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.
153 related articles for article (PubMed ID: 19407316)
1. Clinical and laboratory versus molecular markers for a correct classification of von Willebrand disease. Federici AB; Canciani MT Haematologica; 2009 May; 94(5):610-5. PubMed ID: 19407316 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Molecular genetics of von Willebrand disease. Mazurier C; Ribba AS; Gaucher C; Meyer D Ann Genet; 1998; 41(1):34-43. PubMed ID: 9599650 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. Genotype-phenotype correlation in a cohort of Portuguese patients comprising the entire spectrum of VWD types: impact of NGS. Fidalgo T; Salvado R; Corrales I; Pinto SC; Borràs N; Oliveira A; Martinho P; Ferreira G; Almeida H; Oliveira C; Marques D; Gonçalves E; Diniz M; Antunes M; Tavares A; Caetano G; Kjöllerström P; Maia R; Sevivas TS; Vidal F; Ribeiro L Thromb Haemost; 2016 Jul; 116(1):17-31. PubMed ID: 26988807 [TBL] [Abstract][Full Text] [Related]
12. Type 2M:Milwaukee-1 von Willebrand disease: an in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets. Mancuso DJ; Kroner PA; Christopherson PA; Vokac EA; Gill JC; Montgomery RR Blood; 1996 Oct; 88(7):2559-68. PubMed ID: 8839848 [TBL] [Abstract][Full Text] [Related]
13. Laboratory Testing for Von Willebrand Factor Multimers. Oliver S; Lau KKE; Chapman K; Favaloro EJ Methods Mol Biol; 2017; 1646():495-511. PubMed ID: 28804850 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. von Willebrand disease, type 2B: A diagnosis more elusive than previously thought. Favaloro EJ Thromb Haemost; 2008 Mar; 99(3):630-1; author reply 632-3. PubMed ID: 18327414 [No Abstract] [Full Text] [Related]