-
1
-
-
4043144279
-
Haemophilia and thrombophilia: an unexpected association!
-
Dargaud Y, Meunier S, Negrier C. Haemophilia and thrombophilia: an unexpected association! Haemophilia 2004; 10: 319-26.
-
(2004)
Haemophilia
, vol.10
, pp. 319-326
-
-
Dargaud, Y.1
Meunier, S.2
Negrier, C.3
-
2
-
-
24944508772
-
Myocardial infarction, other arterial thrombosis and invasive coronary procedures, in hemaophilia B: a critical evaluation of reported cases
-
Girolami A, Randi ML, Ruzzon E, Zanon E, Girolami B. Myocardial infarction, other arterial thrombosis and invasive coronary procedures, in hemaophilia B: a critical evaluation of reported cases. J Thromb Thromboly 2005; 20: 43-6.
-
(2005)
J Thromb Thromboly
, vol.20
, pp. 43-46
-
-
Girolami, A.1
Randi, M.L.2
Ruzzon, E.3
Zanon, E.4
Girolami, B.5
-
3
-
-
12344313430
-
Thrombotic complications in patients with hereditary bleeding disorders
-
Franchini M. Thrombotic complications in patients with hereditary bleeding disorders. Thromb Haemost 2004; 92: 298-304.
-
(2004)
Thromb Haemost
, vol.92
, pp. 298-304
-
-
Franchini, M.1
-
4
-
-
0035669048
-
Factor IX and thrombosis
-
Lowe GD. Factor IX and thrombosis. Brit JHaematol 2001; 115: 507-13.
-
(2001)
Brit JHaematol
, vol.115
, pp. 507-513
-
-
Lowe, G.D.1
-
5
-
-
33645875295
-
Arterial and venous thrombosis in patients with von Willebrand disease
-
Girolami A, Tezza F, Scapin M, Vettore S, Casonato S. Arterial and venous thrombosis in patients with von Willebrand disease. J. Thromb Thromboly 2006; 21: 175-8.
-
(2006)
J. Thromb Thromboly
, vol.21
, pp. 175-178
-
-
Girolami, A.1
Tezza, F.2
Scapin, M.3
Vettore, S.4
Casonato, S.5
-
6
-
-
0025439210
-
Gastrectomy for a patient with congenital factor VII deficiency-a case report]
-
Nakagawa K, Furusawa A, Momono S, Sasaki Y, Ujiie K. Gastrectomy for a patient with congenital factor VII deficiency-a case report]. Nippon Geka Gakkai Zasshi 1990; 91: 771-3.
-
(1990)
Nippon Geka Gakkai Zasshi
, vol.91
, pp. 771-773
-
-
Nakagawa, K.1
Furusawa, A.2
Momono, S.3
Sasaki, Y.4
Ujiie, K.5
-
7
-
-
0018192517
-
Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern
-
Girolami A, Fabris F, Dal Bo Zanon R, Ghiotto G, Burul A. Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern. J Lab Clin Med 1978; 91: 387-95.
-
(1978)
J Lab Clin Med
, vol.91
, pp. 387-395
-
-
Girolami, A.1
Fabris, F.2
Dal Bo Zanon, R.3
Ghiotto, G.4
Burul, A.5
-
8
-
-
0000909239
-
A clinical and family study of hereditary proconvertin (factor VII) deficiency
-
Hall CA, Rapaport SI, Ames SB, Degroot JA. A clinical and family study of hereditary proconvertin (factor VII) deficiency. Am J Med 1964; 37: 172-81.
-
(1964)
Am J Med
, vol.37
, pp. 172-181
-
-
Hall, C.A.1
Rapaport, S.I.2
Ames, S.B.3
Degroot, J.A.4
-
10
-
-
0031711654
-
Development of a subdural vein thrombosis following aggressive factor VII replacement for postnatal intracranial haemorrhage in a homozygous factor VII-deficient infant
-
Worth LL, Hoots WK. Development of a subdural vein thrombosis following aggressive factor VII replacement for postnatal intracranial haemorrhage in a homozygous factor VII-deficient infant. Haemophilia 1998; 4: 757-61.
