-
1
-
-
77954466579
-
Accelerated clearance alone explains ultralarge multimers in VWD vicenza
-
Gezsi A, Budde U, Deak I, Nagy E, Mohl A, Schlammadinger A, Boda Z, Masszi T, Sadler JE, Bodo I. Accelerated clearance alone explains ultralarge multimers in VWD vicenza. J Thromb Haemost 2010, 8:1273-80.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 1273-1280
-
-
Gezsi, A.1
Budde, U.2
Deak, I.3
Nagy, E.4
Mohl, A.5
Schlammadinger, A.6
Boda, Z.7
Masszi, T.8
Sadler, J.E.9
Bodo, I.10
-
2
-
-
0023852791
-
Von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimers
-
Mannucci PM, Lombardi R, Castaman G, Dent JA, Lattuada A, Rodeghiero F, Zimmerman TS. von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimers. Blood 1988, 71:65-70.
-
(1988)
Blood
, vol.71
, pp. 65-70
-
-
Mannucci, P.M.1
Lombardi, R.2
Castaman, G.3
Dent, J.A.4
Lattuada, A.5
Rodeghiero, F.6
Zimmerman, T.S.7
-
3
-
-
0036095699
-
Reduced von Willebrand factor survival in type Vicenza von Willebrand disease
-
Casonato A, Pontara E, Sartorello F, Cattini MG, Sartori MT, Padrini R, Girolami A. Reduced von Willebrand factor survival in type Vicenza von Willebrand disease. Blood 2002, 99:180-4.
-
(2002)
Blood
, vol.99
, pp. 180-184
-
-
Casonato, A.1
Pontara, E.2
Sartorello, F.3
Cattini, M.G.4
Sartori, M.T.5
Padrini, R.6
Girolami, A.7
-
4
-
-
31944432453
-
Identifying type Vicenza von Willebrand disease
-
Casonato A, Pontara E, Sartorello F, Cattini MG, Gallinaro L, Bertomoro A, Rosato A, Padrini R, Pagnan A. Identifying type Vicenza von Willebrand disease. J Lab Clin Med 2006, 147:96-102.
-
(2006)
J Lab Clin Med
, vol.147
, pp. 96-102
-
-
Casonato, A.1
Pontara, E.2
Sartorello, F.3
Cattini, M.G.4
Gallinaro, L.5
Bertomoro, A.6
Rosato, A.7
Padrini, R.8
Pagnan, A.9
-
5
-
-
0033971892
-
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 families
-
Schneppenheim R, Federici AB, Budde U, Castaman G, Drewke E, Krey S, Mannucci PM, Riesen G, Rodeghiero F, Zieger B, Zimmermann R. Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 families. Thromb Haemost 2000, 83:136-40.
-
(2000)
Thromb Haemost
, vol.83
, pp. 136-140
-
-
Schneppenheim, R.1
Federici, A.B.2
Budde, U.3
Castaman, G.4
Drewke, E.5
Krey, S.6
Mannucci, P.M.7
Riesen, G.8
Rodeghiero, F.9
Zieger, B.10
Zimmermann, R.11
-
6
-
-
0033865397
-
An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutation
-
Castaman G, Missiaglia E, Federici AB, Schneppenheim R, Rodeghiero F. An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutation. Thromb Haemost 2000, 84:350-1.
-
(2000)
Thromb Haemost
, vol.84
, pp. 350-351
-
-
Castaman, G.1
Missiaglia, E.2
Federici, A.B.3
Schneppenheim, R.4
Rodeghiero, F.5
-
7
-
-
33746988071
-
Von Willebrand's disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency
-
Casana P, Cabrera N, Haya S, Cid AR, Aznar JA. Von Willebrand's disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency. Haematologica 2006, 91:1130-3.
-
(2006)
Haematologica
, vol.91
, pp. 1130-1133
-
-
Casana, P.1
Cabrera, N.2
Haya, S.3
Cid, A.R.4
Aznar, J.A.5
-
8
-
-
43149115418
-
Re-evaluation of three Israeli families initially diagnosed with type 1 von Willebrand disease in light of the ISTH update on von Willebrand factor pathophysiology and classification
-
Hashemi Soteh SM, Anson J, Inbal A, Peake IR, Goodeve AC. Re-evaluation of three Israeli families initially diagnosed with type 1 von Willebrand disease in light of the ISTH update on von Willebrand factor pathophysiology and classification. Haemophilia 2008, 14:621-4.
