-
2
-
-
0021799672
-
Rare quantitative and qualitative abnormalities of coagulation
-
Girolami A, De Marco L, Dal Bo Zanon R, Patrassi G, Cappellato MG. Rare quantitative and qualitative abnormalities of coagulation. Clin Haematol 1985; 14: 385-411.
-
(1985)
Clin Haematol
, vol.14
, pp. 385-411
-
-
Girolami, A.1
De Marco, L.2
Dal Bo Zanon, R.3
Patrassi, G.4
Cappellato, M.G.5
-
3
-
-
0011967027
-
Hemophilia in Iran
-
Ala F, Denson KWE, eds. Excerpta Medica
-
Shoa'i I, Ala F, Forouzanfar N. Hemophilia in Iran. In: Haemophilia. Ala F, Denson KWE, eds. Excerpta Medica, 1973, pp XII-XV.
-
(1973)
Haemophilia
-
-
Shoa'i, I.1
Ala, F.2
Forouzanfar, N.3
-
4
-
-
0013638141
-
Molecular characterization of 22 families with factor VII deficiency
-
Peyvandi F, Mannucci PM, Jenkins PV, Lee A, Pasi KJ, Coppola R, Perry DL. Molecular characterization of 22 families with factor VII deficiency. Blood 1998; 92 (suppl. 1): 711a.
-
(1998)
Blood
, vol.92
, Issue.SUPPL. 1
-
-
Peyvandi, F.1
Mannucci, P.M.2
Jenkins, P.V.3
Lee, A.4
Pasi, K.J.5
Coppola, R.6
Perry, D.L.7
-
5
-
-
0033120708
-
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency (F5F8D)
-
Neerman-Arbez M, Johnson KM, Morris MA, McVey JH, Peyvandi F, Nichols WC, Ginshurg D, Rossier C. Antonarakis SE, Tuddenham EGD. Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency (F5F8D). Blood, 1999; 93: 2253-60.
-
(1999)
Blood
, vol.93
, pp. 2253-2260
-
-
Neerman-Arbez, M.1
Johnson, K.M.2
Morris, M.A.3
McVey, J.H.4
Peyvandi, F.5
Nichols, W.C.6
Ginshurg, D.7
Rossier, C.8
Antonarakis, S.E.9
Tuddenham, E.G.D.10
-
6
-
-
0344355731
-
Molecular characterization of 11 kindreds with prothrombin deficiency
-
abstr. no. 50
-
Akhavan S, Lak M. Mancuso G, Baudo F. Rocino A, Mazzucconi MG, Perkins SJ, Mannucci PM. Molecular characterization of 11 kindreds with prothrombin deficiency. Thromb Haemost 1999; 82 (Suppl.-Abstracts): 17 (abstr. no. 50).
-
(1999)
Thromb Haemost
, vol.82
, Issue.SUPPL.-ABSTRACTS
, pp. 17
-
-
Akhavan, S.1
Lak, M.2
Mancuso, G.3
Baudo, F.4
Rocino, A.5
Mazzucconi, M.G.6
Perkins, S.J.7
Mannucci, P.M.8
-
7
-
-
0345650245
-
First identification of a missense mutation in the D-domain of the fibrinogen beta chain in a case of congenital afibrinogenemia
-
abstr. no. 52
-
Duga S, Asselta R, Simonie T, Santagostino E, Mannucci PM, Malcovati M, Tenchini ML. First identification of a missense mutation in the D-domain of the fibrinogen beta chain in a case of congenital afibrinogenemia. Thromb Haemost 1999; 82 (Suppl.-Abstracts): 18 (abstr. no. 52).
-
(1999)
Thromb Haemost
, vol.82
, Issue.SUPPL.-ABSTRACTS
, pp. 18
-
-
Duga, S.1
Asselta, R.2
Simonie, T.3
Santagostino, E.4
Mannucci, P.M.5
Malcovati, M.6
Tenchini, M.L.7
-
8
-
-
0344787560
-
Other clotting factor deficiencies
-
RW Colman, Hirsh J, Marder VJ, Salzman EW, eds. J. B. Lippincott Company, Philadelphia, in press
-
Roberts HR. Hoffman M. Other clotting factor deficiencies. In: Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 4th edition. RW Colman, Hirsh J, Marder VJ, Salzman EW, eds. J. B. Lippincott Company, Philadelphia, 1999: in press.