-
(1998)
Haemophilia
, vol.4
, pp. 757-761
-
-
Worth, L.L.1
Hoots, W.K.2
-
11
-
-
0020565895
-
Thrombosis or myocardial infarction 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 infarction in congenital clotting factor abnormalities and chronic thrombocytopenias: a report of 21 patients and a review of 50 previously reported cases. Medicine 1983; 62: 248-55.
-
(1983)
Medicine
, vol.62
, pp. 248-255
-
-
Goodnough, L.T.1
Saito, H.2
Ratnoff, O.D.3
-
12
-
-
0029166576
-
Severe hypofibrinogenemia associated with bilateral ischemic necrosis of toes and fingers
-
Chafa O, Chellali T, Sternberg C, Reghis A, Hamladji RM, Fischer AM. Severe hypofibrinogenemia associated with bilateral ischemic necrosis of toes and fingers. Blood Coagul Fibrinoly 1995; 6: 549-52.
-
(1995)
Blood Coagul Fibrinoly
, vol.6
, pp. 549-552
-
-
Chafa, O.1
Chellali, T.2
Sternberg, C.3
Reghis, A.4
Hamladji, R.M.5
Fischer, A.M.6
-
13
-
-
0023841155
-
Multiple pulmonary emboli in a patient with afibrinogenaemia
-
Cronin C, Fitzpatrick D, Temperley I. Multiple pulmonary emboli in a patient with afibrinogenaemia. Acta Haematol 1988; 79: 53-4.
-
(1988)
Acta Haematol
, vol.79
, pp. 53-54
-
-
Cronin, C.1
Fitzpatrick, D.2
Temperley, I.3
-
14
-
-
0027325571
-
Association of congenital afibrinogenemia and K-dependent protein C deficiency - a case report
-
de Mattia D, Regina G, Giordano P, Del Vecchio GC, Altomare M, Schettini F. Association of congenital afibrinogenemia and K-dependent protein C deficiency - a case report. Angiology 1993; 44: 745-9.
-
(1993)
Angiology
, vol.44
, pp. 745-749
-
-
de Mattia, D.1
Regina, G.2
Giordano, P.3
Del Vecchio, G.C.4
Altomare, M.5
Schettini, F.6
-
15
-
-
0001714190
-
Precipitating antifibrinogen antibody appearing after fibrinogen infusions in a patient with congenital afibrinogenemia
-
de Vries A, Rosenberg T, Kochwa S, Boss JH. Precipitating antifibrinogen antibody appearing after fibrinogen infusions in a patient with congenital afibrinogenemia. Am J Med 1961; 30: 486-94.
-
(1961)
Am J Med
, vol.30
, pp. 486-494
-
-
de Vries, A.1
Rosenberg, T.2
Kochwa, S.3
Boss, J.H.4
-
16
-
-
0027119321
-
Portal vein thrombosis revealing congenital afibrinogenemia
-
Drai E, Taillan B, Schneider S, Ferrari E, Bayle J, Dujardin P. Portal vein thrombosis revealing congenital afibrinogenemia. Presse Med 1992; 21: 1820-1.
-
(1992)
Presse Med
, vol.21
, pp. 1820-1821
-
-
Drai, E.1
Taillan, B.2
Schneider, S.3
Ferrari, E.4
Bayle, J.5
Dujardin, P.6
-
17
-
-
0035341028
-
Embolized ischemic lesions of toes in an afibrinogenemic patient: possible relevance to in vivo circulating thrombin
-
Dupuy E, Soria C, Molho P et al. Embolized ischemic lesions of toes in an afibrinogenemic patient: possible relevance to in vivo circulating thrombin. Thromb Res 2001; 102: 211-19.
-
(2001)
Thromb Res
, vol.102
, pp. 211-219
-
-
Dupuy, E.1
Soria, C.2
Molho, P.3
-
18
-
-
0030464689
-
Bilateral vertebral artery dissection in a patient with afibrinogenemia
-
Garcia-Monco JC, Fernandez Canton G, Gomez Beldarrain M. Bilateral vertebral artery dissection in a patient with afibrinogenemia. Stroke 1996; 27: 2325-2327.
