-
1
-
-
20144382370
-
Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
-
Mariani G, Herrmann F, Dolce A, Batorova A, Etro D et al. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost 2005; 93: 481-7.
-
(2005)
Thromb Haemost
, vol.93
, pp. 481-487
-
-
Mariani, G.1
Herrmann, F.2
Dolce, A.3
Batorova, A.4
Etro, D.5
-
2
-
-
0029836470
-
Immunological aspects of recombinant factor VIIa (rFVIIa) in clinical use
-
Nicolajsen EM, Hansen LL, Poulsen F, Glazer S, Hedner U. Immunological aspects of recombinant factor VIIa (rFVIIa) in clinical use. Thromb Haemost 1996; 76: 200-4.
-
(1996)
Thromb Haemost
, vol.76
, pp. 200-204
-
-
Nicolajsen, E.M.1
Hansen, L.L.2
Poulsen, F.3
Glazer, S.4
Hedner, U.5
-
3
-
-
20544448426
-
Inhibitor to factor VII in severe factor VII deficiency: Detection and course of the inhibitory response
-
Ingerslev J, Christiansen K, Sørensen B. Inhibitor to factor VII in severe factor VII deficiency: Detection and course of the inhibitory response. J Thromb Haemost 2005; 3: 799-800.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 799-800
-
-
Ingerslev, J.1
Christiansen, K.2
Sørensen, B.3
-
7
-
-
4444269047
-
Recessively inherited coagulation disorders
-
Mannucci PM, Duga S, Peyvandi F. Recessively inherited coagulation disorders. Blood 2004; 104: 1243-52.
-
(2004)
Blood
, vol.104
, pp. 1243-1252
-
-
Mannucci, P.M.1
Duga, S.2
Peyvandi, F.3
-
8
-
-
0038278822
-
Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex
-
Zhang B, Cunningham MA, Nichols WC, et al. Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex. Nat Genet. 2003; 34: 220-5.
-
(2003)
Nat Genet.
, vol.34
, pp. 220-225
-
-
Zhang, B.1
Cunningham, M.A.2
Nichols, W.C.3
-
9
-
-
1142298871
-
Medicine: K for koagulation
-
Sadler JE. Medicine: K for koagulation. Nature 2004; 427: 493-4.
-
(2004)
Nature
, vol.427
, pp. 493-494
-
-
Sadler, J.E.1
-
10
-
-
0033950264
-
Blood coagulation factor X deficiency causes partial embryonic lethality and fatal neonatal bleeding in mice
-
Dewerchin M, Liang Z, Moons L, Carmeliet P, Castellino FJ, Collen D, Rosen ED. Blood coagulation factor X deficiency causes partial embryonic lethality and fatal neonatal bleeding in mice. Thromb Haemost. 2000; 83: 185-90.
-
(2000)
Thromb Haemost.
, vol.83
, pp. 185-190
-
-
Dewerchin, M.1
Liang, Z.2
Moons, L.3
Carmeliet, P.4
Castellino, F.J.5
Collen, D.6
Rosen, E.D.7
-
11
-
-
0032560553
-
Prothrombin deficiency results in embryonic and neonatal lethality in mice
-
Sun WY, Witte DP, Degen JL, Colbert MC, Burkart MC, Holmbäck K, Xiao Q, Bugge TH, Degen SJ. Prothrombin deficiency results in embryonic and neonatal lethality in mice. Proc Natl Acad Sci USA 1998; 95: 7597-602.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 7597-7602
-
-
Sun, W.Y.1
Witte, D.P.2
Degen, J.L.3
Colbert, M.C.4
Burkart, M.C.5
Holmbäck, K.6
Xiao, Q.7
Bugge, T.H.8
Degen, S.J.9
-
12
-
-
5444227748
-
Permanent phenotypic correction of Haemophilia B in immunocompetent mice by prenatal gene therapy
-
Waddington SN, Nivsarkar M, et al. Permanent phenotypic correction of Haemophilia B in immunocompetent mice by prenatal gene therapy. Blood 2004; 104: 2714-21.
