-
2
-
-
0000636412
-
The pathogenesis of purpura hemorrhagica with special reference to the part played by blood platelets
-
Duke WW. The pathogenesis of purpura hemorrhagica with special reference to the part played by blood platelets. Arch Intern Med 1912;10:445-469
-
(1912)
Arch Intern Med
, vol.10
, pp. 445-469
-
-
Duke, W.W.1
-
3
-
-
0005092889
-
The standardization of certain factors in the cutaneous "venostasis bleeding time technique."
-
Ivy AC, Nelson D, Bucher G. The standardization of certain factors in the cutaneous "venostasis bleeding time technique." J Lab Clin Med 1941;26:1812-1822
-
(1941)
J Lab Clin Med
, vol.26
, pp. 1812-1822
-
-
Ivy, A.C.1
Nelson, D.2
Bucher, G.3
-
4
-
-
73049146910
-
The haemostatic effect of normal platelets in haemophilia and factor V deficiency
-
Borchgrevink CF. The haemostatic effect of normal platelets in haemophilia and factor V deficiency. Acta Med Scand 1961;170:378-383
-
(1961)
Acta Med Scand
, vol.170
, pp. 378-383
-
-
Borchgrevink, C.F.1
-
5
-
-
0000203483
-
Measurement of platelet adhesiveness: A simple in vitro technique demonstrating an abnormality in von Willebrand's disease
-
Salzman EW. Measurement of platelet adhesiveness: a simple in vitro technique demonstrating an abnormality in von Willebrand's disease. J Lab Clin Med 1963;62:724-735
-
(1963)
J Lab Clin Med
, vol.62
, pp. 724-735
-
-
Salzman, E.W.1
-
7
-
-
0014336050
-
Congenital bleeding disorders with long bleeding time and normal platelet count. II. Von Willebrand's disease (report of thirty seven patients)
-
Larrieu MJ, Caen JP, Meyer DO, et al. Congenital bleeding disorders with long bleeding time and normal platelet count. II. Von Willebrand's disease (report of thirty seven patients). Am J Med 1968;45:3S4-372
-
(1968)
Am J Med
, vol.45
-
-
Larrieu, M.J.1
Caen, J.P.2
Meyer, D.O.3
-
8
-
-
0025166288
-
A critical reappraisal of the bleeding time
-
Rodgers RPC, Levin J. A critical reappraisal of the bleeding time. Semin Thromb Hemost 1990;16:1-20
-
(1990)
Semin Thromb Hemost
, vol.16
, pp. 1-20
-
-
Rodgers, R.P.C.1
Levin, J.2
-
9
-
-
0025768028
-
The bleeding time does not predict surgical bleeding
-
Lind SE. The bleeding time does not predict surgical bleeding. Blood 1991;77:2547-2552
-
(1991)
Blood
, vol.77
, pp. 2547-2552
-
-
Lind, S.E.1
-
10
-
-
0015247223
-
Ristocetin: A new tool in the investigation of platelet aggregation
-
Howard MA, Firkin BG. Ristocetin: a new tool in the investigation of platelet aggregation. Thromb Diath Haemorrh 1971;26:362-369
-
(1971)
Thromb Diath Haemorrh
, vol.26
, pp. 362-369
-
-
Howard, M.A.1
Firkin, B.G.2
-
11
-
-
0015624119
-
Ristocetin: A means of differentiating von Willebrand's disease into two groups
-
Howard MA, Sawers RJ, Firkin BG. Ristocetin: a means of differentiating von Willebrand's disease into two groups. Blood 1973;41:687-690
-
(1973)
Blood
, vol.41
, pp. 687-690
-
-
Howard, M.A.1
Sawers, R.J.2
Firkin, B.G.3
-
12
-
-
0015856625
-
Quantitative assay of a plasma factor, deficient in von Willebrand's disease, that is necessary for platelet aggregation. Relationship to factor VIII pro-coagulant activity and antigen content
-
Weiss HJ, Hoyer LW, Rickles FR, et al. Quantitative assay of a plasma factor, deficient in von Willebrand's disease, that is necessary for platelet aggregation. Relationship to factor VIII pro-coagulant activity and antigen content. J Clin Invest 1973;52:2708-2716
-
(1973)
J Clin Invest
, vol.52
, pp. 2708-2716
-
-
Weiss, H.J.1
Hoyer, L.W.2
Rickles, F.R.3
-
13
-
-
0016352720
-
Von Willebrand factor and ristocetin. 1. Mechanism of ristocetin induced platelet aggregation
-
Jenkins CS, Meyer D, Dreyfus MD, et al. Von Willebrand factor and ristocetin. 1. Mechanism of ristocetin induced platelet aggregation. Br J Haematol 1974;28:561-578
-
(1974)
Br J Haematol
, vol.28
, pp. 561-578
-
-
Jenkins, C.S.1
Meyer, D.2
Dreyfus, M.D.3
-
14
-
-
0016612738
-
Evaluation of ristocetin-Willebrand factor assay and ristocetin induced platelet aggregation
-
Olson JD, Brockway WI, Fass DN. Evaluation of ristocetin-Willebrand factor assay and ristocetin induced platelet aggregation. Am J Clin Pathol 1975;63:210-218
-
(1975)
Am J Clin Pathol
, vol.63
, pp. 210-218
-
-
Olson, J.D.1
Brockway, W.I.2
Fass, D.N.3
-
15
-
-
0014976247
-
Immunological differentiation of classical hemophilia (factor VIII deficiency) and von Willebrand's disease with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and an acquired anticoagulant against antihemophilic factor
-
Zimmerman TS, Ratnoff OD, Powell AE. Immunological differentiation of classical hemophilia (factor VIII deficiency) and von Willebrand's disease with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and an acquired anticoagulant against antihemophilic factor. J Clin Invest 1971;50:244-254
-
(1971)
J Clin Invest
, vol.50
, pp. 244-254
-
-
Zimmerman, T.S.1
Ratnoff, O.D.2
Powell, A.E.3
-
16
-
-
0016782474
-
Determination of the von Willebrand's disease antigen (factor VIII related antigen) in plasma by quantitative immunoelectrophoresis
-
Zimmerman TS, Hoyer LW, Dickinson L, Edgington TS. Determination of the von Willebrand's disease antigen (factor VIII related antigen) in plasma by quantitative immunoelectrophoresis. J Lab Clin Med 1975;86:152-159
-
(1975)
J Lab Clin Med
, vol.86
, pp. 152-159
-
-
Zimmerman, T.S.1
Hoyer, L.W.2
Dickinson, L.3
Edgington, T.S.4
-
17
-
-
0017352185
-
The use of an immunoradiometric assay for FVIII related antigen in the study of atypical von Willebrand's disease
