-
1
-
-
0023164845
-
Epidemiological investigation of the prevalence of von Willebrand's disease
-
Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand's disease. Blood. 1987;69:454-459.
-
(1987)
Blood
, vol.69
, pp. 454-459
-
-
Rodeghiero, F.1
Castaman, G.2
Dini, E.3
-
2
-
-
0027458101
-
Prevalence of von Willebrand disease in children: A multi-ethnic study
-
Werner EJ, Broxson EH, Tucker EL, Giroux DS, Shults J, Abshire TC. Prevalence of von Willebrand disease in children: a multi-ethnic study. J Pediatr. 1993;123:893-898.
-
(1993)
J Pediatr
, vol.123
, pp. 893-898
-
-
Werner, E.J.1
Broxson, E.H.2
Tucker, E.L.3
Giroux, D.S.4
Shults, J.5
Abshire, T.C.6
-
3
-
-
0025800521
-
Von Willebrand factor: Clinical features of inherited and acquired disorders
-
Bloom AL. Von Willebrand factor: clinical features of inherited and acquired disorders. Mayo Clin Proc. 1991;66:743-751.
-
(1991)
Mayo Clin Proc
, vol.66
, pp. 743-751
-
-
Bloom, A.L.1
-
4
-
-
0024331438
-
Structure of the gene for human von Willebrand factor
-
Mancuso DJ, Tuley EA, Westfield LA, et al. Structure of the gene for human von Willebrand factor. J Biol Chem. 1989;264:19514-19527.
-
(1989)
J Biol Chem
, vol.264
, pp. 19514-19527
-
-
Mancuso, D.J.1
Tuley, E.A.2
Westfield, L.A.3
-
5
-
-
0026011654
-
Human von Willebrand factor gene and pseudogene: Structural analysis and differentiation by polymerase chain reaction
-
Mancuso DJ, Tuley EA, Westfield LA, et al. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction. Biochem. 1991;30:253-269.
-
(1991)
Biochem
, vol.30
, pp. 253-269
-
-
Mancuso, D.J.1
Tuley, E.A.2
Westfield, L.A.3
-
6
-
-
0010624078
-
-
Ginsburg D, Sadler JE. von Willebrand Factor (VWF) database. http://mmg2. im.med.umich.edu/vWF/. Accessed May 16, 2001.
-
(2001)
-
-
Ginsburg, D.1
Sadler, J.E.2
-
7
-
-
0027500241
-
Von Willebrand disease: A database of point mutations, insertions and deletions
-
Ginsburg D, Sadler JE. Von Willebrand disease: a database of point mutations, insertions and deletions. Thromb Haemost. 1993;69:177-191.
-
(1993)
Thromb Haemost
, vol.69
, pp. 177-191
-
-
Ginsburg, D.1
Sadler, J.E.2
-
8
-
-
0026716153
-
Molecular genetics of von Willebrand disease
-
Ginsburg D, Bowie EJW. Molecular genetics of von Willebrand disease. Blood. 1992;79:2507-2519.
-
(1992)
Blood
, vol.79
, pp. 2507-2519
-
-
Ginsburg, D.1
Bowie, E.J.W.2
-
9
-
-
0026605718
-
Von Willebrand disease masquerading as haemophilia A
-
Mazurier C. von Willebrand disease masquerading as haemophilia A. Thromb Haemost. 1992;67:391-396.
-
(1992)
Thromb Haemost
, vol.67
, pp. 391-396
-
-
Mazurier, C.1
-
10
-
-
0028027430
-
Genetic heterogeneity of severe von Willebrand disease type III in the German population
-
Schneppenheim R, Krey S, Bergmann F, et al. Genetic heterogeneity of severe von Willebrand disease type III in the German population. Hum Genet. 1994;94:640-652.
-
(1994)
Hum Genet
, vol.94
, pp. 640-652
-
-
Schneppenheim, R.1
Krey, S.2
Bergmann, F.3
-
11
-
-
0028321794
-
Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin
-
Zhang ZP, Blomback M, Egberg N, Falk G, Anvret M, Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin. Genomics. 1994;21:188-193.