-
(1996)
Stroke
, vol.27
, pp. 2325-2327
-
-
Garcia-Monco, J.C.1
Fernandez Canton, G.2
Gomez Beldarrain, M.3
-
19
-
-
0026712995
-
Coexistence of congenital afibrinogenemia and protein C deficiency in a patient
-
Hanano M, Takahashi H, Itoh M, Shibata A. Coexistence of congenital afibrinogenemia and protein C deficiency in a patient. Am J Hematol 1992; 41: 57-60.
-
(1992)
Am J Hematol
, vol.41
, pp. 57-60
-
-
Hanano, M.1
Takahashi, H.2
Itoh, M.3
Shibata, A.4
-
20
-
-
0013873787
-
Fatal pulmonary embolus in congenital fibrinopenia. Report of two cases
-
Ingram GI, McBrien DJ, Spencer H. Fatal pulmonary embolus in congenital fibrinopenia. Report of two cases. Acta Haematol 1966; 35: 56-62.
-
(1966)
Acta Haematol
, vol.35
, pp. 56-62
-
-
Ingram, G.I.1
McBrien, D.J.2
Spencer, H.3
-
21
-
-
0343603909
-
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia
-
Lak M, Keihani M, Elahi F, Peyvandi F, Mannucci PM. Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia. Br J Haematol 1999; 107: 204-6.
-
(1999)
Br J Haematol
, vol.107
, pp. 204-206
-
-
Lak, M.1
Keihani, M.2
Elahi, F.3
Peyvandi, F.4
Mannucci, P.M.5
-
22
-
-
0015208908
-
Congenital afibrinogenemia
-
MacKinnon HH, Fekete JF. Congenital afibrinogenemia. Vascular changes and multiple thromboses induced by fibrinogen infusions and contraceptive medication. Can Med Assoc J 1971; 104: 597-9.
-
(1971)
Can Med Assoc J
, vol.104
, pp. 597-599
-
-
MacKinnon, H.H.1
Fekete, J.F.2
-
23
-
-
0005424293
-
Fibrinogen-indipendent platelet aggregation responsible of arterial thrombosis in an afibrinogemic patient
-
Molho-Sabatier P, Soria C, Legrand Ch et al. Fibrinogen-indipendent platelet aggregation responsible of arterial thrombosis in an afibrinogemic patient. Thromb Haemost 1991; 65: 850.
-
(1991)
Thromb Haemost
, vol.65
, pp. 850
-
-
Molho-Sabatier, P.1
Soria, C.2
Legrand, C.3
-
24
-
-
84873299384
-
Some observation on the blood clotting mechanism
-
Pinninger IL, Prunty FT. Some observation on the blood clotting mechanism. The role of fibrinogen and platelets with reference to a case of congenital afibrinogenemia. Brit J Exp Pathol 1946; 27: 20-6.
-
(1946)
Brit J Exp Pathol
, vol.27
, pp. 20-26
-
-
Pinninger, I.L.1
Prunty, F.T.2
-
25
-
-
2442529557
-
Lepirudin therapy for thrombotic complications in congenital afibrinogenaemia
-
Schuepbach RA, Meili EO, Schneider E, Peter U, Bachli EB. Lepirudin therapy for thrombotic complications in congenital afibrinogenaemia. Thromb Haemost 2004; 91: 1044-6.
-
(2004)
Thromb Haemost
, vol.91
, pp. 1044-1046
-
-
Schuepbach, R.A.1
Meili, E.O.2
Schneider, E.3
Peter, U.4
Bachli, E.B.5
-
26
-
-
11844300363
-
Mesenteric venous thrombosis in a patient with congenital afibrinogenemia and diffuse peritonitis
-
Takasugi Y, Shiokawa Y, Kajikawa R et al. Mesenteric venous thrombosis in a patient with congenital afibrinogenemia and diffuse peritonitis. Ann Hematol 2005; 84: 129-30.
-
(2005)
Ann Hematol
, vol.84
, pp. 129-130
-
-
Takasugi, Y.1
Shiokawa, Y.2
Kajikawa, R.3
-
27
-
-
0028880394
-
Severe arterial thrombosis in a congenitally factor VII deficient patient
-
Escoffre M, Zini JM, Schliamser L et al. Severe arterial thrombosis in a congenitally factor VII deficient patient. Br J Haematol 1995; 91: 739-41.