-
Peake IR, Bloom AL. The use of an immunoradiometric assay for FVIII related antigen in the study of atypical von Willebrand's disease. Thromb Res 1977;10:27-32
-
(1977)
Thromb Res
, vol.10
, pp. 27-32
-
-
Peake, I.R.1
Bloom, A.L.2
-
19
-
-
0018617698
-
Factor VIII physiology and pathology in man
-
Brown E, ed. New York: Grune and Stratton
-
Koutts J, Howard MA, Firkin BG. Factor VIII physiology and pathology in man. In: Brown E, ed. Progress in Hematology. XI. New York: Grune and Stratton; 1979:115-145
-
(1979)
Progress in Hematology. XI
, pp. 115-145
-
-
Koutts, J.1
Howard, M.A.2
Firkin, B.G.3
-
20
-
-
0023632686
-
Factor VIII/von Willebrand factor. Structure and function
-
Zimmerman TS. Factor VIII/von Willebrand factor. Structure and function. Ann NY Acad Sci 1987;509:53-59
-
(1987)
Ann NY Acad Sci
, vol.509
, pp. 53-59
-
-
Zimmerman, T.S.1
-
21
-
-
0021677942
-
Structure of human factor VIII
-
Vehar GA, Keyt B, Eaton D, et al. Structure of human factor VIII. Nature 1984;312:337-342
-
(1984)
Nature
, vol.312
, pp. 337-342
-
-
Vehar, G.A.1
Keyt, B.2
Eaton, D.3
-
22
-
-
0018855952
-
Variant von Willebrand disease: Characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets
-
Ruggeri ZM, Zimmerman TS. Variant von Willebrand disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets. J Clin Invest 1980;65:1318-1325
-
(1980)
J Clin Invest
, vol.65
, pp. 1318-1325
-
-
Ruggeri, Z.M.1
Zimmerman, T.S.2
-
23
-
-
0029858896
-
Shear dependent changes in the three dimensional structure of human von Willebrand factor
-
Siedlecki CA, Lestini J, Kottke-Marchant KK, et al. Shear dependent changes in the three dimensional structure of human von Willebrand factor. Blood 1996;88:2939-2950
-
(1996)
Blood
, vol.88
, pp. 2939-2950
-
-
Siedlecki, C.A.1
Lestini, J.2
Kottke-Marchant, K.K.3
-
24
-
-
0031018309
-
Von Willebrand factor
-
Ruggeri ZM. Von Willebrand factor. J Clin Invest 1997;99: 559-564
-
(1997)
J Clin Invest
, vol.99
, pp. 559-564
-
-
Ruggeri, Z.M.1
-
25
-
-
0021844825
-
Human von Willebrand factor (VWF): Isolation of complementary DNA (cDNA) clones and chromosomal localisation
-
Ginsburg D, Handin RI, Bonthron DT. Human von Willebrand factor (VWF): isolation of complementary DNA (cDNA) clones and chromosomal localisation. Science 1985;228:1401-1406
-
(1985)
Science
, vol.228
, pp. 1401-1406
-
-
Ginsburg, D.1
Handin, R.I.2
Bonthron, D.T.3
-
26
-
-
2442469461
-
Cloning and characterization of two cDNAs coding for human von Willebrand factor
-
Sadler JE, Shelton-Inloes BB, Sorace JM, et al. Cloning and characterization of two cDNAs coding for human von Willebrand factor. Proc Natl Acad Sci USA 1985;82:6394-6398
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 6394-6398
-
-
Sadler, J.E.1
Shelton-Inloes, B.B.2
Sorace, J.M.3
-
28
-
-
0141498240
-
Von Willebrand factor, platelets and endothelial cell interactions
-
Ruggeri ZM. Von Willebrand factor, platelets and endothelial cell interactions. J Thromb Haemost 2003;1:1335-1342
-
(2003)
J Thromb Haemost
, vol.1
, pp. 1335-1342
-
-
Ruggeri, Z.M.1
-
30
-
-
26444535506
-
GPVI and integrin alphaIIbeta3 signaling in platelets
-
Watson SP, Auger JM, McCarty OJT, et al. GPVI and integrin alphaIIbeta3 signaling in platelets. J Thromb Haemost 2005;3:1752-1762
-
(2005)
J Thromb Haemost
, vol.3
, pp. 1752-1762
-
-
Watson, S.P.1
Auger, J.M.2
McCarty, O.J.T.3
-
31
-
-
0030999134
-
Platelet GPIIb/IIIa antagonists: The first anti-integrin receptor therapeutics
-
Coller BS. Platelet GPIIb/IIIa antagonists: the first anti-integrin receptor therapeutics. J Clin Invest 1997;99:1467-1471
-
(1997)
J Clin Invest
, vol.99
, pp. 1467-1471
-
-
Coller, B.S.1
-
32
-
-
0034066977
-
Old concepts and new developments in the study of platelet aggregation
-
Ruggeri ZM. Old concepts and new developments in the study of platelet aggregation. J Clin Invest 2000;105:699-701
-
(2000)
J Clin Invest
, vol.105
, pp. 699-701
-
-
Ruggeri, Z.M.1
-
33
-
-
0021119682
-
Von Willebrand's disease from 1926-1983
-
Nilsson IM. von Willebrand's disease from 1926-1983. Scand J Haematol 1984;33(suppl 40):21-43
-
(1984)
Scand J Haematol
, vol.33
, Issue.SUPPL. 40
, pp. 21-43
-
-
Nilsson, I.M.1
-
34
-
-
1842393294
-
A familial hemorrhagic condition associated with a prolongation of the bleeding time
-
Minot G. A familial hemorrhagic condition associated with a prolongation of the bleeding time. Am J Med Sci 1928; 175:301-306
-
(1928)
Am J Med Sci
, vol.175
, pp. 301-306
-
-
Minot, G.1
-
35
-
-
0002641258
-
The assay of antihaemophilic-globulin activity
-
Biggs R, Eveling J, Richards G. The assay of antihaemophilic-globulin activity. Br J Haematol 1955;1:20-24
-
(1955)
Br J Haematol
, vol.1
, pp. 20-24
-
-
Biggs, R.1
Eveling, J.2
Richards, G.3
-
36
-
-
0001324515
-
A one stage factor VIII (antihaemophilic globulin) assay and its use on venous and capillary plasma
-
Hardisty RM, Macpherson JC. A one stage factor VIII (antihaemophilic globulin) assay and its use on venous and capillary plasma. Thromb Death Haemorrh 1962;7:215-228
-
(1962)
Thromb Death Haemorrh
, vol.7
, pp. 215-228
-
-
Hardisty, R.M.1
Macpherson, J.C.2
-
37
-
-
0342665073
-
Dual hemostatic defect in pseudohemophilia
-
abst
-
Alexander B, Goldstein R. Dual hemostatic defect in pseudohemophilia. J Clin Invest 1953;32:551 (abst)
-
(1953)
J Clin Invest
, vol.32
, pp. 551
-
-
Alexander, B.1
Goldstein, R.2
-
38
-
-
0002857544
-
