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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
648 related items for PubMed ID: 18449422
1. Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: influence of glycosylation, proteolysis and gene mutations. Millar CM, Riddell AF, Brown SA, Starke R, Mackie I, Bowen DJ, Jenkins PV, van Mourik JA. Thromb Haemost; 2008 May; 99(5):916-24. PubMed ID: 18449422 [Abstract] [Full Text] [Related]
2. 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 May; 121(2-3):128-38. PubMed ID: 19506359 [Abstract] [Full Text] [Related]
3. Laboratory diagnosis and molecular classification of von Willebrand disease. Gadisseur A, Hermans C, Berneman Z, Schroyens W, Deckmyn H, Michiels JJ. Acta Haematol; 2009 May; 121(2-3):71-84. PubMed ID: 19506352 [Abstract] [Full Text] [Related]
4. Von Willebrand factor propeptide makes it easy to identify the shorter Von Willebrand factor survival in patients with type 1 and type Vicenza von Willebrand disease. Sztukowska M, Gallinaro L, Cattini MG, Pontara E, Sartorello F, Daidone V, Padrini R, Pagnan A, Casonato A. Br J Haematol; 2008 Oct; 143(1):107-14. PubMed ID: 18691167 [Abstract] [Full Text] [Related]
5. Dominant von Willebrand disease type 2A groups I and II due to missense mutations in the A2 domain of the von Willebrand factor gene: diagnosis and management. Michiels JJ, van Vliet HH. Acta Haematol; 2009 Oct; 121(2-3):154-66. PubMed ID: 19506362 [Abstract] [Full Text] [Related]
6. Response of von Willebrand factor parameters to desmopressin in patients with type 1 and type 2 congenital von Willebrand disease: diagnostic and therapeutic implications. Michiels JJ, van de Velde A, van Vliet HH, van der Planken M, Schroyens W, Berneman Z. Semin Thromb Hemost; 2002 Apr; 28(2):111-32. PubMed ID: 11992235 [Abstract] [Full Text] [Related]
7. Increased clearance of von Willebrand factor antigen post-DDAVP in Type 1 von Willebrand disease: is it a potential pathogenic process? Brown SA, Eldridge A, Collins PW, Bowen DJ. J Thromb Haemost; 2003 Aug; 1(8):1714-7. PubMed ID: 12911582 [Abstract] [Full Text] [Related]
10. Assessment of von Willebrand factor propeptide improves the diagnosis of von Willebrand disease. Casonato A, Daidone V, Padrini R. Semin Thromb Hemost; 2011 Jul; 37(5):456-63. PubMed ID: 22102187 [Abstract] [Full Text] [Related]
11. Intravenous DDAVP and factor VIII-von Willebrand factor concentrate for the treatment and prophylaxis of bleedings in patients With von Willebrand disease type 1, 2 and 3. Michiels JJ, van Vliet HH, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, van der Velden A, Budde U. Clin Appl Thromb Hemost; 2007 Jan; 13(1):14-34. PubMed ID: 17164493 [Abstract] [Full Text] [Related]
13. Effect of desmopressin on von Willebrand factor multimers in Doberman Pinschers with type 1 von Willebrand disease. Callan MB, Giger U, Catalfamo JL. Am J Vet Res; 2005 May; 66(5):861-7. PubMed ID: 15938072 [Abstract] [Full Text] [Related]
15. Recessive von Willebrand disease type 2 Normandy: variable expression of mild hemophilia and VWD type 1. Michiels JJ, Gadisseur A, Vangenegten I, Schroyens W, Berneman Z. Acta Haematol; 2009 May; 121(2-3):119-27. PubMed ID: 19506358 [Abstract] [Full Text] [Related]
16. 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 [Abstract] [Full Text] [Related]
17. Laboratory diagnosis of von Willebrand disorder (vWD) and monitoring of DDAVP therapy: efficacy of the PFA-100 and vWF:CBA as combined diagnostic strategies. Favaloro EJ, Kershaw G, Bukuya M, Hertzberg M, Koutts J. Haemophilia; 2001 Mar; 7(2):180-9. PubMed ID: 11260278 [Abstract] [Full Text] [Related]
18. Laboratory diagnosis and molecular basis of mild von Willebrand disease type 1. Michiels JJ, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, van Vliet HH. Acta Haematol; 2009 Mar; 121(2-3):85-97. PubMed ID: 19506353 [Abstract] [Full Text] [Related]