-
1
-
-
77049208954
-
A familial hemorrhagic trait associated with a deficiency of a clot-promoting fraction of plasma
-
Ratnoff OD, Colepy JE. A familial hemorrhagic trait associated with a deficiency of a clot-promoting fraction of plasma. J Clin Invest 1955;34:602.
-
(1955)
J Clin Invest
, vol.34
, pp. 602
-
-
Ratnoff, O.D.1
Colepy, J.E.2
-
2
-
-
0003072114
-
Contact activation pathway: Inflammatory, fibrinolytic, anticoagulant, antiadhesive and antiangiogenic activities
-
Colmar RW, Hirsh J, Marder VJ, Clowes AW, Teorge JM, eds. Philadelphia: Lippincott, Williams, and Wilkins
-
Colman RW. Contact activation pathway: Inflammatory, fibrinolytic, anticoagulant, antiadhesive and antiangiogenic activities. In: Colmar RW, Hirsh J, Marder VJ, Clowes AW, Teorge JM, eds. Thrombosis and Haemostasis, 4th ed. Philadelphia: Lippincott, Williams, and Wilkins, 2001.
-
(2001)
Thrombosis and Haemostasis, 4th Ed.
-
-
Colman, R.W.1
-
3
-
-
0021799672
-
Rarer quantitative and qualitative abnormalities of coagulation
-
Girolami A, De Marco L, Dal Bo Zanon R, Patrassi G, Cappellato MG. Rarer quantitative and qualitative abnormalities of coagulation. Clin Haematol 1985;14:385.
-
(1985)
Clin Haematol
, vol.14
, pp. 385
-
-
Girolami, A.1
De Marco, L.2
Dal Bo Zanon, R.3
Patrassi, G.4
Cappellato, M.G.5
-
4
-
-
0342443183
-
Hageman factor deficiency (Hageman Trait)
-
Didisheim P. Hageman factor deficiency (Hageman Trait). Arch Intern Med 1962;110:170.
-
(1962)
Arch Intern Med
, vol.110
, pp. 170
-
-
Didisheim, P.1
-
6
-
-
0027351136
-
Factor FXII (Hageman factor) deficiency: A risk factor for development of thromboembolism. Incidence of factor XII deficiency in patients after recurrent venous or arterial thromboemboplism and myocardial infarction
-
Halbmayer WM, Mannhalter C, Feichtinger C, Rubi K, Fischer M. Factor FXII (Hageman factor) deficiency: A risk factor for development of thromboembolism. Incidence of factor XII deficiency in patients after recurrent venous or arterial thromboemboplism and myocardial infarction. Wien Med Wochenschr 1993;143:43.
-
(1993)
Wien Med Wochenschr
, vol.143
, pp. 43
-
-
Halbmayer, W.M.1
Mannhalter, C.2
Feichtinger, C.3
Rubi, K.4
Fischer, M.5
-
7
-
-
0020693702
-
Arterial and venous thrombosis and normal response to streptokinase treatment in a young patient with severe Hageman factor deficiency
-
Hellstern P, Kohler M, Schmengler K, Doenecke P, Wenzel E. Arterial and venous thrombosis and normal response to streptokinase treatment in a young patient with severe Hageman factor deficiency. Acta Haematol 1983;69:123.
-
(1983)
Acta Haematol
, vol.69
, pp. 123
-
-
Hellstern, P.1
Kohler, M.2
Schmengler, K.3
Doenecke, P.4
Wenzel, E.5
-
8
-
-
0003371207
-
Factor XII activity and antigen concentrations in patients suffering from recurrant thrombosis
-
Mannhalter C, Fischer M, Hopmaier P, Deutch E. Factor XII activity and antigen concentrations in patients suffering from recurrant thrombosis. Fibrinolysis 1987;1:259.
