VOn Willebrand factor fragment in type IIA von Willebrand's disease: demonstration of two different forms of fragmentsTAKAHASHI, H; TSUKADA, T; TATEWAKI, W et al.Haemostasis. 1987, Vol 17, Num 4, pp 182-188, issn 0301-0147Article

Von Willebrand factor and von Willebrand diseaseRUGGERI, Z. M; ZIMMERMAN, T. S.Blood. 1987, Vol 70, Num 4, pp 895-904, issn 0006-4971Article

Von Willebrand factor multimer patterns in von Willebrand's diseaseHOYER, L. W; RIZZA, C. R; TUDDENHAM, E. G. D et al.British journal of haematology. 1983, Vol 55, Num 3, pp 493-507, issn 0007-1048Article

Correlation between circulatin levels of von Willebrands antigen II and von Willebrand factor: discrimination between type I and type II von Willebrands diseaseMCCARROLL, D. R; RUGGERI, Z. M; MONTGOMERY, R. R et al.The Journal of laboratory and clinical medicine. 1984, Vol 103, Num 5, pp 704-711, issn 0022-2143Article

Further studies on aggregation of platelet-type von Willebrand's disease platelets by human von Willebrand factorTAKAHASHI, H; TATEWAKI, W; HANANO, M et al.Thrombosis and haemostasis. 1986, Vol 55, Num 3, pp 338-341, issn 0340-6245Article

ADAMTS-13 activity in von willebrand diseasePERUTELLI, Paolo; AMATO, Stefano; MOLINARI, Angelo C et al.Thrombosis research. 2006, Vol 117, Num 6, pp 685-688, issn 0049-3848, 4 p.Article

The effect of ABO blood group on the diagnosis of von Willebrand diseaseGILL, J. C; ENDRES-BROOKS, J; BAUER, P. J et al.Blood. 1987, Vol 69, Num 6, pp 1691-1695, issn 0006-4971Article

Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearanceCASTAMAN, Giancarlo; TOSETTO, Alberto; FEDERICI, Augusto B et al.Thrombosis and haemostasis. 2011, Vol 105, Num 4, pp 647-654, issn 0340-6245, 8 p.Article

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 diseaseSZTUKOWSKA, M; GALLINARO, L; CATTINI, M. G et al.British journal of haematology. 2008, Vol 143, Num 1, pp 107-114, issn 0007-1048, 8 p.Article

Genetics of type 1 von willebrand diseaseGOODEVE, Anne.Current opinion in hematology. 2007, Vol 14, Num 5, pp 444-449, issn 1065-6251, 6 p.Article

Evidence that calpains and elastase do not produce the von Willebrand factor fragments present in normal plasma and IIA von Willebrand diseaseBERKOWITZ, S. D; NOZAKI, H; TITANI, K et al.Blood. 1988, Vol 72, Num 2, pp 721-727, issn 0006-4971Article

Acquired von Willebrand's syndrome due to an inhibitor of IgG specific for von Willebrand's factor in polycythemia rubra veraMOHRI, H; OHKUBO, T.Acta haematologica. 1987, Vol 78, Num 4, pp 258-264, issn 0001-5792Article

In vivo experiments indicate that relatively high platelet deposition in von Willebrand's disease vicenz is caused by normal platelet-VWF level rather than by high VWF-multimers in plasmaD'ALESSIO, P. A; CASTAMAN, G; RODEGHIERO, F et al.Thrombosis research. 1992, Vol 65, Num 2, pp 221-228, issn 0049-3848Article

Distinct abnormalities in the interaction of purified types IIA and IIB von Willebrand factor with the two platelet binding sites, glycoprotein complexes Ib-IX and IIb-IIIaDE MARCO, L; MAZZUCATO, M; DE ROIA, D et al.The Journal of clinical investigation. 1990, Vol 86, Num 3, pp 785-792, issn 0021-9738Article

Von Willebrand's variant (type II Buffalo) : thrombocytopenia after desmotressin but absence of in vitro hypersensitivity to ristocetinSWEENEY, J. D; HOERNIG, L. A; BEHRENS, A. N et al.American journal of clinical pathology. 1990, Vol 93, Num 4, pp 522-525, issn 0002-9173Article

Acquired type II von Willebrand's disease: demonstration of a complexed inhibitor of the von Willebrand factor-platelet interaction and response to treatmentGOUDEMAND, J; SAMOR, B; CARON, C et al.British journal of haematology. 1988, Vol 68, Num 2, pp 227-233, issn 0007-1048Article

Type IV von Willebrand's disease and pregnancy: comparison of analytical methods of von Willebrand and factor for classification of von Willebrand's disease subtypesTAKAHASHI, H; HAYASHI, N; SHIBATA, A et al.Thrombosis research. 1988, Vol 50, Num 3, pp 409-418, issn 0049-3848Article

Platelet von Willebrand factor: evidence for its involvement in platelet adhesion to collagenFRESSINAUD, E; BARUCH, D; ROTHSCHILD, C et al.Blood. 1987, Vol 70, Num 4, pp 1214-1217, issn 0006-4971Article

Platelet von Willebrand factor: an important determinant of the bleeding time in type I von Willebrand's diseaseGRALNICK, H. R; RICK, M. E; MCKEOWN, L. P et al.Blood. 1986, Vol 68, Num 1, pp 58-61, issn 0006-4971Article

Spontaneous platelet aggregation in type IIB tampa von Willebrand disease is inhibited by the 52/48-KDA fragment of normal von Willebrand factor, which contains the GPIb binding domainSABA, H. I; FUJIMURA, Y; SABA, S. R et al.American journal of hematology. 1989, Vol 30, Num 3, pp 150-153, issn 0361-8609Article

Von Willebrand factor and von Willebrand's disease: a complex protein and a complex diseaseBONA, R. D.Annals of clinical and laboratory science. 1989, Vol 19, Num 3, pp 184-189, issn 0091-7370Article

Improved characterization of plasma von Willebrand factor heterogeneity when using 2.5% agarose gel electrophoresisMAZURIER, C; SAMOR, B; GOUDEMAND, M et al.Thrombosis and haemostasis. 1986, Vol 55, Num 1, pp 61-64, issn 0340-6245Article

Le facteur Willebrand = The Willebrand factorLARRIEU, M. J.sd, pagination multReport

Laboratory diagnostic approach of the parents―children relationship in differentiating low-level von Willebrand factor from mild type 1 von Willebrand diseaseAKIN, Mehmet.Blood coagulation & fibrinolysis. 2012, Vol 23, Num 4, pp 351-353, issn 0957-5235, 3 p.Article

Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor geneHILBERT, L; JORIEUX, S; FONTENAY-ROUPIE, M et al.British journal of haematology. 2004, Vol 127, Num 2, pp 184-189, issn 0007-1048, 6 p.Article