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Journal Abstract Search

569 related items for PubMed ID: 15485464

  • 1. Evaluation of primary haemostasis in people with neurofibromatosis type 1.
    Favaloro EJ, Zafer M, Nair SC, Hertzberg M, North K.
    Clin Lab Haematol; 2004 Oct; 26(5):341-5. PubMed ID: 15485464
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  • 2. von Willebrand disease in a pediatric-based population--comparison of type 1 diagnostic criteria and use of the PFA-100 and a von Willebrand factor/collagen-binding assay.
    Dean JA, Blanchette VS, Carcao MD, Stain AM, Sparling CR, Siekmann J, Turecek PL, Lillicrap D, Rand ML.
    Thromb Haemost; 2000 Sep; 84(3):401-9. PubMed ID: 11019962
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  • 3. PFA-100 monitoring of von Willebrand factor (VWF) responses to desmopressin (DDAVP) and factor VIII/VWF concentrate substitution in von Willebrand disease type 1 and 2.
    van Vliet HH, Kappers-Klunne MC, Leebeek FW, Michiels JJ.
    Thromb Haemost; 2008 Sep; 100(3):462-8. PubMed ID: 18766263
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  • 4. Platelet von Willebrand factor determination does not improve the diagnosis of patients with suspected Type 1 von Willebrand disease.
    Shihong I, Morris D, Konkle BA.
    Haemophilia; 2009 Jan; 15(1):131-4. PubMed ID: 18976254
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  • 7. Comparison of the O'Brien filter test and the PFA-100 platelet analyzer in the laboratory diagnosis of von Willebrand's disease.
    Schlammadinger A, Kerenyi A, Muszbek L, Boda Z.
    Thromb Haemost; 2000 Jul; 84(1):88-92. PubMed ID: 10928476
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  • 10. Evaluation of desmopressin effects on haemostasis in children with congenital bleeding disorders.
    Hanebutt FL, Rolf N, Loesel A, Kuhlisch E, Siegert G, Knoefler R.
    Haemophilia; 2008 May; 14(3):524-30. PubMed ID: 18284449
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  • 11. Blood coagulation, fibrinolytic activity and lipid profile in subclinical thyroid disease: subclinical hyperthyroidism increases plasma factor X activity.
    Erem C.
    Clin Endocrinol (Oxf); 2006 Mar; 64(3):323-9. PubMed ID: 16487444
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  • 12. Laboratory monitoring of therapy in von Willebrand disease: efficacy of the PFA-100 and von Willebrand factor:collagen-binding activity as coupled strategies.
    Favaloro EJ.
    Semin Thromb Hemost; 2006 Sep; 32(6):566-76. PubMed ID: 16977567
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  • 13. Characterization of recessive severe type 1 and 3 von Willebrand Disease (VWD), asymptomatic heterozygous carriers versus bloodgroup O-related von Willebrand factor deficiency, and dominant type 1 VWD.
    Michiels JJ, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, van de Velde A, van Vliet H.
    Clin Appl Thromb Hemost; 2006 Jul; 12(3):277-95. PubMed ID: 16959681
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  • 14. Utility of the platelet function analyser (PFA-100/200) for exclusion or detection of von Willebrand disease: A study 22 years in the making.
    Favaloro EJ.
    Thromb Res; 2020 Apr; 188():17-24. PubMed ID: 32036157
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  • 15. von Willebrand disease: a laboratory approach.
    Trasi S, Ghosh K, Shetty S, Mohanty D.
    Natl Med J India; 2005 Apr; 18(2):78-84. PubMed ID: 15981443
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  • 18. Potential laboratory misdiagnosis of hemophilia and von Willebrand disorder owing to cold activation of blood samples for testing.
    Favaloro EJ, Soltani S, McDonald J.
    Am J Clin Pathol; 2004 Nov; 122(5):686-92. PubMed ID: 15491964
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  • 19. Laboratory diagnosis and monitoring of desmopressin treatment of von Willebrand's disease by flow cytometry.
    Giannini S, Mezzasoma AM, Leone M, Gresele P.
    Haematologica; 2007 Dec; 92(12):1647-54. PubMed ID: 18055988
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  • 20. Use of the PFA-100 in the assessment of primary, platelet-related hemostasis in a pediatric setting.
    Rand ML, Carcao MD, Blanchette VS.
    Semin Thromb Hemost; 1998 Dec; 24(6):523-9. PubMed ID: 10066147
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