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kw.\*:("von 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

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

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

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

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

A short history of diagnostic tests for von willebrand disease : In memory of barry firkin (1930 to 2001) and ted zimmerman (1937 to 1988)KOUTTS, Jerry.Seminars in thrombosis and hemostasis. 2006, Vol 32, Num 5, pp 445-455, issn 0094-6176, 11 p.Article

Diagnosis and Management of von Willebrand Disease in IranCOHAN, Nader; KARIMI, Mehran.Seminars in thrombosis and hemostasis. 2011, Vol 37, Num 5, pp 602-606, issn 0094-6176, 5 p.Article

Novel evaluation method for densitometric curves of von Willebrand Factor multimers and a new parameter (MMW) to describe the degree of multimersationUDVARDY, Miklós L; SZEKERES-CSIKI, Katalin; HARSFALVI, Jolan et al.Thrombosis and haemostasis. 2009, Vol 102, Num 2, pp 412-417, issn 0340-6245, 6 p.Article

ACQUIRED VON WILLEBRAND'S SYNDROMEHOLLAND L; ADAMSON A; INGRAM GIC et al.1980; BRIT. J. HAEMATOL.; GBR; DA. 1980; VOL. 45; NO 1; PP. 161-164; BIBL. 9 REF.Article

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

CONCEPTO ACTUAL DE LA ENFERMEDAD DE VON WILLEBRAND = MALADIE DE WILLEBRANDLOPEZ BORRASCA A; VICENTE V; ALBERCA I et al.1978; SANGRE; ESP; DA. 1978; VOL. 23; NO 5B; PP. 708-727; ABS. ENG; BIBL. 58 REF.Article

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