-
(1987)
Fibrinolysis
, vol.1
, pp. 259
-
-
Mannhalter, C.1
Fischer, M.2
Hopmaier, P.3
Deutch, E.4
-
9
-
-
0026065260
-
Thromboembolism and bleeding tendency in congenital factor XII deficiency. A study on 74 subjects from 14 Swiss families
-
Lämmle B, Wuillemin WA, Huber I, et al. Thromboembolism and bleeding tendency in congenital factor XII deficiency. A study on 74 subjects from 14 Swiss families. Thromb Haemost 1991;65:117.
-
(1991)
Thromb Haemost
, vol.65
, pp. 117
-
-
Lämmle, B.1
Wuillemin, W.A.2
Huber, I.3
-
10
-
-
0020565895
-
Thrombosis or myocardial infartction in congenital clotting factor abnormalities and chronic thrombocytopenias: A report of 21 patients and a review of 50 previously reported cases
-
Goodnough LT, Saito H, Ratnoff OD. Thrombosis or myocardial infartction in congenital clotting factor abnormalities and chronic thrombocytopenias: A report of 21 patients and a review of 50 previously reported cases. Medicine 1983;62:248.
-
(1983)
Medicine
, vol.62
, pp. 248
-
-
Goodnough, L.T.1
Saito, H.2
Ratnoff, O.D.3
-
14
-
-
6344220423
-
Hageman trait (Hageman factor deficiency)
-
Jim RT, Goldfein S. Hageman trait (Hageman factor deficiency). Am J Med 1957;23:824.
-
(1957)
Am J Med
, vol.23
, pp. 824
-
-
Jim, R.T.1
Goldfein, S.2
-
15
-
-
1542790984
-
Repair of cardiac defect in patient with Ehlers-Danlos syndrome and deficiency of Hageman Factor
-
Fantl P, Morris KN, Savers RJ. Repair of cardiac defect in patient with Ehlers-Danlos syndrome and deficiency of Hageman Factor. BMJ 1961:1202.
-
(1961)
BMJ
, pp. 1202
-
-
Fantl, P.1
Morris, K.N.2
Savers, R.J.3
-
16
-
-
0014233442
-
Hageman factor deficiency
-
Miwa S, Asai I, Tsukada T, Shimizu M, Teramura K, Sunaga Y. Hageman factor deficiency. Acta Haemat 1968;39:36.
-
(1968)
Acta Haemat
, vol.39
, pp. 36
-
-
Miwa, S.1
Asai, I.2
Tsukada, T.3
Shimizu, M.4
Teramura, K.5
Sunaga, Y.6
-
17
-
-
0023625055
-
Major Abdominal surgery on a patient with factor XII deficiency and lupus anticoagulant: Postoperative DUT as judged by the fibrinogen uptake test
-
Nilsson TK, Mallbring G. Major Abdominal surgery on a patient with factor XII deficiency and lupus anticoagulant: Postoperative DUT as judged by the fibrinogen uptake test. Clin Thromb Haemost 1982;9:415.
-
(1982)
Clin Thromb Haemost
, vol.9
, pp. 415
-
-
Nilsson, T.K.1
Mallbring, G.2
-
18
-
-
0022296657
-
Congenital factor XII deficiency: Successful open heart surgery and anticoagulation
-
Kelsey PR, Films JB, Grette GJ, Maciver JE. Congenital factor XII deficiency: Successful open heart surgery and anticoagulation. Thromb Haemost 1985;7:379.
-
(1985)
Thromb Haemost
, vol.7
, pp. 379
-
-
Kelsey, P.R.1
Films, J.B.2
Grette, G.J.3
Maciver, J.E.4
-
20
-
-
0018762751
-
Effect of FXII deficiency on pregnancy and parturition
-
Saidi P, Siegelman M, Mitchel VB. Effect of FXII deficiency on pregnancy and parturition. Thromb Haemost 1979;41:523.
-
(1979)
Thromb Haemost
, vol.41
, pp. 523
-
-
Saidi, P.1
Siegelman, M.2
Mitchel, V.B.3
-
21
-
-
0014353441
-
Congenital deficiency of Hageman factor (clotting factor XII)
-
Benamou B, Streub PW. Congenital deficiency of Hageman factor (clotting factor XII). Helv Med Acta 1968;34:313.