On an inherited autosomal haemorrhagic diathesis with antihaemophilic globulin (AHG) deficiency and prolonged bleeding time
-
Nilsson IM, Blombäck M, von Fränckel I. On an inherited autosomal haemorrhagic diathesis with antihaemophilic globulin (AHG) deficiency and prolonged bleeding time. Acta Med Scand 1957;159:35-37
-
(1957)
Acta Med Scand
, vol.159
, pp. 35-37
-
-
Nilsson, I.M.1
Blombäck, M.2
Von Fränckel, I.3
-
39
-
-
77049263615
-
Vascular hemophilia. A familial hemorrhagic disease in males and females characterized by combined antihemophilic globulin deficiency and vascular abnormalities
-
Shulman J, Smith CH, Erlandson M, et al. Vascular hemophilia. A familial hemorrhagic disease in males and females characterized by combined antihemophilic globulin deficiency and vascular abnormalities. Pediatrics 1956;18: 347-361
-
(1956)
Pediatrics
, vol.18
, pp. 347-361
-
-
Shulman, J.1
Smith, C.H.2
Erlandson, M.3
-
40
-
-
33746608425
-
Antihaemorphilic factor deficiency: Capillary defects of von Willebrand type, and idiopathic thrombocytopenia occurring in one family
-
Blackburn EK, Macfie JM, Monaghan JH, Page AP. Antihaemorphilic factor deficiency: capillary defects of von Willebrand type, and idiopathic thrombocytopenia occurring in one family. J Clin Path 1961;14:540-542
-
(1961)
J Clin Path
, vol.14
, pp. 540-542
-
-
Blackburn, E.K.1
Macfie, J.M.2
Monaghan, J.H.3
Page, A.P.4
-
41
-
-
0001164136
-
Willebrand's disease in Sweden. Its pathogenesis and treatment
-
Nilsson IM, Blombäck M, von Blombäck B. Willebrand's disease in Sweden. Its pathogenesis and treatment. Acta Med Scand 1959;164:263-278
-
(1959)
Acta Med Scand
, vol.164
, pp. 263-278
-
-
Nilsson, I.M.1
Blombäck, M.2
Von Blombäck, B.3
-
42
-
-
0001536999
-
Transfusion studies in von Willebrand's disease: Effect on bleeding time and factor VIII
-
Cornu P, Larrieu MJ, Caen J, et al. Transfusion studies in von Willebrand's disease: effect on bleeding time and factor VIII. Br J Haematol 1963;9:189-202
-
(1963)
Br J Haematol
, vol.9
, pp. 189-202
-
-
Cornu, P.1
Larrieu, M.J.2
Caen, J.3
-
43
-
-
0018779080
-
Genetics of classic von Willebrand's disease. 1. Phenotypic variations within families
-
Miller CH, Graham JB, Goldin LR, et al. Genetics of classic von Willebrand's disease. 1. Phenotypic variations within families. Blood 1979;54:117-136
-
(1979)
Blood
, vol.54
, pp. 117-136
-
-
Miller, C.H.1
Graham, J.B.2
Goldin, L.R.3
-
44
-
-
0018974968
-
Serial studies in von Willebrand's disease: Variability versus "variants"
-
Abildgaard CF, Suzuki Z, Harrison J, et al. Serial studies in von Willebrand's disease: variability versus "variants". Blood 1980;56:712-716
-
(1980)
Blood
, vol.56
, pp. 712-716
-
-
Abildgaard, C.F.1
Suzuki, Z.2
Harrison, J.3
-
45
-
-
33746592809
-
Aggregation of blood platelets by adenosine diphosphate and its reversal
-
Born GVR. Aggregation of blood platelets by adenosine diphosphate and its reversal. Nature 1982;194:827-829
-
(1982)
Nature
, vol.194
, pp. 827-829
-
-
Born, G.V.R.1
-
46
-
-
58049112386
-
Ristocetin, antimicrobial properties
-
Grundy WE, Sinclair AC, Theriault RJ, et al. Ristocetin, antimicrobial properties. Antibiotics Ann 1956-7;1:687-698
-
(1956)
Antibiotics Ann
, vol.1
, pp. 687-698
-
-
Grundy, W.E.1
Sinclair, A.C.2
Theriault, R.J.3
-
47
-
-
0013627458
-
Complications of ristocetin therapy
-
Gangarosa EJ. Complications of ristocetin therapy. Lancet 1958;1:1179-1180
-
(1958)
Lancet
, vol.1
, pp. 1179-1180
-
-
Gangarosa, E.J.1
-
48
-
-
33746640387
-
Ristocetin - A statistical review of 333 cases
-
Herting RJ, Lees B, Zimmerman AJ, et al. Ristocetin-a statistical review of 333 cases. JAMA 1956-7;1:687-698
-
(1956)
JAMA
, vol.1
, pp. 687-698
-
-
Herting, R.J.1
Lees, B.2
Zimmerman, A.J.3
-
49
-
-
0015520498
-
Qualitative platelet abnormalities in idiopathic thrombocytopaenic purpure
-
Clancy RL, Jenkins E, Firkin B. Qualitative platelet abnormalities in idiopathic thrombocytopaenic purpure. N Engl J Med 1972;286:622-626
-
(1972)
N Engl J Med
, vol.286
, pp. 622-626
-
-
Clancy, R.L.1
Jenkins, E.2
Firkin, B.3
-
50
-
-
0015220356
-
Platelet defects in infectious mononucleosis
-
Clancy R, Jenkins E, Firkin B. Platelet defects in infectious mononucleosis. BMJ 1971;4:646-648
-
(1971)
BMJ
, vol.4
, pp. 646-648
-
-
Clancy, R.1
Jenkins, E.2
Firkin, B.3
-
51
-
-
0015429926
-
Qualitative platelet defects with reduced life span in acute leukaemia
-
Van der Weyden MB, Clancy RL, Howard MA, et al. Qualitative platelet defects with reduced life span in acute leukaemia. Aust N Z J Med 1972;4:339-345
-
(1972)
Aust N Z J Med
, vol.4
, pp. 339-345
-
-
Van Der Weyden, M.B.1
Clancy, R.L.2
Howard, M.A.3
-
52
-
-
0015918491
-
Hereditary giant platelet syndrome: A disorder of a new aspect of platelet function
-
Howard MA, Hutton RA, Hardisty RM. Hereditary giant platelet syndrome: a disorder of a new aspect of platelet function. Br Med J 1973;2:586-588
-
(1973)
Br Med J
, vol.2
, pp. 586-588
-
-
Howard, M.A.1
Hutton, R.A.2
Hardisty, R.M.3
-
53
-
-
0028201807
-
A revised classification of von Willebrand disease
-
Sadler JE. for the Subcommittee on von Willebrand Factor of the Scientific and Standardisation Committee of the International Society on Thrombosis and Haemostasis. A revised classification of von Willebrand disease. Thromb Haemost 1994;71:520-525
-
(1994)
Thromb Haemost
, vol.71
, pp. 520-525
-
-
Sadler, J.E.1
-
54
-
-
0017334854
-
Spectrum of von Willebrand's disease. A study of 100 cases
-
