These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 16430455)

  • 1. The value of genetic testing for type 2B Von Willebrand disease.
    Roland K; Rapson D; Lillicrap D; James P
    Clin Lab Haematol; 2006 Feb; 28(1):17-21. PubMed ID: 16430455
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The role of molecular genetics in diagnosing von Willebrand disease.
    James P; Lillicrap D
    Semin Thromb Hemost; 2008 Sep; 34(6):502-8. PubMed ID: 19085649
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organisation Haemophilia Genetics Laboratory Network.
    Keeney S; Bowen D; Cumming A; Enayat S; Goodeve A; Hill M;
    Haemophilia; 2008 Sep; 14(5):1099-111. PubMed ID: 18637846
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic testing for von Willebrand disease: the Canadian experience.
    James P; Lillicrap D
    Semin Thromb Hemost; 2006 Jul; 32(5):546-52. PubMed ID: 16862529
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diagnosis of inherited von Willebrand disease: a clinical perspective.
    Federici AB
    Semin Thromb Hemost; 2006 Sep; 32(6):555-65. PubMed ID: 16977566
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotypic identification of platelet-type von Willebrand disease and its discrimination from type 2B von Willebrand disease: a question of 2B or not 2B? A story of nonidentical twins? Or two sides of a multidenominational or multifaceted primary-hemostasis coin?
    Favaloro EJ
    Semin Thromb Hemost; 2008 Feb; 34(1):113-27. PubMed ID: 18393148
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Platelet-type von Willebrand disease and type 2B von Willebrand disease: a story of nonidentical twins when two different genetic abnormalities evolve into similar phenotypes.
    Othman M
    Semin Thromb Hemost; 2007 Nov; 33(8):780-6. PubMed ID: 18175283
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inherited and de novo von Willebrand disease 'Vicenza' in UK families with the R1205H mutation: diagnostic pitfalls and new insights.
    Lester WA; Guilliatt AM; Surdhar GK; Enayat SM; Wilde JT; Willoughby S; Grundy P; Cumming AM; Collins PW; Hill FG
    Br J Haematol; 2006 Oct; 135(1):91-6. PubMed ID: 16925796
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance.
    Enayat MS; Guilliatt AM; Lester W; Wilde JT; Williams MD; Hill FG
    Br J Haematol; 2006 Jun; 133(6):664-6. PubMed ID: 16704444
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Laboratory tests for precise classification and genetic analysis of von Willebrand disease.
    Habart D; Vorlová Z
    Sb Lek; 2003; 104(2):237-45. PubMed ID: 14577134
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Laboratory diagnosis of von Willebrand disease type 1/2E (2A subtype IIE), type 1 Vicenza and mild type 1 caused by mutations in the D3, D4, B1-B3 and C1-C2 domains of the von Willebrand factor gene. Role of von Willebrand factor multimers and the von Willebrand factor propeptide/antigen ratio.
    Gadisseur A; Berneman Z; Schroyens W; Michiels JJ
    Acta Haematol; 2009; 121(2-3):128-38. PubMed ID: 19506359
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical, laboratory and therapeutic aspects of platelet-type von Willebrand disease.
    Franchini M; Montagnana M; Lippi G
    Int J Lab Hematol; 2008 Apr; 30(2):91-4. PubMed ID: 18333841
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
    Gupta PK; Saxena R; Adamtziki E; Budde U; Oyen F; Obser T; Schneppenheim R
    Blood Cells Mol Dis; 2008; 41(2):219-22. PubMed ID: 18485763
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Laboratory diagnosis and molecular classification of von Willebrand disease.
    Gadisseur A; Hermans C; Berneman Z; Schroyens W; Deckmyn H; Michiels JJ
    Acta Haematol; 2009; 121(2-3):71-84. PubMed ID: 19506352
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis of von Willebrand disease subtypes: implications for treatment.
    Budde U
    Haemophilia; 2008 Nov; 14 Suppl 5():27-38. PubMed ID: 18786008
    [TBL] [Abstract][Full Text] [Related]  

  • 16. von Willebrand disease: laboratory aspects of diagnosis and treatment.
    Favaloro EJ; Lillicrap D; Lazzari MA; Cattaneo M; Mazurier C; Woods A; Meschengieser S; Blanco A; Kempfer AC; Hubbard A; Chang A
    Haemophilia; 2004 Oct; 10 Suppl 4():164-8. PubMed ID: 15479392
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A practical approach to genetic testing for von Willebrand disease.
    Pruthi RK
    Mayo Clin Proc; 2006 May; 81(5):679-91. PubMed ID: 16706266
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Biology of inherited coagulopathies: von Willebrand factor.
    Ginsburg D
    Hematol Oncol Clin North Am; 1992 Oct; 6(5):1011-20. PubMed ID: 1400069
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Management of inherited von Willebrand disease in 2007.
    Federici AB; Mannucci PM
    Ann Med; 2007; 39(5):346-58. PubMed ID: 17701477
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.