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kw.\*:("Willebrand disease")

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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

Severe von Willebrand's disease: SDS agarose multimer analysisREDAELLI, R; PEZZETTI, L; CAIMI, T et al.Haemostasis. 1987, Vol 17, Num 5, pp 278-285, issn 0301-0147Article

Le syndrome de Willebrand acquis: à propos de 2 observations = Acquired von Willebrand's disease: 2 casesFLECHET, B; BORG, J. Y; LEGENDRE, M et al.LARC médical. 1984, Vol 4, Num 1, pp 15-21, issn 0242-9462Article

Linkage analysis in von Willebrand diseaseVERP, M. S; RADVANY, R. M; GREEN, D et al.Clinical genetics. 1983, Vol 24, Num 6, pp 434-438, issn 0009-9163Article

Distinguishing between type 2B and pseudo-von willebrand disease and its clinical importanceENAYAT, Mohammad S; GUILLIATT, Andrea M; LESTER, William et al.British journal of haematology. 2006, Vol 133, Num 6, pp 664-666, issn 0007-1048, 3 p.Article

Von Willebrand diseaseHOLMBERG, L; NILSSON, I. M.Clinics in haematology. 1985, Vol 14, Num 2, pp 461-488, issn 0308-2261Article

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

A study of a Caucasian family with variant von Willebrand's disease in association with vascular telangiectasia and haemoglobinopathyHANNA, W; MCCARROLL, D; LIN, D et al.Thrombosis and haemostasis. 1984, Vol 51, Num 2, pp 275-278, issn 0340-6245Article

The impact of bleeding history, von Willebrand factor and PFA-100® on the diagnosis of type 1 von Willebrand disease: results from the European study MCMDM-1VWDCASTAMAN, Giancarlo; TOSETTO, Alberto; EIKENBOOM, Jeroen et al.British journal of haematology. 2010, Vol 151, Num 3, pp 245-251, issn 0007-1048, 7 p.Article

Use of a new enzyme-linked immunosorbent assay for the detection of type 2N von willebrand disease and its prevalence in an Indian populationGHOSH, Kanjaksha; TRASI, Sucheta; SHETTY, Shrimati et al.Blood coagulation & fibrinolysis. 2006, Vol 17, Num 1, pp 7-11, issn 0957-5235, 5 p.Article

Prophylaxis and treatment of bleeding complications in von willebrand disease type 3BERNTORP, Erik.Seminars in thrombosis and hemostasis. 2006, Vol 32, Num 6, pp 621-625, issn 0094-6176, 5 p.Article

Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European studyFEDERICI, Augusto B; MAZURIER, Claudine; MANNUCCI, Pier M et al.Blood. 2004, Vol 103, Num 6, pp 2032-2038, issn 0006-4971, 7 p.Article

Dépistage simple et rapide des formes frustes de la maladie de Willebrand = Easy and quick investigation of the atypical forms of Von Willebrand's diseaseMASSIGNON, D; SAUMET, M; CLERC-RENAUD, P et al.Lyon médical. 1984, Vol 251, Num 3, pp 91-93, issn 0024-7790Article

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

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

The anti-von Willebrand factor aptamer ARC1779 increases von Willebrand factor levels and platelet counts in patients with type 2B von Willebrand diseaseJILMA-STOHLAWETZ, Petra; KNÖBL, Paul; GILBERT, James C et al.Thrombosis and haemostasis. 2012, Vol 108, Num 2, pp 284-290, issn 0340-6245, 7 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

Impaired dimerization of von willebrand factor subunit due to mutation A280 ID in the CK domain results in a recessive type 2A subtype IID von willebrand diseaseHOMMAIS, Antoine; STEPANIAN, Alain; FRESSINAUD, Edith et al.Thrombosis and haemostasis. 2006, Vol 95, Num 5, pp 776-781, issn 0340-6245, 6 p.Article

Acquired von Willebrand's disease in the myeloproliferative syndromeBUDDE, U; SCHAEFER, G; MUELLER, N et al.Blood. 1984, Vol 64, Num 5, pp 981-985, issn 0006-4971Article

A variant of von Willebrand's disease characterized by recessive inheritance and missing triplet structure of von Willebrand factor multimersMANNUCCI, P. M; LOMBARDI, R; PARETI, F. I et al.Blood. 1983, Vol 62, Num 5, pp 1000-1005, issn 0006-4971Article

Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease in southern IranSHAMSAKHZARI, Shoeleh; AFRASIABI, Abdolreza; HAGHPANAH, Sezaneh et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 4, pp 325-330, issn 0957-5235, 6 p.Article

Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand diseaseSCHNEPPENHEIM, Reinhard; BUDDE, Ulrich; OBSER, Tobias et al.Blood. 2001, Vol 97, Num 7, pp 2059-2066, issn 0006-4971Article

Von Willebrand factor and platelet functionMOROOSE, R; HOYER, L. W.Annual review of medicine. 1986, Vol 37, pp 157-163, issn 0066-4219Article

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