of 123 previously unreported mutations in the F8 gene of Iranian patients with Haemophilia A (pages e340–e346)

      S. RAVANBOD, M. RASSOULZADEGAN, G. RASTEGAR-LARI, M. JAZEBI, S. ENAYAT and F. ALA

      Version of Record online: 28 NOV 2011 | DOI: 10.1111/j.1365-2516.2011.02708.x

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