Italian Working Group. Spectrum of von Willebrand's disease. A study of 100 cases. Br J Haematol 1977;35:101-112
-
(1977)
Br J Haematol
, vol.35
, pp. 101-112
-
-
-
55
-
-
0018871618
-
Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease
-
Ruggeri ZM, Pareti FI, Mannucci PM, et al. Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease. N Engl J Med 1980;302:1047-1051
-
(1980)
N Engl J Med
, vol.302
, pp. 1047-1051
-
-
Ruggeri, Z.M.1
Pareti, F.I.2
Mannucci, P.M.3
-
56
-
-
0025727370
-
Identification of a point mutation in type IIb von Willebrand disease illustrating the regulation of von Willebrand factor affinity for the platelet membrane glycoprotein Ib-IX receptor
-
Ware J, Dent JA, Azuma H, et al. Identification of a point mutation in type IIb von Willebrand disease illustrating the regulation of von Willebrand factor affinity for the platelet membrane glycoprotein Ib-IX receptor. Proc Natl Acad Sci USA 1991;88:2946-2950
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 2946-2950
-
-
Ware, J.1
Dent, J.A.2
Azuma, H.3
-
57
-
-
0025732427
-
Molecular basis of von Willebrand disease type IIB
-
Randi AM, Rabinowitz I, Mancuso DJ, et al. Molecular basis of von Willebrand disease type IIB. J Clin Invest 1991;87: 1220-1226
-
(1991)
J Clin Invest
, vol.87
, pp. 1220-1226
-
-
Randi, A.M.1
Rabinowitz, I.2
Mancuso, D.J.3
-
58
-
-
0025869633
-
The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding sequence
-
Cooney KA, Nichols WC, Bruck ME, et al. The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding sequence. J Clin Invest 1991; 87:1227-1233
-
(1991)
J Clin Invest
, vol.87
, pp. 1227-1233
-
-
Cooney, K.A.1
Nichols, W.C.2
Bruck, M.E.3
-
59
-
-
0019214734
-
Studies in the pathophysiology and treatment of von Willebrand's disease. IV. Mechanisms of increased ristocetin induced platelet aggregation in von Willebrand's disease
-
Takahashi H. Studies in the pathophysiology and treatment of von Willebrand's disease. IV. Mechanisms of increased ristocetin induced platelet aggregation in von Willebrand's disease. Thromb Res 1980;19:857-867
-
(1980)
Thromb Res
, vol.19
, pp. 857-867
-
-
Takahashi, H.1
-
60
-
-
0019998246
-
Platelet type von Willebrand's disease: Characterization of a new bleeding disorder
-
Miller JI, Castella A. Platelet type von Willebrand's disease: characterization of a new bleeding disorder. Blood 1982;60: 790-794
-
(1982)
Blood
, vol.60
, pp. 790-794
-
-
Miller, J.I.1
Castella, A.2
-
61
-
-
0020068005
-
Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced absorbtion of its high molecular weight multimers
-
Weiss HJ, Meyer D, Rabinowitz R, et al. Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced absorbtion of its high molecular weight multimers. N Engl J Med 1982;306:326-333
-
(1982)
N Engl J Med
, vol.306
, pp. 326-333
-
-
Weiss, H.J.1
Meyer, D.2
Rabinowitz, R.3
-
62
-
-
0025896722
-
Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet type von Willebrand's disease
-
Miller CH, Cunningham D, Lyle VA, et al. Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet type von Willebrand's disease. Proc Natl Acad Sci USA 1991;88:4761-4765
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 4761-4765
-
-
Miller, C.H.1
Cunningham, D.2
Lyle, V.A.3
-
63
-
-
0027481159
-
Pseudo-von Willebrand's disease: A mutation in the platelet glycoprotein Ib alpha gene associated with a hyperactive platelet receptor
-
Russell SD, Roth GJ. Pseudo-von Willebrand's disease: a mutation in the platelet glycoprotein Ib alpha gene associated with a hyperactive platelet receptor. Blood 1993;81: 1787-1791
-
(1993)
Blood
, vol.81
, pp. 1787-1791
-
-
Russell, S.D.1
Roth, G.J.2
-
64
-
-
0019303302
-
Identification of membrane proteins mediating the interaction of human platelets
-
Phillips DR, Jennings LK, Edwards HH. Identification of membrane proteins mediating the interaction of human platelets. J Cell Biol 1980;86:77-86
-
(1980)
J Cell Biol
, vol.86
, pp. 77-86
-
-
Phillips, D.R.1
Jennings, L.K.2
Edwards, H.H.3
-
65
-
-
0020692503
-
Studies with a murine monoclonal antibody that abolishes ristocetin induced binding of von Willebrand factor to platelets: Additional evidence in support of GPIb as a platelet receptor for von Willebrand factor
-
Coller BS, Peerschke EI, Scudder LE, et al. Studies with a murine monoclonal antibody that abolishes ristocetin induced binding of von Willebrand factor to platelets: additional evidence in support of GPIb as a platelet receptor for von Willebrand factor. Blood 1983;61:99-110
-
(1983)
Blood
, vol.61
, pp. 99-110
-
-
Coller, B.S.1
Peerschke, E.I.2
Scudder, L.E.3
-
66
-
-
0016862422
-
Specific roles for platelet surface glycoproteins in platelet function
-
Nurden AJ, Caen JP. Specific roles for platelet surface glycoproteins in platelet function. Nature 1975;255:720-722
-
(1975)
Nature
, vol.255
, pp. 720-722
-
-
Nurden, A.J.1
Caen, J.P.2
-
67
-
-
0019973882
-
Characterization of the platelet membrane glycoprotein abnormalities in Bernard Soulier syndrome and comparison with normal with by surface labelling techniques and high resolution two dimensional gel electrophoresis
-
Clementson KJ, McGregor JL, James E, et al. Characterization of the platelet membrane glycoprotein abnormalities in Bernard Soulier syndrome and comparison with normal with by surface labelling techniques and high resolution two dimensional gel electrophoresis. J Clin Invest 1982;70:304-311
-
(1982)
J Clin Invest
, vol.70
, pp. 304-311
-
-