-
(1994)
Genomics
, vol.21
, pp. 188-193
-
-
Zhang, Z.P.1
Blomback, M.2
Egberg, N.3
Falk, G.4
Anvret, M.5
-
12
-
-
0026640029
-
Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I
-
Zhang ZP, Lindstedt M, Falk G, Blomback M, Egberg N, Anvret M. Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I. Am J Hum Genet. 1992;51:850-858.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 850-858
-
-
Zhang, Z.P.1
Lindstedt, M.2
Falk, G.3
Blomback, M.4
Egberg, N.5
Anvret, M.6
-
13
-
-
0000658399
-
Screening for candidate mutations causing von Willebrand's disease (vWd)
-
DJ Perry, KJ Pasi, eds. Totowa, NJ: Humana Press
-
Jenkins PV. Screening for candidate mutations causing von Willebrand's disease (vWd). In: DJ Perry, KJ Pasi, eds. Methods of Molecular Medicine: Hemostasis and Thrombosis Protocols. Totowa, NJ: Humana Press; 1999:169-177.
-
(1999)
Methods of Molecular Medicine: Hemostasis and Thrombosis Protocols
, pp. 169-177
-
-
Jenkins, P.V.1
-
14
-
-
0019795095
-
Chi, a protomer of generalized recombination in X phage, is present in immunoglobulin genes
-
Kenter AL, Birshtein BK, Chi, a protomer of generalized recombination in X phage, is present in immunoglobulin genes. Nature. 1981;293:402-404.
-
(1981)
Nature
, vol.293
, pp. 402-404
-
-
Kenter, A.L.1
Birshtein, B.K.2
-
15
-
-
0028345761
-
Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence
-
Eikenboom JCJ, Vink T, Briet E, Sixma JJ, Reitsma PH. Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence. Proc Natl Acad Sci U S A. 1994;91:2221-2224.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 2221-2224
-
-
Eikenboom, J.C.J.1
Vink, T.2
Briet, E.3
Sixma, J.J.4
Reitsma, P.H.5
-
16
-
-
0027185452
-
Mutations of von Willebrand factor gene in families with von Willebrand disease in the Äland Islands
-
Zhang ZP, Blomback M, Nyman D, Anvret M. Mutations of von Willebrand factor gene in families with von Willebrand disease in the Äland Islands. Proc Natl Acad Sci U S A. 1993;90:7937-7940.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 7937-7940
-
-
Zhang, Z.P.1
Blomback, M.2
Nyman, D.3
Anvret, M.4
-
17
-
-
0031957351
-
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin
-
Eikenboom JCJ, Castaman G, Hans LV, Rogier MB, Rodeghiero F, Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin. Thromb Haemost. 1998;79:709-717.
-
(1998)
Thromb Haemost
, vol.79
, pp. 709-717
-
-
Eikenboom, J.C.J.1
Castaman, G.2
Hans, L.V.3
Rogier, M.B.4
Rodeghiero, F.5
-
18
-
-
0034533212
-
Q1311X: A novel nonsense mutation of putative ancient origin in the von Willebrand factor gene
-
Casana P, Francisco M, Haya S, Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor gene. Br J Haematol 2000;111:552-555.
-
(2000)
Br J Haematol
, vol.111
, pp. 552-555
-
-
Casana, P.1
Francisco, M.2
Haya, S.3
-
19
-
-
0027258360
-
Von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure
-
Holmberg L, Dent JA, Schneppenheim R, Budde U, Ware J, Ruggeri ZM. Von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure. J Clin Invest. 1993;91:2169-2177.
-
(1993)
J Clin Invest
, vol.91
, pp. 2169-2177
-
-
Holmberg, L.1
Dent, J.A.2
Schneppenheim, R.3
Budde, U.4
Ware, J.5
Ruggeri, Z.M.6
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