-
1
-
-
85025505681
-
Hemostasis: General considerations
-
Miller DR, Baehner RL, editors. St. Louis: CV Mosby
-
Corrigan J. Hemostasis: general considerations. In: Miller DR, Baehner RL, editors. Blood diseases of infancy and childhood. St. Louis: CV Mosby, 1990: 761-76
-
(1990)
Blood Diseases of Infancy and Childhood
, pp. 761-776
-
-
Corrigan, J.1
-
2
-
-
0026766155
-
The structure and function of von Willebrand factor
-
Ruggeri ZM, Ware J. The structure and function of von Willebrand factor. Thromb Haemost 1992; 67: 594-9
-
(1992)
Thromb Haemost
, vol.67
, pp. 594-599
-
-
Ruggeri, Z.M.1
Ware, J.2
-
3
-
-
13344276582
-
Requirements of von Willebrand factor to protect factor VIII from inactivation by activated protein C
-
Koppelman SJ, van Hoeij M, Vink T, Lankhof H, Schiphorst ME, Damas C, et al. Requirements of von Willebrand factor to protect factor VIII from inactivation by activated protein C. Blood 1996; 87: 2292-300
-
(1996)
Blood
, vol.87
, pp. 2292-2300
-
-
Koppelman, S.J.1
Van Hoeij, M.2
Vink, T.3
Lankhof, H.4
Schiphorst, M.E.5
Damas, C.6
-
4
-
-
0028201807
-
A revised classification of von Willebrand disease
-
Sadler JE. A revised classification of von Willebrand disease. Thromb Haemost 1994; 71: 520-5
-
(1994)
Thromb Haemost
, vol.71
, pp. 520-525
-
-
Sadler, J.E.1
-
6
-
-
0026803207
-
The prevalence of factor XII deficiency in 103 orally anticoagulated outpatients suffering from recurrent venous and/ or arterial thromboembolism
-
Halbmayer WM, Mannhalter C, Feichtinger C, Rubi K, Fischer M. The prevalence of factor XII deficiency in 103 orally anticoagulated outpatients suffering from recurrent venous and/ or arterial thromboembolism. Thromb Haemost 1992; 68: 285-90
-
(1992)
Thromb Haemost
, vol.68
, pp. 285-290
-
-
Halbmayer, W.M.1
Mannhalter, C.2
Feichtinger, C.3
Rubi, K.4
Fischer, M.5
-
7
-
-
0018829404
-
A quarter century with Mr. Hageman
-
Ratnoff OD. A quarter century with Mr. Hageman. Thromb Haemost 1980; 43: 95-8
-
(1980)
Thromb Haemost
, vol.43
, pp. 95-98
-
-
Ratnoff, O.D.1
-
8
-
-
0025867114
-
Decreased factor XII activity in a child with nephrotic syndrome and thromboembolic complications
-
Négrier C, Delmas MC, Ranchin B, Cochat P, Dechavanne M. Decreased factor XII activity in a child with nephrotic syndrome and thromboembolic complications. Thromb Haemost 1991; 66: 512-3
-
(1991)
Thromb Haemost
, vol.66
, pp. 512-513
-
-
Négrier, C.1
Delmas, M.C.2
Ranchin, B.3
Cochat, P.4
Dechavanne, M.5
-
9
-
-
0028244236
-
Antiphospholipid and thrombosis syndrome
-
Bick RL, Baker WF. Antiphospholipid and thrombosis syndrome. Semin Thromb Hemost 1994; 20: 3-15
-
(1994)
Semin Thromb Hemost
, vol.20
, pp. 3-15
-
-
Bick, R.L.1
Baker, W.F.2
-
10
-
-
0023686724
-
A frequent factor XII gene mutation in Hageman trait
-
Bernardi F, Marchetti G, Volinia S, Patracchini P, Casonato A, Girolami A, et al. A frequent factor XII gene mutation in Hageman trait. Hum Genet 1988; 80: 149-51
-
(1988)
Hum Genet
, vol.80
, pp. 149-151
-
-
Bernardi, F.1
Marchetti, G.2
Volinia, S.3
Patracchini, P.4
Casonato, A.5
Girolami, A.6
-
11
-
-
0028584461
-
Childhood stroke at three years of age with transient protein C deficiency, familial antiphospholipid antibodies and F XII deficiency - A family study
-
Korte W, Otremba H, Lutz S, Flury R, Schmidt L, Weissert M. Childhood stroke at three years of age with transient protein C deficiency, familial antiphospholipid antibodies and F XII deficiency - a family study. Neuropediatrics 1994; 25: 290-4
-
(1994)
Neuropediatrics
, vol.25
, pp. 290-294
-
-
Korte, W.1
Otremba, H.2
Lutz, S.3
Flury, R.4
Schmidt, L.5
Weissert, M.6
-
12
-
-
0017113771
-
Von Willebrand disease San Diego, a new variant
-
Cramer AD, Melaragno AJ, Phifer SJ, Hougie C. Von Willebrand disease San Diego, a new variant. Lancet 1976; 2: 12-4
-
(1976)
Lancet
, vol.2
, pp. 12-14
-
-
Cramer, A.D.1
Melaragno, A.J.2
Phifer, S.J.3
Hougie, C.4
-
13
-
-
0020042441
-
Additional factor XII (Hageman factor) deficiency in hemophilia A and in von Willebrand syndrome
-
Barthels M, Edel J, Liese B, Karge HE. Additional factor XII (Hageman factor) deficiency in hemophilia A and in von Willebrand syndrome. Klin Wochenschr 1982; 60: 303-9
-
(1982)
Klin Wochenschr
, vol.60
, pp. 303-309
-
-
Barthels, M.1
Edel, J.2
Liese, B.3
Karge, H.E.4
-
14
-
-
0026045280
-
Laboratory diagnosis of von Willebrand's disease
-
Triplett D. Laboratory diagnosis of von Willebrand's disease. Mayo Clin Proc 1991; 66: 832-40
-
(1991)
Mayo Clin Proc
, vol.66
, pp. 832-840
-
-
Triplett, D.1
-
15
-
-
0023787137
-
Development of the human coagulation system in the healthy premature infant
-
Andrew M, Paes B, Milner R, Johnston M, Mitchell L, Tollefsen DM, et al. Development of the human coagulation system in the healthy premature infant. Blood 1988; 72: 1651-7
-
(1988)
Blood
, vol.72
, pp. 1651-1657
-
-
Andrew, M.1
Paes, B.2
Milner, R.3
Johnston, M.4
Mitchell, L.5
Tollefsen, D.M.6
-
16
-
-
0027524482
-
Structural biology, cellular interactions and pathophysiology of the contact system
-
Wachtfogel Y, DeLa Cadena R, Culman R. Structural biology, cellular interactions and pathophysiology of the contact system. Thromb Res 1993, 72: 1-21
-
(1993)
Thromb Res
, vol.72
, pp. 1-21
-
-
Wachtfogel, Y.1
Dela Cadena, R.2
Culman, R.3
|