Clementson, K.J.1
McGregor, J.L.2
James, E.3
-
68
-
-
0022649078
-
Von Willebrand factor: A reduced and alkylated 52/48 kDa fragment beginning at amino acid residue 449 contains the domain interacting with platelet glycoprotein Ib
-
Fujimura Y, Titani K, Holland LZ, et al. von Willebrand factor: a reduced and alkylated 52/48 kDa fragment beginning at amino acid residue 449 contains the domain interacting with platelet glycoprotein Ib. J Biol Chem 1986;261:381-385
-
(1986)
J Biol Chem
, vol.261
, pp. 381-385
-
-
Fujimura, Y.1
Titani, K.2
Holland, L.Z.3
-
69
-
-
0013493426
-
Venom coagglutin: An activator of platelet aggregation dependent on von Willebrand factor
-
Read MS, Shermer RW, Brinkhous K. Venom coagglutin: an activator of platelet aggregation dependent on von Willebrand factor. Proc Natl Acad Sci USA 1978;75:4514-4518
-
(1978)
Proc Natl Acad Sci USA
, vol.75
, pp. 4514-4518
-
-
Read, M.S.1
Shermer, R.W.2
Brinkhous, K.3
-
70
-
-
0020427840
-
The agglutination of human platelets by bovine factor VIII
-
Kirby EP. The agglutination of human platelets by bovine factor VIII. J Lab Clin Med 1982;100:963-976
-
(1982)
J Lab Clin Med
, vol.100
, pp. 963-976
-
-
Kirby, E.P.1
-
71
-
-
0022852282
-
Involvement of large plasma von Willebrand factor (VWF) multimers and unusually large VWF forms derived from endothelial cells in shear stress induced platelet aggregation
-
Moake JL, Turner NA, Stathopoulos NA, et al. Involvement of large plasma von Willebrand factor (VWF) multimers and unusually large VWF forms derived from endothelial cells in shear stress induced platelet aggregation. J Clin Invest 1986;78:1456-1461
-
(1986)
J Clin Invest
, vol.78
, pp. 1456-1461
-
-
Moake, J.L.1
Turner, N.A.2
Stathopoulos, N.A.3
-
72
-
-
0025732428
-
The role of von Willebrand factor and fibrinogen in platelet aggregation under shear stress
-
Ikeda Y, Handa M, Kawano K, et al. The role of von Willebrand factor and fibrinogen in platelet aggregation under shear stress. J Clin Invest 1991;87:1234-1240
-
(1991)
J Clin Invest
, vol.87
, pp. 1234-1240
-
-
Ikeda, Y.1
Handa, M.2
Kawano, K.3
-
73
-
-
2342625955
-
Von Willebrand disease: A guideline from the UK Haemophilia Centre Doctors' Organisation
-
Pasi KJ, Collins PW, Keeling DM, et al. von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organisation. Haemophilia 2004;10:218-231
-
(2004)
Haemophilia
, vol.10
, pp. 218-231
-
-
Pasi, K.J.1
Collins, P.W.2
Keeling, D.M.3
-
74
-
-
0030696578
-
Laboratory assays for von Willebrand factor: Relative contribution to the diagnosis of von Willebrand's disease
-
Favaloro EJ, Koutts J. Laboratory assays for von Willebrand factor: relative contribution to the diagnosis of von Willebrand's disease. Pathology 1997;29:385-391
-
(1997)
Pathology
, vol.29
, pp. 385-391
-
-
Favaloro, E.J.1
Koutts, J.2
-
75
-
-
0032860887
-
On behalf of the RCPA quality assurance program (QAP) in haematology-haemostasis scientific advisory panel. Laboratory testing for von Willebrand's disease: An assessment of current diagnostic practice and efficacy by means of a multi-laboratory survey
-
Favaloro EJ, Smith J, Petinos P, et al. On behalf of the RCPA quality assurance program (QAP) in haematology-haemostasis scientific advisory panel. Laboratory testing for von Willebrand's disease: an assessment of current diagnostic practice and efficacy by means of a multi-laboratory survey. Thromb Haemost 1999;82:1276-1282
-
(1999)
Thromb Haemost
, vol.82
, pp. 1276-1282
-
-
Favaloro, E.J.1
Smith, J.2
Petinos, P.3
-
76
-
-
0036240434
-
Laboratory diagnosis of congenital von Willebrand's disease
-
Budde U, Drewke E, Mainusch K, et al. Laboratory diagnosis of congenital von Willebrand's disease. Semin Thromb Hemost 2002;28:173-190
-
(2002)
Semin Thromb Hemost
, vol.28
, pp. 173-190
-
-
Budde, U.1
Drewke, E.2
Mainusch, K.3
-
77
-
-
0036232319
-
A reliable von Willebrand factor: Ristocetin co-factor enzyme linked immunoabsorbent assay to differentiate between type 1 and type 2 von Willebrand's disease
-
Van Hoorelbeke K, Cauwenberghs N, Vandercasteele G, et al. A reliable von Willebrand factor: ristocetin co-factor enzyme linked immunoabsorbent assay to differentiate between type 1 and type 2 von Willebrand's disease. Semin Thromb Hemost 2002;28:161-166
-
(2002)
Semin Thromb Hemost
, vol.28
, pp. 161-166
-
-
Van Hoorelbeke, K.1
Cauwenberghs, N.2
Vandercasteele, G.3
-
78
-
-
0030695365
-
Von Willebrand factor activity detected in a monoclonal antibody based ELISA: An alternative to the ristocetin cofactor platelet agglutination assay for diagnostic use
-
Murdock PJ, Woodhams BJ, Mathews KB, et al. Von Willebrand factor activity detected in a monoclonal antibody based ELISA: an alternative to the ristocetin cofactor platelet agglutination assay for diagnostic use. Thromb Haemost 1997;78:1272-1277
-
(1997)
Thromb Haemost
, vol.78
, pp. 1272-1277
-
-
Murdock, P.J.1
Woodhams, B.J.2
Mathews, K.B.3
-
79
-
-
0026149117
-
Development of a simple collagen based ELISA assay aids in the diagnosis of, and permits sensitive discrimination between type I and type II von Willebrand's disease
-
Favaloro EJ, Grispo L, Exner T, et al. Development of a simple collagen based ELISA assay aids in the diagnosis of, and permits sensitive discrimination between type I and type II von Willebrand's disease. Blood Coagul Fibrinolysis 1991;2:285-291
-
(1991)
Blood Coagul Fibrinolysis
, vol.2
, pp. 285-291
-
-
Favaloro, E.J.1
Grispo, L.2
Exner, T.3
-
80
-
-
