-
2
-
-
0028899613
-
One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (Type 11) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews
-
Shpilberg O, Peretz H, Zivelin A et al. One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (Type 11) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews. Blood 1995; 85: 429-32.
-
(1995)
Blood
, vol.85
, pp. 429-432
-
-
Shpilberg, O.1
Peretz, H.2
Zivelin, A.3
-
3
-
-
0019404547
-
Definition of the population at risk of bleeding due to factor XI deficiency in Ashkenazic Jews and the value of activated partial thromboplastin time in its detection
-
Seligsohn U, Modan M. Definition of the population at risk of bleeding due to factor XI deficiency in Ashkenazic Jews and the value of activated partial thromboplastin time in its detection. Isr J Med Sci 1981; 17: 413-5.
-
(1981)
Isr J Med Sci
, vol.17
, pp. 413-415
-
-
Seligsohn, U.1
Modan, M.2
-
4
-
-
67849097372
-
Factor XI deficiency in humans
-
Seligsohn U. Factor XI deficiency in humans. J Thromb Haemost 2009; 7: 84-7.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 84-87
-
-
Seligsohn, U.1
-
5
-
-
0028869947
-
Definition of the bleeding tendency in factor XI-deficient kindreds - a clinical and laboratory study
-
Bolton-Maggs PH, Patterson DA, Wensley RT, Tuddenham EG. Definition of the bleeding tendency in factor XI-deficient kindreds - a clinical and laboratory study. Thromb Haemost 1995; 73: 194-202.
-
(1995)
Thromb Haemost
, vol.73
, pp. 194-202
-
-
Bolton-Maggs, P.H.1
Patterson, D.A.2
Wensley, R.T.3
Tuddenham, E.G.4
-
6
-
-
70449381348
-
Recombinant activated factor VII and tranexamic acid are haemostatically effective during major surgery in factor XI-deficient patients with inhibitor antibodies
-
Livnat T, Tamarin I, Mor Y et al. Recombinant activated factor VII and tranexamic acid are haemostatically effective during major surgery in factor XI-deficient patients with inhibitor antibodies. Thromb Haemost 2009; 102: 487-92.
-
(2009)
Thromb Haemost
, vol.102
, pp. 487-492
-
-
Livnat, T.1
Tamarin, I.2
Mor, Y.3
-
7
-
-
47649083020
-
Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiency
-
O'Connell NM, Riddell AF, Pascoe G, Perry DJ, Lee CA. Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiency. Haemophilia 2008; 14: 775-81.
-
(2008)
Haemophilia
, vol.14
, pp. 775-781
-
-
O'Connell, N.M.1
Riddell, A.F.2
Pascoe, G.3
Perry, D.J.4
Lee, C.A.5
-
8
-
-
69949102958
-
Lower doses of rFVIIa therapy are safe and effective for surgical interventions in patients with severe FXI deficiency and inhibitors
-
Kenet G, Lubetsky A, Luboshitz J et al. Lower doses of rFVIIa therapy are safe and effective for surgical interventions in patients with severe FXI deficiency and inhibitors. Haemophilia 2009; 15: 1065-73.
-
(2009)
Haemophilia
, vol.15
, pp. 1065-1073
-
-
Kenet, G.1
Lubetsky, A.2
Luboshitz, J.3
-
10
-
-
0024473623
-
Epidural versus general anaesthesia for elective caesarean section. Effect on Apgar score and acid-base status of the newborn
-
Evans CM, Murphy JF, Gray OP, Rosen M. Epidural versus general anaesthesia for elective caesarean section. Effect on Apgar score and acid-base status of the newborn. Anaesthesia 1989; 44: 778-82.
-
(1989)
Anaesthesia
, vol.44
, pp. 778-782
-
-
Evans, C.M.1
Murphy, J.F.2
Gray, O.P.3
Rosen, M.4
-
11
-
-
0023814502
-
Epidural analgesia vs. general anesthesia for cesarean section
-
Juul J, Lie B, Friberg Nielsen S. Epidural analgesia vs. general anesthesia for cesarean section. Acta Obstet Gynecol Scand 1998; 67: 203-6.
-
(1998)
Acta Obstet Gynecol Scand
, vol.67
, pp. 203-206
-
-
Juul, J.1
Lie, B.2
Friberg Nielsen, S.3
-
13
-
-
0037349343
-
Thrombocytopenia, low molecular weight heparin, and obstetric anesthesia
-
Abramovitz S, Beilin Y. Thrombocytopenia, low molecular weight heparin, and obstetric anesthesia. Anesthesiol Clin North America 2003; 21: 99-109.
-
(2003)
Anesthesiol Clin North America
, vol.21
, pp. 99-109
-
-
Abramovitz, S.1
Beilin, Y.2
-
14
-
-
69949099121
-
Pregnancy and rare bleeding disorders
-
Kadir R, Chi C, Bolton-Maggs P. Pregnancy and rare bleeding disorders. Haemophilia 2009; 15: 990-1005.
-
(2009)
Haemophilia
, vol.15
, pp. 990-1005
-
-
Kadir, R.1
Chi, C.2
Bolton-Maggs, P.3
-
15
-
-
47649096167
-
Guideline on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders
-
Keeling D, Tait C, Makris M. Guideline on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders. Haemophilia 2008; 14: 671-84.
-
(2008)
Haemophilia
, vol.14
, pp. 671-684
-
-
Keeling, D.1
Tait, C.2
Makris, M.3
-
16
-
-
0026730803
-
Dental surgery in patients with severe factor XI deficiency without plasma replacement
-
Berliner S, Horowitz I, Martinowitz U, Brenner B, Seligsohn U. Dental surgery in patients with severe factor XI deficiency without plasma replacement. Blood Coagul Fibrinolysis 1992; 3: 465-8.
-
(1992)
Blood Coagul Fibrinolysis
, vol.3
, pp. 465-468
-
-
Berliner, S.1
Horowitz, I.2
Martinowitz, U.3
Brenner, B.4
Seligsohn, U.5
-
17
-
-
0025477245
-
Factor VIIa in the treatment of haemophilia
-
Hedner U. Factor VIIa in the treatment of haemophilia. Blood Coagul Fibrinolysis 1990; 1: 307-17.
-
(1990)
Blood Coagul Fibrinolysis
, vol.1
, pp. 307-317
-
-
Hedner, U.1
|