-
(1999)
Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 4th Edition
-
-
Roberts, H.R.1
Hoffman, M.2
-
9
-
-
0002496721
-
Other coagulation factor deficiencies
-
J Loscalzo, AL Schafer, eds. Williams and Wilkins, Baltimore
-
nd edition. J Loscalzo, AL Schafer, eds. Williams and Wilkins, Baltimore, 1998, pp 773-802.
-
(1998)
nd Edition
, pp. 773-802
-
-
Roberts, H.R.1
Bingham, M.D.2
-
10
-
-
0020552654
-
Factor VII congenital deficiency: Clinical picture and classification of the variants
-
Mariani G, Mazzucconi MG. Factor VII congenital deficiency: clinical picture and classification of the variants. Haemostasis 1983; 13: 169-74.
-
(1983)
Haemostasis
, vol.13
, pp. 169-174
-
-
Mariani, G.1
Mazzucconi, M.G.2
-
11
-
-
0032924251
-
Deletion of the fibrinogen alpha chain gene (FGA) causes congenital afibrinogenemia
-
Neerman-Arbez M. Honsherg A, Antonorakis SE, Morris MA. Deletion of the fibrinogen alpha chain gene (FGA) causes congenital afibrinogenemia. J Clin Invest 1999; 103: 215-8.
-
(1999)
J Clin Invest
, vol.103
, pp. 215-218
-
-
Neerman-Arbez, M.1
Honsherg, A.2
Antonorakis, S.E.3
Morris, M.A.4
-
12
-
-
0030799318
-
Congenital dysfibrinogenemia
-
Martinez J. Congenital dysfibrinogenemia. Curr Opin Hematol 1997; 4: 357-65.
-
(1997)
Curr Opin Hematol
, vol.4
, pp. 357-365
-
-
Martinez, J.1
-
13
-
-
0029147959
-
Resolution of spontaneous bleeding events but failure of pregnancy in fibrinogen deficient mice
-
Suh TT, Holmback K, Jensen NJ, Daugherty CC, Small K, Simon DI, Potter S, Degen JL. Resolution of spontaneous bleeding events but failure of pregnancy in fibrinogen deficient mice. Genes Dev 1995: 15: 2020-33.
-
(1995)
Genes Dev
, vol.15
, pp. 2020-2033
-
-
Suh, T.T.1
Holmback, K.2
Jensen, N.J.3
Daugherty, C.C.4
Small, K.5
Simon, D.I.6
Potter, S.7
Degen, J.L.8
-
14
-
-
0024533298
-
Congenital hypofibrinogenemia in pregnancy
-
Goodwin TM. Congenital hypofibrinogenemia in pregnancy. Obstet Gynecol Surv 1989: 44: 157-61.
-
(1989)
Obstet Gynecol Surv
, vol.44
, pp. 157-161
-
-
Goodwin, T.M.1
-
16
-
-
0017376280
-
Afibrinogenemia with intracerebral hematoma. Report in a successfully treated case
-
Montgomery R, Natelson SE. Afibrinogenemia with intracerebral hematoma. Report in a successfully treated case. Am J Dis Child 1977; 131: 555-6.
-
(1977)
Am J Dis Child
, vol.131
, pp. 555-556
-
-
Montgomery, R.1
Natelson, S.E.2
-
17
-
-
0018887670
-
Congenital afibrinogenemia in 10 offspring of uncle-niece marriages
-
Fried K, Kaufman S. Congenital afibrinogenemia in 10 offspring of uncle-niece marriages. Clin Genet 1980; 18: 223-7.
-
(1980)
Clin Genet
, vol.18
, pp. 223-227
-
-
Fried, K.1
Kaufman, S.2
-
18
-
-
0031938607
-
Current status of solvent/detergent treated frozen plasma
-
Klein HG, Dodd RY, Dzik WH, Luban NL, Ness PM, Pisciotto P, Schiff PD, Snyder EL. Current status of solvent/detergent treated frozen plasma. Transfusion 1998; 38: 102-7.
-
(1998)
Transfusion
, vol.38
, pp. 102-107
-
-
Klein, H.G.1
Dodd, R.Y.2
Dzik, W.H.3
Luban, N.L.4
Ness, P.M.5
Pisciotto, P.6
Schiff, P.D.7
Snyder, E.L.8
-
19
-
-
0030013848
-
The choice of plasma derived clotting factor concentrates
-
C.A. Lee, editor
-
Mannucci PM, The choice of plasma derived clotting factor concentrates. In: Balliere's Clinical Haematology. Haemophilia, (C.A. Lee, editor) 1996; 9: 272-90.