0014959015
-
Purification of human anti-haemophilic factor (factor VIII) by gel chromatography
-
van Mourik JA, Mochtar IA. Purification of human anti-haemophilic factor (factor VIII) by gel chromatography. Biochim Biophys Acta 1970;221:677-679
-
(1970)
Biochim Biophys Acta
, vol.221
, pp. 677-679
-
-
Van Mourik, J.A.1
Mochtar, I.A.2
-
81
-
-
0018856312
-
Factor VIII related protein circulates in human plasma as high molecular weight multimers
-
Hoyer IW, Shainoff JR. Factor VIII related protein circulates in human plasma as high molecular weight multimers. Blood 1980;55:1056-1059
-
(1980)
Blood
, vol.55
, pp. 1056-1059
-
-
Hoyer, I.W.1
Shainoff, J.R.2
-
82
-
-
0018123566
-
Disulfide bonds and the quaternary structure of factor VIII/von Willebrand factor
-
Counts RB, Paskell SL, Elgee S. Disulfide bonds and the quaternary structure of factor VIII/von Willebrand factor. J Clin Invest 1978;62:702-709
-
(1978)
J Clin Invest
, vol.62
, pp. 702-709
-
-
Counts, R.B.1
Paskell, S.L.2
Elgee, S.3
-
83
-
-
0017862590
-
Heterogeneity of human Factor VIII. I. Characterisation of factor VIII present in the supernatant of cryoprecipitate
-
Over J, Bouma BM, van Mourik JA, et al. Heterogeneity of human Factor VIII. I. Characterisation of factor VIII present in the supernatant of cryoprecipitate. J Lab Clin Med 1978;91:32-46
-
(1978)
J Lab Clin Med
, vol.91
, pp. 32-46
-
-
Over, J.1
Bouma, B.M.2
Van Mourik, J.A.3
-
84
-
-
0017816125
-
Predominance of normal low molecular weight forms of factor VIII in "variant" von Willebrand's disease
-
Sixma JJ, Over J, Bouma BN, et al. Predominance of normal low molecular weight forms of factor VIII in "variant" von Willebrand's disease. Thromb Res 1978;12:929-935
-
(1978)
Thromb Res
, vol.12
, pp. 929-935
-
-
Sixma, J.J.1
Over, J.2
Bouma, B.N.3
-
85
-
-
0019496229
-
Effect of multimeric structure of factor VIII/von Willebrand factor protein on binding to platelets
-
Gralnick HR, Williams SB, Morisato DK. Effect of multimeric structure of factor VIII/von Willebrand factor protein on binding to platelets. Blood 1981;58:387-397
-
(1981)
Blood
, vol.58
, pp. 387-397
-
-
Gralnick, H.R.1
Williams, S.B.2
Morisato, D.K.3
-
86
-
-
0016293718
-
Variant pattern of von Willebrand's disease
-
Koutts J, Stott L, Sawers RJ. Variant pattern of von Willebrand's disease. Thomb Research 1974;5:557-564
-
(1974)
Thomb Research
, vol.5
, pp. 557-564
-
-
Koutts, J.1
Stott, L.2
Sawers, R.J.3
-
87
-
-
0023612519
-
Von Willebrand factor and von Willebrand disease
-
Ruggeri ZM, Zimmerman TS. Von Willebrand factor and von Willebrand disease. Blood 1987;70:895-904
-
(1987)
Blood
, vol.70
, pp. 895-904
-
-
Ruggeri, Z.M.1
Zimmerman, T.S.2
-
88
-
-
0015495140
-
Genetic variants of von Willebrand's disease
-
Holmberg L, Nilsson IM. Genetic variants of von Willebrand's disease. BMJ 1972;3:317-320
-
(1972)
BMJ
, vol.3
, pp. 317-320
-
-
Holmberg, L.1
Nilsson, I.M.2
-
89
-
-
0015811736
-
Von Willebrand's disease type B: A newly defined bleeding diathesis
-
Firkin B, Firkin F, Stott L. von Willebrand's disease type B: a newly defined bleeding diathesis. Aust NZ J Med 1973; 3:225-229
-
(1973)
Aust NZ J Med
, vol.3
, pp. 225-229
-
-
Firkin, B.1
Firkin, F.2
Stott, L.3
-
90
-
-
0016348528
-
Willebrand factor and ristocetin. II. Relationship between Willebrand factor, Willebrand antigen and factor VIII activity
-
Meyer D, Jenkins CSP, Dreyfus MD, et al. Willebrand factor and ristocetin. II. Relationship between Willebrand factor, Willebrand antigen and factor VIII activity. Br J Haematol 1974;28:579-599
-
(1974)
Br J Haematol
, vol.28
, pp. 579-599
-
-
Meyer, D.1
Jenkins, C.S.P.2
Dreyfus, M.D.3
-
91
-
-
0016147023
-
Inherited variants of factor VIII related protein in von Willebrand's disease
-
Peake IR, Bloom AL, Giddings JC. Inherited variants of factor VIII related protein in von Willebrand's disease. N Engl J Med 1974;291:113-117
-
(1974)
N Engl J Med
, vol.291
, pp. 113-117
-
-
Peake, I.R.1
Bloom, A.L.2
Giddings, J.C.3
-
92
-
-
0025008771
-
Severe type III von Willebrand's disease caused by deletions of exon42 of the von Willebrand factor gene: Family studies that identify carriers of the condition and compound heterozygous individuals
-
Peake IR, Liddel MB, Moodie P, et al. Severe type III von Willebrand's disease caused by deletions of exon42 of the von Willebrand factor gene: family studies that identify carriers of the condition and compound heterozygous individuals. Blood 1990;75:654-661
-
(1990)
Blood
, vol.75
, pp. 654-661
-
-
Peake, I.R.1
Liddel, M.B.2
Moodie, P.3
-
93
-
-
0028027430
-
Genetic heterogeneity of severe von Willebrand disease type III in the German population
-
Schneppenheim R, Kreey 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
Kreey, S.2
Bergmann, F.3
-
94
-
-
0026640029
-
Nonsense mutations of the von Willebrand gene in patients with von Willebrand disease type III and type I
-
Zhang ZP, Lindsedt M, Falk G, et al. Nonsense mutations of the von Willebrand 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
Lindsedt, M.2
Falk, G.3
-
95
-
-
0017143871
-
Precipitating antibodies in von Willebrand's disease
-
Mannucci PM, Meyer D, Ruggeri ZM, et al. Precipitating antibodies in von Willebrand's disease. Nature 1976;262: 141-142
-
(1976)
Nature
, vol.262
, pp. 141-142
-
-
Mannucci, P.M.1
Meyer, D.2
Ruggeri, Z.M.3
-
96
-
-
0028285840
-
Commentary: A new classification for von Willebrand's disease
-