-
(1995)
Br J Haematol
, vol.91
, pp. 739-741
-
-
Escoffre, M.1
Zini, J.M.2
Schliamser, L.3
-
28
-
-
0026056520
-
Thrombotic complications after substitution with a FVII concentrate
-
Schulman S, Johnsson H, Lindmarker P. Thrombotic complications after substitution with a FVII concentrate. Thromb Haemost 1991; 66: 619.
-
(1991)
Thromb Haemost
, vol.66
, pp. 619
-
-
Schulman, S.1
Johnsson, H.2
Lindmarker, P.3
-
29
-
-
0015928913
-
Deep vein thrombosis and pulmonary embolism in congenital factor VII deficiency
-
Gershwin ME, Gude JK. Deep vein thrombosis and pulmonary embolism in congenital factor VII deficiency. N Engl J Med 1973; 288: 141-2.
-
(1973)
N Engl J Med
, vol.288
, pp. 141-142
-
-
Gershwin, M.E.1
Gude, J.K.2
-
30
-
-
0021341369
-
Thromboembolism in congenital factor VII deficiency
-
Shifter T, Machtey I, Creter D. Thromboembolism in congenital factor VII deficiency. Acta Haematol 1984; 71: 60-2.
-
(1984)
Acta Haematol
, vol.71
, pp. 60-62
-
-
Shifter, T.1
Machtey, I.2
Creter, D.3
-
31
-
-
0014695362
-
Congenital factor VII deficiency Two cases in children of cousins
-
Heikinheimo R, Reinikainen M. Congenital factor VII deficiency. Two cases in children of cousins. Thromb Diath Haemorrh 1969; 21: 245-8.
-
(1969)
Thromb Diath Haemorrh
, vol.21
, pp. 245-248
-
-
Heikinheimo, R.1
Reinikainen, M.2
-
32
-
-
0019184214
-
Thromboembolism in patients with hereditary deficiency of coagulation factors
-
Solanki DL, Corn M. Thromboembolism in patients with hereditary deficiency of coagulation factors. South Med J 1980; 73: 944-6.
-
(1980)
South Med J
, vol.73
, pp. 944-946
-
-
Solanki, D.L.1
Corn, M.2
-
33
-
-
0022353665
-
Congenital factor VII deficiency and cerebrovascular stroke
-
Lefrere JJ, Chaunu MP, Conard J, Horellou MH, Samama M. Congenital factor VII deficiency and cerebrovascular stroke. Lancet 1985; 2: 1006-7.
-
(1985)
Lancet
, vol.2
, pp. 1006-1007
-
-
Lefrere, J.J.1
Chaunu, M.P.2
Conard, J.3
Horellou, M.H.4
Samama, M.5
-
34
-
-
0016854163
-
Pulmonary embolism with factor XI deficiency
-
Brodsky JB, Burgess GE. Pulmonary embolism with factor XI deficiency. JAMA 1975; 234: 1156-7.
-
(1975)
JAMA
, vol.234
, pp. 1156-1157
-
-
Brodsky, J.B.1
Burgess, G.E.2
-
35
-
-
4444317749
-
A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiency
-
Bolton-Maggs PH, Peretz H, Butler R et al. A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiency. J Thromb Haemost 2004; 2: 918-24.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 918-924
-
-
Bolton-Maggs, P.H.1
Peretz, H.2
Butler, R.3
-
36
-
-
0014291990
-
[A case of congenital factor XI (plasma thromboplastin antecedent) deficiency with large organized thrombus in the vena cava inferior]
-
Umeda T, Hiramaru M, Nishino T, Onchi K, Matsuda T. [A case of congenital factor XI (plasma thromboplastin antecedent) deficiency with large organized thrombus in the vena cava inferior]. Acta Hemat Jpn 1968; 31: 325-33.
-
(1968)
Acta Hemat Jpn
, vol.31
, pp. 325-333
-
-
Umeda, T.1
Hiramaru, M.2
Nishino, T.3
Onchi, K.4
Matsuda, T.5
-
37
-
-
0027977953
-
Thrombogenic potential of factor XI concentrate
-
Bolton-Maggs PH, Colvin BT, Satchi BT, Lee CA, Lucas GS. Thrombogenic potential of factor XI concentrate. Lancet 1994; 344: 748-9.