-
(1996)
Balliere's Clinical Haematology. Haemophilia
, vol.9
, pp. 272-290
-
-
Mannucci, P.M.1
-
20
-
-
0025893790
-
Photoinactivation of viruses in human fresh plasma by phenothiazine dyes in combination with visible light
-
Lambrecht B, Mohr H, Knouwerhoft J, Schmitt H. Photoinactivation of viruses in human fresh plasma by phenothiazine dyes in combination with visible light. Vox Sang 1991; 60: 207-13.
-
(1991)
Vox Sang
, vol.60
, pp. 207-213
-
-
Lambrecht, B.1
Mohr, H.2
Knouwerhoft, J.3
Schmitt, H.4
-
21
-
-
0032560553
-
Prothrombin deficiency results in embryonic and neonatal lethality in mice
-
Sun WY, Witte DP, Degen JL, Colben MC, Holmback K, Xiao Q, Bugge TH, Degen SJ. Prothrombin deficiency results in embryonic and neonatal lethality in mice. Proc. Natl Acad Sci USA 1998; 95: 7597-8002.
-
(1998)
Proc. Natl Acad Sci USA
, vol.95
, pp. 7597-8002
-
-
Sun, W.Y.1
Witte, D.P.2
Degen, J.L.3
Colben, M.C.4
Holmback, K.5
Xiao, Q.6
Bugge, T.H.7
Degen, S.J.8
-
22
-
-
0020590736
-
Heterogeneity of human factor V deficiency. Evidence for the existence of an antigen-positive variant
-
Chiu HC, Whitaker E, Colman RW. Heterogeneity of human factor V deficiency. Evidence for the existence of an antigen-positive variant. J Clin Invest 1983: 72: 493-503.
-
(1983)
J Clin Invest
, vol.72
, pp. 493-503
-
-
Chiu, H.C.1
Whitaker, E.2
Colman, R.W.3
-
23
-
-
0019977242
-
Radioimmunoassay of factor V in human plasma and platelets
-
Tracy PB, Eide LL, Bowie EJ, Mann KG. Radioimmunoassay of factor V in human plasma and platelets. Blood 1982; 60: 59-63.
-
(1982)
Blood
, vol.60
, pp. 59-63
-
-
Tracy, P.B.1
Eide, L.L.2
Bowie, E.J.3
Mann, K.G.4
-
25
-
-
0032529497
-
A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject
-
Lunghi B, Castoldi E, Mingozzi F, Bernardi F. A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject. Blood 1998; 92: 1463-4.
-
(1998)
Blood
, vol.92
, pp. 1463-1464
-
-
Lunghi, B.1
Castoldi, E.2
Mingozzi, F.3
Bernardi, F.4
-
26
-
-
0032847937
-
Familial coagulation factor V deficiency caused by a novel 4 base pair insertion in the factor V gene
-
in press
-
Zehender JL, Hiraki D, Jones C, Gross N, Grumet FC. Familial coagulation factor V deficiency caused by a novel 4 base pair insertion in the factor V gene. Thromb Haemost 1999: in press.
-
(1999)
Thromb Haemost
-
-
Zehender, J.L.1
Hiraki, D.2
Jones, C.3
Gross, N.4
Grumet, F.C.5
-
27
-
-
0031968129
-
Severe coagulation factor V deficiency caused by a 4 bp deletion in the factor V gene
-
Guasch JF, Cannegieler S, Reitsma PH, Van't Veer-Korthof ET, Bertina RM. Severe coagulation factor V deficiency caused by a 4 bp deletion in the factor V gene. Br J Haematol 1998; 101: 32-9.
-
(1998)
Br J Haematol
, vol.101
, pp. 32-39
-
-
Guasch, J.F.1
Cannegieler, S.2
Reitsma, P.H.3
Van't Veer-Korthof, E.T.4
Bertina, R.M.5
-
28
-
-
0029854371
-
Fatal hemorrhage and incomplete block of embryogenesis in mice lacking coagulation factor V
-
Cui J, O'Shea KS, Purkayastha A, Saunders TL, Ginsburg D. Fatal hemorrhage and incomplete block of embryogenesis in mice lacking coagulation factor V. Nature 1996; 384: 66-8.
