250 related articles for article (PubMed ID: 6816083)
1. Von Willebrand's disease with thrombocytopenia, platelet function defect, and an abnormal Factor VIII molecule.
Arkel YS; Desposito F
Am J Pediatr Hematol Oncol; 1982; 4(3):249-57. PubMed ID: 6816083
[TBL] [Abstract][Full Text] [Related]
2. Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.
Weiss HJ; Hoyer LW; Rickles FR; Varma A; Rogers J
J Clin Invest; 1973 Nov; 52(11):2708-16. PubMed ID: 4542944
[TBL] [Abstract][Full Text] [Related]
3. [High-shear force-induced platelet aggregation in the screening and diagnosis of von Willebrand disease].
Schlammadinger A; Kerényi A; Muszbek L; Boda Z
Orv Hetil; 2000 Oct; 141(41):2245-50. PubMed ID: 11184249
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Defective ristocetin-induced platelet aggregation in von Willebrand's disease and its correction by factor VIII.
Weiss HJ; Rogers J; Brand H
J Clin Invest; 1973 Nov; 52(11):2697-707. PubMed ID: 4201262
[TBL] [Abstract][Full Text] [Related]
6. Studies of the human factor VIII/von Willebrand factor protein. III. Qualitative defects in von Willebrand's disease.
Gralnick HR; Coller BS; Sultan Y
J Clin Invest; 1975 Oct; 56(4):814-27. PubMed ID: 1080491
[TBL] [Abstract][Full Text] [Related]
7. Studies on the prolonged bleeding time in von Willebrand's disease.
Mannucci PM; Pareti FI; Holmberg L; Nilsson IM; Ruggeri ZM
J Lab Clin Med; 1976 Oct; 88(4):662-71. PubMed ID: 787458
[TBL] [Abstract][Full Text] [Related]
8. 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; 121(2-3):119-27. PubMed ID: 19506358
[TBL] [Abstract][Full Text] [Related]
9. Electrophoretic heterogeneity of normal factor VIII/Von Willebrand protein, and abnormal electrophoretic mobility in patients with Von Willebrand's disease.
Sultan Y; Simeon J; Caen JP
J Lab Clin Med; 1976 Feb; 87(2):185-94. PubMed ID: 1082003
[TBL] [Abstract][Full Text] [Related]
10. 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
[TBL] [Abstract][Full Text] [Related]
11. Von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment.
Castaman G; Federici AB; Rodeghiero F; Mannucci PM
Haematologica; 2003 Jan; 88(1):94-108. PubMed ID: 12551832
[TBL] [Abstract][Full Text] [Related]
12. A new variant of von Willebrand's disease (type I Padua): doublet-organized plasma von Willebrand factor oligomers in the presence of all size multimers.
Casonato A; Pontara E; Dannhäuser D; Bertomoro A; Sartori MT; Girolami A
Haematologia (Budap); 1994; 26(2):97-109. PubMed ID: 7890268
[TBL] [Abstract][Full Text] [Related]
13. Platelet interaction with vessel wall and collagen in pigs with homozygous von Willebrand's disease associated with abnormal collagen aggregation.
Badimon L; Badimon JJ; Galvez A; Turitto V; Fuster V
Thromb Haemost; 1989 Feb; 61(1):57-64. PubMed ID: 2665168
[TBL] [Abstract][Full Text] [Related]
14. 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
[TBL] [Abstract][Full Text] [Related]
15. 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
[TBL] [Abstract][Full Text] [Related]
16. Laboratory assessment as a critical component of the appropriate diagnosis and sub-classification of von Willebrand's disease.
Favaloro EJ
Blood Rev; 1999 Dec; 13(4):185-204. PubMed ID: 10741895
[TBL] [Abstract][Full Text] [Related]
17. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders.
Gupta PK; Charan VD; Saxena R
Ann Hematol; 2007 Jun; 86(6):403-7. PubMed ID: 17375300
[TBL] [Abstract][Full Text] [Related]
18. [The laboratory diagnosis of von Willebrand's disease (author's transl)].
Niessner H
Wien Klin Wochenschr; 1976 Apr; 88(7):221-31. PubMed ID: 1086551
[TBL] [Abstract][Full Text] [Related]
19. An atypical von Willebrand's disease with hyperreactivity of platelet aggregation.
Niiya K; Kubonishi I; Taguchi H; Miyoshi I
Acta Haematol; 1984; 71(3):158-64. PubMed ID: 6424380
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