-
(2004)
Blood
, vol.104
, pp. 2714-2721
-
-
Waddington, S.N.1
Nivsarkar, M.2
-
13
-
-
0033539486
-
Short-term correction of factor VIII deficiency in a murine model of hemophilia A after delivery of adenovirus murine factor VIII in utero
-
Lipshutz GS, Sarkar R, et al. Short-term correction of factor VIII deficiency in a murine model of hemophilia A after delivery of adenovirus murine factor VIII in utero. Proc Natl Acad Sci USA 1999; 96: 13324-9.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 13324-13329
-
-
Lipshutz, G.S.1
Sarkar, R.2
-
14
-
-
85005688727
-
Results in three Australian haemophilia B patients with high-responding inhibitors treated with the Malmömodel
-
Nilsson IM, Berntorp E, Rickard KA. Results in three Australian haemophilia B patients with high-responding inhibitors treated with the Malmömodel. Haemophilia 1995; 1: 59-66.
-
(1995)
Haemophilia
, vol.1
, pp. 59-66
-
-
Nilsson, I.M.1
Berntorp, E.2
Rickard, K.A.3
-
15
-
-
6644227418
-
The MalmöInternational Brother Study (MIBS): Further support for genetic predisposition to inhibitor development in hemophilia patients
-
the MIBS Study Group
-
Astermark J, Berntorp E, White GC, Kroner BL, the MIBS Study Group. The MalmöInternational Brother Study (MIBS): Further support for genetic predisposition to inhibitor development in hemophilia patients. Haemophilia 2001; 7: 267-72.
-
(2001)
Haemophilia
, vol.7
, pp. 267-272
-
-
Astermark, J.1
Berntorp, E.2
White, G.C.3
Kroner, B.L.4
-
16
-
-
22544473061
-
Genetic defects and inhibitor development in siblings with severe hemophilia A
-
the MalmöInternational Brother Study (MIBS)
-
Astermark J, Oldenburg J, Escobar M, White GC 2nd, Berntorp E, the MalmöInternational Brother Study (MIBS). Genetic defects and inhibitor development in siblings with severe hemophilia A. Haematologica 2005; 90: 924-31.
-
(2005)
Haematologica
, vol.90
, pp. 924-931
-
-
Astermark, J.1
Oldenburg, J.2
Escobar, M.3
White II, G.C.4
Berntorp, E.5
-
17
-
-
33645751563
-
Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A
-
the MIBS Study Group
-
Astermark J, Oldenburg J, Pavlova A, Berntorp E, Lefvert AK, the MIBS Study Group. Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A. Blood 2006a; 107: 3167-72.
-
(2006)
Blood
, vol.107
, pp. 3167-3172
-
-
Astermark, J.1
Oldenburg, J.2
Pavlova, A.3
Berntorp, E.4
Lefvert, A.K.5
-
18
-
-
33845239946
-
Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A
-
Astermark J, Oldenburg J, Carlson J, Pavlova A, Kavakli K, Berntorp E, Lefvert AK. Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A. Blood 2006b; 108: 3739-45.
-
(2006)
Blood
, vol.108
, pp. 3739-3745
-
-
Astermark, J.1
Oldenburg, J.2
Carlson, J.3
Pavlova, A.4
Kavakli, K.5
Berntorp, E.6
Lefvert, A.K.7
-
19
-
-
33846420672
-
Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A
-
for the MIBS Study Group
-
Astermark J, Wang X, Oldenburg J, Berntorp E, Lefvert AK for the MIBS Study Group. Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A. J Thromb Haemost 2007; 5: 263-5.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 263-265
-
-
Astermark, J.1
Wang, X.2
Oldenburg, J.3
Berntorp, E.4
Lefvert, A.K.5
|