-
(1996)
Nature
, vol.384
, pp. 66-68
-
-
Cui, J.1
O'Shea, K.S.2
Purkayastha, A.3
Saunders, T.L.4
Ginsburg, D.5
-
29
-
-
0033978610
-
Rescue of fatal neonatal hemorrhage in factor V deficient mice by low transgene expression
-
in press
-
Yang TL, Cui J, Taylor JM, Yang A, Gimber SB, Ginsburg D. Rescue of fatal neonatal hemorrhage in factor V deficient mice by low transgene expression. Thromb Haemost 1999; in press.
-
(1999)
Thromb Haemost
-
-
Yang, T.L.1
Cui, J.2
Taylor, J.M.3
Yang, A.4
Gimber, S.B.5
Ginsburg, D.6
-
30
-
-
0032442129
-
Symptoms of inherited factor V deficiency in 25 Iranian patients
-
Lak M, Sharifian R, Peyvandi F, Mannucci PM. Symptoms of inherited factor V deficiency in 25 Iranian patients. Br J Haematol 1998; 103: 1067-9.
-
(1998)
Br J Haematol
, vol.103
, pp. 1067-1069
-
-
Lak, M.1
Sharifian, R.2
Peyvandi, F.3
Mannucci, P.M.4
-
31
-
-
0022410305
-
Hereditary factor VII deficiency heterogeneity defined by combined functional and immunochemical analysis
-
Triplett DA, Brandt JT, Batard MA, Dixon JL, Fair DS. Hereditary factor VII deficiency heterogeneity defined by combined functional and immunochemical analysis. Blood 1985; 66: 1284-7.
-
(1985)
Blood
, vol.66
, pp. 1284-1287
-
-
Triplett, D.A.1
Brandt, J.T.2
Batard, M.A.3
Dixon, J.L.4
Fair, D.S.5
-
32
-
-
0030813937
-
Inherited factor VII deficiency: Molecular genetics and pathophysiology
-
Cooper DN, Millar DS, Wacey A, Banner DW, Tuddenham EGD. Inherited factor VII deficiency: molecular genetics and pathophysiology. Thromb Haemost 1997; 78:151-60.
-
(1997)
Thromb Haemost
, vol.78
, pp. 151-160
-
-
Cooper, D.N.1
Millar, D.S.2
Wacey, A.3
Banner, D.W.4
Tuddenham, E.G.D.5
-
33
-
-
0030775316
-
Mice lacking factor VII develop normally but suffer fatal perinatal bleeding
-
Rosen ED, Chan JC, Idusogie E, Clotman F, Vlasuk G, Luther T, Jalbert LR, Albrecht S, Zhong L, Lissens A, Schoonjans L, Moons L, Collen D, Castellino FJ, Carmeliet P. Mice lacking factor VII develop normally but suffer fatal perinatal bleeding. Nature 1997; 390: 290-4.
-
(1997)
Nature
, vol.390
, pp. 290-294
-
-
Rosen, E.D.1
Chan, J.C.2
Idusogie, E.3
Clotman, F.4
Vlasuk, G.5
Luther, T.6
Jalbert, L.R.7
Albrecht, S.8
Zhong, L.9
Lissens, A.10
Schoonjans, L.11
Moons, L.12
Collen, D.13
Castellino, F.J.14
Carmeliet, P.15
-
34
-
-
0344355727
-
Clinical aspects of congenital factor VII deficiency
-
Marder VJ, Shulman NR. Clinical aspects of congenital factor VII deficiency. Blut 1979; 30: 119-25.
-
(1979)
Blut
, vol.30
, pp. 119-125
-
-
Marder, V.J.1
Shulman, N.R.2
-
35
-
-
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
-
37
-
-
0027522777
-
Recombinant activated factor VII in the treatment of bleeding episodes in individuals with inherited and acquired bleeding disorders
-
Hedner U, Glazer S, Falch J. Recombinant activated factor VII in the treatment of bleeding episodes in individuals with inherited and acquired bleeding disorders. Transfusion Med Rev 1993; 7: 78-83.
-
(1993)
Transfusion Med Rev
, vol.7
, pp. 78-83
-
-
Hedner, U.1
Glazer, S.2
Falch, J.3
-
38
-
-
0031568684
-
Combined factors V and VIII deficiency climbs onto the map
-
Sadler J. Combined factors V and VIII deficiency climbs onto the map. J Clin Invest 1997; 99: 555-6.