-
(1968)
Helv Med Acta
, vol.34
, pp. 313
-
-
Benamou, B.1
Streub, P.W.2
-
22
-
-
0014834193
-
A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): Study of a large kindren
-
Girolami A, Molaro G, Lazzarin M, Scarpa R, Brunetti A. A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): Study of a large kindren. Br J Haematol 1970;19:179.
-
(1970)
Br J Haematol
, vol.19
, pp. 179
-
-
Girolami, A.1
Molaro, G.2
Lazzarin, M.3
Scarpa, R.4
Brunetti, A.5
-
23
-
-
0342710883
-
Lack of factor XII antigen in factor XII deficiency as determined by electroimmunoassay
-
Girolami A, Patrassi G, De Marco L, Cappellato G. Lack of factor XII antigen in factor XII deficiency as determined by electroimmunoassay. Blut 1982;45:141.
-
(1982)
Blut
, vol.45
, pp. 141
-
-
Girolami, A.1
Patrassi, G.2
De Marco, L.3
Cappellato, G.4
-
24
-
-
0034030849
-
Symptomatic combined homozygous factor XII deficiency and heterozygous factor V Leiden
-
Girolami A, Simioni P, Scarano L, Girolami B, Zerbinati P. Symptomatic combined homozygous factor XII deficiency and heterozygous factor V Leiden. J Thromb Thrombolysis 2000;9:271.
-
(2000)
J Thromb Thrombolysis
, vol.9
, pp. 271
-
-
Girolami, A.1
Simioni, P.2
Scarano, L.3
Girolami, B.4
Zerbinati, P.5
-
25
-
-
0027015750
-
Functional anomaly of factor XII
-
Aznar J, Villa P, Vega A, Mira Y, Lorenzo I, Esperia F. Functional anomaly of factor XII. Hemostasis 1992;22: 345.
-
(1992)
Hemostasis
, vol.22
, pp. 345
-
-
Aznar, J.1
Villa, P.2
Vega, A.3
Mira, Y.4
Lorenzo, I.5
Esperia, F.6
-
26
-
-
0018829404
-
A quarter century with Mr. Hageman
-
Ratnoff OD. A quarter century with Mr. Hageman. Thromb Haemost 1980;43:95.
-
(1980)
Thromb Haemost
, vol.43
, pp. 95
-
-
Ratnoff, O.D.1
-
28
-
-
0032825571
-
Revaluation of the incidence of thromboembolic complication in congenital factor XII deficiency. A study on 73 subject from 14 Swiss families
-
Zeerleder S, Schloenner M, Redondo M, et al. Revaluation of the incidence of thromboembolic complication in congenital factor XII deficiency. A study on 73 subject from 14 Swiss families. Thromb Haemost 1999;82:1240.
-
(1999)
Thromb Haemost
, vol.82
, pp. 1240
-
-
Zeerleder, S.1
Schloenner, M.2
Redondo, M.3
-
31
-
-
0024294854
-
Variation of factor XII level during pregnancy in a woman with Hageman factor deficiency
-
Schved JF, Grisb JL, Neven S, Mares P, Sarlat C. Variation of factor XII level during pregnancy in a woman with Hageman factor deficiency. Thromb Haemost 1988;60: 526.
-
(1988)
Thromb Haemost
, vol.60
, pp. 526
-
-
Schved, J.F.1
Grisb, J.L.2
Neven, S.3
Mares, P.4
Sarlat, C.5
-
32
-
-
4344705675
-
Should factor XII assays be included in thombophilia screening?
-
Winter M, Gallimore M, Jones DW. Should factor XII assays be included in thombophilia screening? Lancet 1995;346:352.
-
(1995)
Lancet
, vol.346
, pp. 352
-
-
Winter, M.1
Gallimore, M.2
Jones, D.W.3
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