-
(1994)
Lancet
, vol.344
, pp. 748-749
-
-
Bolton-Maggs, P.H.1
Colvin, B.T.2
Satchi, B.T.3
Lee, C.A.4
Lucas, G.S.5
-
38
-
-
0025740864
-
Myocardial infarction in a patient with factor XI deficiency and a lupus anticoagulant
-
Humphries JE, Schlein AE, Sarembock IJ, Gonias SL. Myocardial infarction in a patient with factor XI deficiency and a lupus anticoagulant. Eur Heart J 1991; 12: 1045-7.
-
(1991)
Eur Heart J
, vol.12
, pp. 1045-1047
-
-
Humphries, J.E.1
Schlein, A.E.2
Sarembock, I.J.3
Gonias, S.L.4
-
39
-
-
0032408233
-
Thromboembolic phenomena in patients with hereditary factor XI deficiency
-
Sherer Y, Bar-Zohar D, Levy Y, Shoenfeld Y. Thromboembolic phenomena in patients with hereditary factor XI deficiency. Ann Med Interne 1998; 149: 492-4.
-
(1998)
Ann Med Interne
, vol.149
, pp. 492-494
-
-
Sherer, Y.1
Bar-Zohar, D.2
Levy, Y.3
Shoenfeld, Y.4
-
40
-
-
0030707875
-
Recurrent venous thromboembolic disease and factor XI concentrate in a patient with severe factor XI deficiency, chronic myelomonocytic leukaemia, factor V Leiden and heterozygous plasminogen deficiency
-
Evans G, Pasi KJ, Mehta A, Lee CA, Perry DJ. Recurrent venous thromboembolic disease and factor XI concentrate in a patient with severe factor XI deficiency, chronic myelomonocytic leukaemia, factor V Leiden and heterozygous plasminogen deficiency. Blood Coagul Fibrinoly 1997; 8: 437-40.
-
(1997)
Blood Coagul Fibrinoly
, vol.8
, pp. 437-440
-
-
Evans, G.1
Pasi, K.J.2
Mehta, A.3
Lee, C.A.4
Perry, D.J.5
-
41
-
-
0842268250
-
Clinical experience of a FXI concentrate: possible side effects
-
Gitel SN, Veron D, Schulman S. Clinical experience of a FXI concentrate: possible side effects. Thromb Haemost 1991; 65: 1157.
-
(1991)
Thromb Haemost
, vol.65
, pp. 1157
-
-
Gitel, S.N.1
Veron, D.2
Schulman, S.3
-
42
-
-
0142197166
-
Inherited factor XI deficiency confers no protection against acute myocardial infarction
-
Salomon O, Steinberg DM, Dardik R et al. Inherited factor XI deficiency confers no protection against acute myocardial infarction. J Thromb Haemost 2003, 1: 658-61.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 658-661
-
-
Salomon, O.1
Steinberg, D.M.2
Dardik, R.3
-
43
-
-
76949126204
-
Factor V deficiency in hemorrhagic diathesis
-
Cosgriff W, Leifer E. Factor V deficiency in hemorrhagic diathesis. JAMA 1952; 148: 462-464.
-
(1952)
JAMA
, vol.148
, pp. 462-464
-
-
Cosgriff, W.1
Leifer, E.2
-
44
-
-
0024306895
-
Thromboembolic manifestations and congenital factor V deficiency: a family study
-
Manotti C, Quintavalla R, Pini M, Jeran M, Paolicelli M, Dettori AG. Thromboembolic manifestations and congenital factor V deficiency: a family study. Haemostasis 1989; 19: 331-4.
-
(1989)
Haemostasis
, vol.19
, pp. 331-334
-
-
Manotti, C.1
Quintavalla, R.2
Pini, M.3
Jeran, M.4
Paolicelli, M.5
Dettori, A.G.6
-
45
-
-
9444275762
-
Coagulation dynamics in factor V deficiency: a family study with a note on the occurrence of thrombophlebitis
-
Miller SP. Coagulation dynamics in factor V deficiency: a family study with a note on the occurrence of thrombophlebitis. Thromb Diath Haemorrh 1965; 13: 500-15.