-
(1997)
J Clin Invest
, vol.99
, pp. 555-556
-
-
Sadler, J.1
-
39
-
-
0001992385
-
Mutations in the gene for ERGIC-53, a protein of the endoplasmic reticulum/Golgi intermediate compartment cause combined deficiency of coagulation factors V and VIII
-
Nichols WC, Seligsohn U, Zivelin A, Terry VH, Hertel CE, Wheatley MA, Moussali MJ, Hauri HP, Ciavarella N, Kaufman RJ, Ginsburg D. Mutations in the gene for ERGIC-53, a protein of the endoplasmic reticulum/Golgi intermediate compartment cause combined deficiency of coagulation factors V and VIII. Cell 1998; 93: 61-4.
-
(1998)
Cell
, vol.93
, pp. 61-64
-
-
Nichols, W.C.1
Seligsohn, U.2
Zivelin, A.3
Terry, V.H.4
Hertel, C.E.5
Wheatley, M.A.6
Moussali, M.J.7
Hauri, H.P.8
Ciavarella, N.9
Kaufman, R.J.10
Ginsburg, D.11
-
40
-
-
0017746511
-
Immunological studies in combined factor V and factor VIII deficiency
-
Giddings JC, Seligsohn U, Bloom AL. Immunological studies in combined factor V and factor VIII deficiency. Br J Haematol 1977; 37: 257.
-
(1977)
Br J Haematol
, vol.37
, pp. 257
-
-
Giddings, J.C.1
Seligsohn, U.2
Bloom, A.L.3
-
41
-
-
0019805540
-
Familial multiple coagulation factor deficiency
-
Soff GA, Levin J. Familial multiple coagulation factor deficiency. Sem Thromb Haemostas 1981; 7: 112-48.
-
(1981)
Sem Thromb Haemostas
, vol.7
, pp. 112-148
-
-
Soff, G.A.1
Levin, J.2
-
42
-
-
0031881892
-
Bleeding symptoms in 27 Iranian patients with factor V and VIII combined deficiency
-
Peyvandi F, Tuddenham EGD, Akhtari M, Lak M, Mannucci PM. Bleeding symptoms in 27 Iranian patients with factor V and VIII combined deficiency. Br J Haematol 1998; 100: 773-6.
-
(1998)
Br J Haematol
, vol.100
, pp. 773-776
-
-
Peyvandi, F.1
Tuddenham, E.G.D.2
Akhtari, M.3
Lak, M.4
Mannucci, P.M.5
-
43
-
-
0020322169
-
Combined factor V and factor VIII deficiency among non-Ashkenazi Jews
-
Seligsohn U, Zivelin A, Zweang E. Combined factor V and factor VIII deficiency among non-Ashkenazi Jews. New Engl J Med 1982; 307: 1191-3.
-
(1982)
New Engl J Med
, vol.307
, pp. 1191-1193
-
-
Seligsohn, U.1
Zivelin, A.2
Zweang, E.3
-
44
-
-
0030869473
-
Factor X and its deficiency states
-
Perry DJ. Factor X and its deficiency states. Haemophilia 1997; 3: 159-72.
-
(1997)
Haemophilia
, vol.3
, pp. 159-172
-
-
Perry, D.J.1
-
45
-
-
0030804838
-
Inherited factor X deficiency: Molecular genetics and pathophysiology
-
Cooper DN, Millar DS, Wacey A, Pemberton S, Tuddenham EGD. 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.D.5
-
46
-
-
0000083752
-
Generation and characterization of factor X deficient mice
-
Rosen ED, Liang Z, Cooper A, Dewerchin M. Carmeliet P, Collen D, Castellino FJ. Generation and characterization of factor X deficient mice. Blood 1998; 92 (Suppl. 1), 473a.
-
(1998)
Blood
, vol.92
, Issue.SUPPL. 1
-
-
Rosen, E.D.1
Liang, Z.2
Cooper, A.3
Dewerchin, M.4
Carmeliet, P.5
Collen, D.6
Castellino, F.J.7
-
47
-
-
0031848372
-
Congenital factor X deficiency: Spectrum of bleeding symptoms in 32 Iranian patients
-
Peyvandi F, Mannucci PM, Lak M, Abdoullahi M, Zeináli S, Sharifian R, Perry DJ. Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients. Br J Haematol 1998; 102: 626-8.
-
(1998)
Br J Haematol
, vol.102
, pp. 626-628
-
-
Peyvandi, F.1
Mannucci, P.M.2
Lak, M.3
Abdoullahi, M.4
Zeináli, S.5
Sharifian, R.6
Perry, D.J.7
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