Sadler JE, Gralnick HR. Commentary: a new classification for von Willebrand's disease. Blood 1994;84:676-679
-
(1994)
Blood
, vol.84
, pp. 676-679
-
-
Sadler, J.E.1
Gralnick, H.R.2
-
97
-
-
0020464357
-
Variant von Willebrand's disease type B revisited
-
Howard MA, Salem HH, Thomas KB, et al. Variant von Willebrand's disease type B revisited. Blood 1982;60:1420-1428
-
(1982)
Blood
, vol.60
, pp. 1420-1428
-
-
Howard, M.A.1
Salem, H.H.2
Thomas, K.B.3
-
98
-
-
0023852791
-
Von Willebrand disease "Vicenza" with larger than normal (supra-normal) von Willebrand factor multimers
-
Mannucci PM, Lombardi R, Castaman C, et al. Von Willebrand disease "Vicenza" with larger than normal (supra-normal) von Willebrand factor multimers. Blood 1988;71:65-70
-
(1988)
Blood
, vol.71
, pp. 65-70
-
-
Mannucci, P.M.1
Lombardi, R.2
Castaman, C.3
-
99
-
-
0022405292
-
High resolution analysis of von Willebrand factor multimeric composition defines a new variant of type 1 von Willebrand's disease with aberrant structure, but presence of all size multimers (type 1C)
-
Ciavarella G, Ciavarella N, Antoncecchi S, et al. High resolution analysis of von Willebrand factor multimeric composition defines a new variant of type 1 von Willebrand's disease with aberrant structure, but presence of all size multimers (type 1C). Blood 1985;66:1423-1429
-
(1985)
Blood
, vol.66
, pp. 1423-1429
-
-
Ciavarella, G.1
Ciavarella, N.2
Antoncecchi, S.3
-
100
-
-
0026630044
-
Impaired intracellular transport produced by a subset of Type IIA von Willebrand disease mutations
-
Lyons SE, Bruck ME, Bowie EJ, et al. Impaired intracellular transport produced by a subset of Type IIA von Willebrand disease mutations. J Biol Chem 1992;267:4424-4430
-
(1992)
J Biol Chem
, vol.267
, pp. 4424-4430
-
-
Lyons, S.E.1
Bruck, M.E.2
Bowie, E.J.3
-
101
-
-
0025044664
-
Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in Type IIA von Willebrand factor
-
Dent JA, Berkowitz SD, Ware J, et al. Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in Type IIA von Willebrand factor. Proc Natl Acad Sci USA 1990;87:6306-6310
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 6306-6310
-
-
Dent, J.A.1
Berkowitz, S.D.2
Ware, J.3
-
102
-
-
0029916821
-
Defective dimerization of von Willebrand factor subunits due to a Cys-Arg mutation in Type HD von Willebrand disease
-
Schneppenheim R, Brassard J, Kray S, et al. Defective dimerization of von Willebrand factor subunits due to a Cys-Arg mutation in Type HD von Willebrand disease. Proc Natl Acad Sci USA 1996;93:3581-3586
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 3581-3586
-
-
Schneppenheim, R.1
Brassard, J.2
Kray, S.3
-
103
-
-
33746588145
-
-
Hoffmann R, Benz EJ, Shattil SJ, et al, eds. Philadelphia, PA: Churchill Livingstone
-
Ginsburg D, Wagner DD. In: Hoffmann R, Benz EJ, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 4th ed. Philadelphia, PA: Churchill Livingstone; 2005:2111-2114
-
(2005)
Hematology: Basic Principles and Practice. 4th Ed.
, pp. 2111-2114
-
-
Ginsburg, D.1
Wagner, D.D.2
-
104
-
-
0014712629
-
Molecular forms of antihemophilic globulins in plasma, cryoprecipitate and after thrombin activation
-
Weiss HJ, Kochwa S. Molecular forms of antihemophilic globulins in plasma, cryoprecipitate and after thrombin activation. Br J Haematol 1970;18:89-100
-
(1970)
Br J Haematol
, vol.18
, pp. 89-100
-
-
Weiss, H.J.1
Kochwa, S.2
-
105
-
-
0015923364
-
Von Willebrand factor: Dissociation from antihemophilic factor procoagulant activity
-
Weiss HJ, Hoyer LW. Von Willebrand factor: dissociation from antihemophilic factor procoagulant activity. Science 1973;182:1149-1151
-
(1973)
Science
, vol.182
, pp. 1149-1151
-
-
Weiss, H.J.1
Hoyer, L.W.2
-
106
-
-
0015530864
-
Antihemophilic factor separation of an active fragment following dissociation by salts and detergents
-
Owen WG, Wagner RH. Antihemophilic factor separation of an active fragment following dissociation by salts and detergents. Thromb Diath Haemorrh 1972;27:502-515
-
(1972)
Thromb Diath Haemorrh
, vol.27
, pp. 502-515
-
-
Owen, W.G.1
Wagner, R.H.2
-
107
-
-
0015819659
-
Factor VIII coagulant activity and factor VIII like antigen: Independent molecular entities
-
Zimmerman TS, Edgington TS. Factor VIII coagulant activity and factor VIII like antigen: independent molecular entities. J Exp Med 1973;138:1015-1020
-
(1973)
J Exp Med
, vol.138
, pp. 1015-1020
-
-
Zimmerman, T.S.1
Edgington, T.S.2
-
108
-
-
0017136222
-
The dynamic interrelationship between factor VIII and von Willebrand factor
-
Koutts J, Gude N, Firkin BG. The dynamic interrelationship between factor VIII and von Willebrand factor. Thromb Res 1976;8:533-541
-
(1976)
Thromb Res
, vol.8
, pp. 533-541
-
-
Koutts, J.1
Gude, N.2
Firkin, B.G.3
-
109
-
-
0017587026
-
Immunological evidence that human factor VIII is composed of two moieties
-
Koutts J, Lavergne JM, Meyer D. Immunological evidence that human factor VIII is composed of two moieties. Br J Haematol 1977;37:415-427
-
(1977)
Br J Haematol
, vol.37
, pp. 415-427
-
-
Koutts, J.1
Lavergne, J.M.2
Meyer, D.3
-
110
-
-
0023217139
-
A major factor VIII binding domain resides within the amino terminal 272 amino acid residues of von Willebrand factor
-
Foster PA, Fulcher CA, Marti T, et al. A major factor VIII binding domain resides within the amino terminal 272 amino acid residues of von Willebrand factor. J Biol Chem 1987;262:8443-8446
-
(1987)
J Biol Chem
, vol.262
, pp. 8443-8446
-
-
Foster, P.A.1
Fulcher, C.A.2
Marti, T.3
-
111
-