-
(1965)
Thromb Diath Haemorrh
, vol.13
, pp. 500-515
-
-
Miller, S.P.1
-
46
-
-
0017284969
-
Recurrent thrombophlebitis and pulmonary embolism in congenital FV deficiency
-
Reich NE, Hoffman GL, De Wolfe VG. Recurrent thrombophlebitis and pulmonary embolism in congenital FV deficiency. Chest 1976; 69: 113-14.
-
(1976)
Chest
, vol.69
, pp. 113-114
-
-
Reich, N.E.1
Hoffman, G.L.2
De Wolfe, V.G.3
-
48
-
-
0028122941
-
Activation of the coagulation cascade after infusion of a factor XI concentrate in congenitally deficient patients
-
Mannucci PM, Bauer KA, Santagostino E et al. Activation of the coagulation cascade after infusion of a factor XI concentrate in congenitally deficient patients. Blood 1994; 84: 1314-19.
-
(1994)
Blood
, vol.84
, pp. 1314-1319
-
-
Mannucci, P.M.1
Bauer, K.A.2
Santagostino, E.3
-
49
-
-
0031743980
-
Congenital deficiencies and abnormalities of prothrombin
-
Girolami A, Scarano L, Saggiorato G, Girolami B, Bertomoro A, Marchiori A. Congenital deficiencies and abnormalities of prothrombin. Blood Coagul Fibrinoly 1998; 9: 557-69.
-
(1998)
Blood Coagul Fibrinoly
, vol.9
, pp. 557-569
-
-
Girolami, A.1
Scarano, L.2
Saggiorato, G.3
Girolami, B.4
Bertomoro, A.5
Marchiori, A.6
-
50
-
-
84873299717
-
La deficienza congenita del FX (fattore Stuart-Prower) progr
-
Girolami A, Cella G, Borsato N, Burul A, Zucchetto M, Cafiero F. La deficienza congenita del FX (fattore Stuart-Prower) progr. Medicine 1975; 31: 1-15.
-
(1975)
Medicine
, vol.31
, pp. 1-15
-
-
Girolami, A.1
Cella, G.2
Borsato, N.3
Burul, A.4
Zucchetto, M.5
Cafiero, F.6
-
51
-
-
0030804838
-
Inherited factor X deficiency: molecular genetics and pathophysiology
-
Cooper DN, Millar DS, Wacey A, Pemberton S, Tuddenham EG. Inherited factor X deficiency: molecular genetics and pathophysiology. Thromb Haemost 1997; 78: 161-72.
-
(1997)
Thromb Haemost
, vol.78
, pp. 161-172
-
-
Cooper, D.N.1
Millar, D.S.2
Wacey, A.3
Pemberton, S.4
Tuddenham, E.G.5
-
52
-
-
13844298983
-
Unusual longevity in a patient with factor X Friuli coagulation disorder
-
Girolami A, Randi ML, Tezza F, Molaro G, Girolami B. Unusual longevity in a patient with factor X Friuli coagulation disorder. Thromb Haemost 2005; 93: 385-7.
-
(2005)
Thromb Haemost
, vol.93
, pp. 385-387
-
-
Girolami, A.1
Randi, M.L.2
Tezza, F.3
Molaro, G.4
Girolami, B.5
-
53
-
-
0016736708
-
Factor X Friuli coagulation disorder The demise of the index patient
-
Girolami A, Molaro G, Falomo R. Factor X Friuli coagulation disorder. The demise of the index patient. Acta Haematol 1975; 54: 120-5.
-
(1975)
Acta Haematol
, vol.54
, pp. 120-125
-
-
Girolami, A.1
Molaro, G.2
Falomo, R.3
-
54
-
-
0026056520
-
Thrombotic complications after substitution with a FVII concentrate
-
Schulman S, Johnsson H, Lindmarker P. Thrombotic complications after substitution with a FVII concentrate. Thromb Haemost 1991; 66: 619.
-
(1991)
Thromb Haemost
, vol.66
, pp. 619
-
-
Schulman, S.1
Johnsson, H.2
Lindmarker, P.3
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