-
(2008)
Haemophilia
, vol.14
, pp. 621-624
-
-
Hashemi Soteh, S.M.1
Anson, J.2
Inbal, A.3
Peake, I.R.4
Goodeve, A.C.5
-
9
-
-
25744466348
-
Inherited and de novo von Willebrand disease 'Vicenza' in UK families with the R1205H mutation
-
Lester WA, Guilliatt AM, Surdhar GK, Enayat MS, Hill FGH. Inherited and de novo von Willebrand disease 'Vicenza' in UK families with the R1205H mutation. J Thromb Haemost 2003, (Supplement).
-
(2003)
J Thromb Haemost
, Issue.SUPPL.
-
-
Lester, W.A.1
Guilliatt, A.M.2
Surdhar, G.K.3
Enayat, M.S.4
Hill, F.G.H.5
-
10
-
-
33751219230
-
An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease
-
Cumming A, Grundy P, Keeney S, Lester W, Enayat S, Guilliatt A, Bowen D, Pasi J, Keeling D, Hill F, Bolton-Maggs PH, Hay C, Collins P. An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease. Thromb Haemost 2006, 96:630-41.
-
(2006)
Thromb Haemost
, vol.96
, pp. 630-641
-
-
Cumming, A.1
Grundy, P.2
Keeney, S.3
Lester, W.4
Enayat, S.5
Guilliatt, A.6
Bowen, D.7
Pasi, J.8
Keeling, D.9
Hill, F.10
Bolton-Maggs, P.H.11
Hay, C.12
Collins, P.13
-
11
-
-
33845967766
-
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
-
Goodeve A, Eikenboom J, Castaman G. Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD). Blood 2007, 109:112-21.
-
(2007)
Blood
, vol.109
, pp. 112-121
-
-
Goodeve, A.1
Eikenboom, J.2
Castaman, G.3
-
12
-
-
33846026307
-
The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study
-
James PD, Notley C, Hegadorn C, Leggo J, Tuttle A, Tinlin S, Brown C, Andrews C, Labelle A, Chirinian Y, O'Brien L, Othman M, Rivard G, Rapson D, Hough C, Lillicrap D. The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study. Blood 2007, 109:145-54.
-
(2007)
Blood
, vol.109
, pp. 145-154
-
-
James, P.D.1
Notley, C.2
Hegadorn, C.3
Leggo, J.4
Tuttle, A.5
Tinlin, S.6
Brown, C.7
Andrews, C.8
Labelle, A.9
Chirinian, Y.10
O'Brien, L.11
Othman, M.12
Rivard, G.13
Rapson, D.14
Hough, C.15
Lillicrap, D.16
-
13
-
-
52649093281
-
Macrophages contribute to the cellular uptake of von Willebrand factor and factor VIII in vivo
-
van Schooten CJ, Shahbazi S, Groot E, Oortwijn BD, van den Berg HM, Denis CV, Lenting PJ. Macrophages contribute to the cellular uptake of von Willebrand factor and factor VIII in vivo. Blood 2008, 112:1704-12.
-
(2008)
Blood
, vol.112
, pp. 1704-1712
-
-
van Schooten, C.J.1
Shahbazi, S.2
Groot, E.3
Oortwijn, B.D.4
van den Berg, H.M.5
Denis, C.V.6
Lenting, P.J.7
-
14
-
-
33746582792
-
Laboratory testing for von Willebrand disease: contribution of multimer analysis to diagnosis and classification
-
Budde U, Pieconka A, Will K, Schneppenheim R. Laboratory testing for von Willebrand disease: contribution of multimer analysis to diagnosis and classification. Semin Thromb Hemost 2006, 32:514-21.
-
(2006)
Semin Thromb Hemost
, vol.32
, pp. 514-521
-
-
Budde, U.1
Pieconka, A.2
Will, K.3
Schneppenheim, R.4
-
15
-
-
1842530336
-
An experimental model to study the in vivo survival of von Willebrand factor. Basic aspects and application to the R1205H mutation
-
Lenting PJ, Westein E, Terraube V, Ribba AS, Huizinga EG, Meyer D, de Groot PG, Denis CV. An experimental model to study the in vivo survival of von Willebrand factor. Basic aspects and application to the R1205H mutation. J Biol Chem 2004, 279:12102-9.
-
(2004)
J Biol Chem
, vol.279
, pp. 12102-12109
-
-
Lenting, P.J.1
Westein, E.2
Terraube, V.3
Ribba, A.S.4
Huizinga, E.G.5
Meyer, D.6
de Groot, P.G.7
Denis, C.V.8
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