-
0017754787
-
Stabilization of factor VIII in plasma by the von Willebrand factor
-
Weiss HJ, Sussman II, Hoyer LW. Stabilization of factor VIII in plasma by the von Willebrand factor. J Clin Invest 1977;60:390-404
-
(1977)
J Clin Invest
, vol.60
, pp. 390-404
-
-
Weiss, H.J.1
Sussman, I.I.2
Hoyer, L.W.3
-
112
-
-
0024425034
-
New variant of von Willebrand's disease with defective binding to factor VIII
-
Nishino M, Girma J-P, Rothschild C, et al. New variant of von Willebrand's disease with defective binding to factor VIII. Blood 1989;74:1591-1599
-
(1989)
Blood
, vol.74
, pp. 1591-1599
-
-
Nishino, M.1
Girma, J.-P.2
Rothschild, C.3
-
113
-
-
0037443406
-
Von Willebrand disease type: A diagnosis in search of a disease
-
Sadler JE. Von Willebrand disease type: a diagnosis in search of a disease. Blood 2003;101:2089-2093
-
(2003)
Blood
, vol.101
, pp. 2089-2093
-
-
Sadler, J.E.1
-
114
-
-
0036588833
-
Willebrand disease: Still an intriguing disorder in the era of molecular medicine
-
Rodeghiero F. Willebrand disease: still an intriguing disorder in the era of molecular medicine. Haemophilia 2002; 8:292-300
-
(2002)
Haemophilia
, vol.8
, pp. 292-300
-
-
Rodeghiero, F.1
-
115
-
-
0019968574
-
Estrogen and surgery in women with von Willebrand's disease
-
Alperin JB. Estrogen and surgery in women with von Willebrand's disease. Am J Med 1982;73:367-371
-
(1982)
Am J Med
, vol.73
, pp. 367-371
-
-
Alperin, J.B.1
-
116
-
-
0019411310
-
The factor VIII complex: Structure and function
-
Hoyer LW. The factor VIII complex: structure and function. Blood 1981;58:1-13
-
(1981)
Blood
, vol.58
, pp. 1-13
-
-
Hoyer, L.W.1
-
117
-
-
0023257218
-
The effect of ABO blood group on the diagnosis of von Willebrand disease
-
Gill JC, Endres-Brooks J, Bauer PJ, et al. The effect of ABO blood group on the diagnosis of von Willebrand disease. Blood 1987;69:1691-1695
-
(1987)
Blood
, vol.69
, pp. 1691-1695
-
-
Gill, J.C.1
Endres-Brooks, J.2
Bauer, P.J.3
-
118
-
-
0024421194
-
Heterogeneous phenotypes of platelet and plasma von Willebrand factor in obligatory heterozygotes for severe von Willebrand disease
-
Mannucci PM, Lattuada A, Castaman G, et al. Heterogeneous phenotypes of platelet and plasma von Willebrand factor in obligatory heterozygotes for severe von Willebrand disease. Blood 1989;74:2433-2436
-
(1989)
Blood
, vol.74
, pp. 2433-2436
-
-
Mannucci, P.M.1
Lattuada, A.2
Castaman, G.3
-
119
-
-
0031239285
-
Von Willebrand disease and quantitative variation in von Willebrand factor
-
Mohlke KL, Ginsbrg D. Von Willebrand disease and quantitative variation in von Willebrand factor. J Lab Clin Med 1997;130:252-261
-
(1997)
J Lab Clin Med
, vol.130
, pp. 252-261
-
-
Mohlke, K.L.1
Ginsbrg, D.2
-
120
-
-
0027458101
-
Prevalence of von Willebrand disease in children: A multicentre study
-
Werner EJ, Broxson EH, Tucker EL, et al. Prevalence of von Willebrand disease in children: a multicentre 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
-
121
-
-
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
-
122
-
-
0032823229
-
Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation
-
Castaman G, Eikenboom JCL, Bertina RM, et al. Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation. Thromb Haemost 1999;82: 1065-1070
-
(1999)
Thromb Haemost
, vol.82
, pp. 1065-1070
-
-
Castaman, G.1
Eikenboom, J.C.L.2
Bertina, R.M.3
-
123
-
-
0033858187
-
Impact, diagnosis and treatment of von Willebrand disease
-
Sadler JE, Mannucci PM, Berntrop E, et al. Impact, diagnosis and treatment of von Willebrand disease. Thromb Haemost 2000;84:160-174
-
(2000)
Thromb Haemost
, vol.84
, pp. 160-174
-
-
Sadler, J.E.1
Mannucci, P.M.2
Berntrop, E.3
-
124
-
-
0031825529
-
Females with von Willebrand's disease: 72 years as the silent majority
-
Kouides PA. Females with von Willebrand's disease: 72 years as the silent majority. Haemophilia 1998;4:665-676
-
(1998)
Haemophilia
, vol.4
, pp. 665-676
-
-
Kouides, P.A.1
-
125
-
-
0036588676
-
Menorrhagia from a haematologist's point of view. Part 1: Initial evaluation
-
Kouides PA. Menorrhagia from a haematologist's point of view. Part 1: initial evaluation. Haemophilia 2002;8:330-338
-
(2002)
Haemophilia
, vol.8
, pp. 330-338
-
-
Kouides, P.A.1
-
126
-
-
0029038085
-
The reproductive health of women with von Willebrand disease unresponsive to DDAVP-results of an international survey
-
Foster PA. The reproductive health of women with von Willebrand disease unresponsive to DDAVP-results of an international survey. Thromb Haemost 1995;74:784-790
-
(1995)
Thromb Haemost
, vol.74
, pp. 784-790
-
-
Foster, P.A.1
-
127
-
-
0033486280
-
Preoperative screening for von Willebrand disease type 1: Low yield and limited ability to predict bleeding
-
Biron C, Mahieu B, Rochette P, et al. Preoperative screening for von Willebrand disease type 1: low yield and limited ability to predict bleeding. J Lab Clin Med 1999; 134:605-609
-
(1999)
J Lab Clin Med
, vol.134
, pp. 605-609
-
-
Biron, C.1
Mahieu, B.2
Rochette, P.3
-
128
-
-
33746628874
-
-
Hoffman R, Benz EJ, Shattil SJ, et al, eds. Philadelphia, PA: Churchill Livingstone
-
Coller BS, Schneiderham PI. In: Hoffman R, Benz EJ, Shattil SJ, et al, eds. Haematology: Basic Principles and Practice. 4th ed. Philadelphia, PA: Churchill Livingstone; 2005:1976-1982
-
(2005)
Haematology: Basic Principles and Practice. 4th Ed.
, pp. 1976-1982
-
-
Coller, B.S.1
Schneiderham, P.I.2
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