Detalles de la búsqueda
1.
Thromboembolic events in patients with severe inherited fibrinogen deficiency.
J Thromb Thrombolysis
; 42(2): 261-6, 2016 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-26712130
2.
[Laboratory evaluation of lupus anticoagulant in Israel].
Harefuah
; 149(5): 288-90, 336, 2010 May.
Artículo
en Hebreo
| MEDLINE | ID: mdl-20941871
3.
Characterization of seven novel mutations causing factor XI deficiency.
Haematologica
; 92(10): 1375-80, 2007 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-18024374
4.
Age estimates of ancestral mutations causing factor VII deficiency and Dubin-Johnson syndrome in Iranian and Moroccan Jews are consistent with ancient Jewish migrations.
Blood Coagul Fibrinolysis
; 18(2): 139-44, 2007 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-17287630
5.
Inhibitors to Factor XI in patients with severe Factor XI deficiency.
Semin Hematol
; 43(1 Suppl 1): S10-2, 2006 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-16427373
6.
A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients.
Hepatol Res
; 31(2): 104-11, 2005 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-15777714
7.
Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency.
Blood Coagul Fibrinolysis
; 16(1): 37-41, 2005 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-15650544
8.
Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation.
Blood Coagul Fibrinolysis
; 16(5): 369-74, 2005 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-15970722
9.
The impact of thrombin generation and rotation thromboelastometry on assessment of severity of factor XI deficiency.
Thromb Res
; 136(2): 465-73, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-26160656
10.
A mutation in LMAN1 (ERGIC-53) causing combined factor V and factor VIII deficiency is prevalent in Jews originating from the island of Djerba in Tunisia.
Blood Coagul Fibrinolysis
; 15(1): 99-102, 2004 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-15166951
11.
Effects of platelet membrane glycoprotein polymorphisms on the risk of myocardial infarction in young males.
Isr Med Assoc J
; 4(6): 411-4, 2002 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-12073410
12.
A highly sensitive thrombin generation assay for assessment of recombinant activated factor VII therapy in haemophilia patients with an inhibitor.
Thromb Haemost
; 105(4): 688-95, 2011 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-21225093
13.
Patients with severe factor XI deficiency have a reduced incidence of deep-vein thrombosis.
Thromb Haemost
; 105(2): 269-73, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-21057700
14.
Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry.
Blood Coagul Fibrinolysis
; 22(8): 673-9, 2011 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-22008904
15.
Risk factors for failure of heparin thromboprophylaxis in patients with acute traumatic spinal cord injury.
Thromb Res
; 125(6): 501-4, 2010 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-19853891
16.
Thrombin generation assay as a possible tool for assessment of reduced activity of clotting factors induced by antiphospholipid antibodies and in-vitro evaluation of treatment options.
Blood Coagul Fibrinolysis
; 20(8): 661-6, 2009 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-19730246
17.
Induction of an inhibitor antibody to factor XI in a patient with severe inherited factor XI deficiency by Rh immune globulin.
Blood
; 111(3): 1306-8, 2008 Feb 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-18029554
18.
Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24,000 years ago.
Blood
; 107(12): 4666-8, 2006 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-16493002
19.
Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene.
Blood
; 99(7): 2448-54, 2002 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-11895778
20.
Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus.
Blood
; 101(12): 4808-15, 2003 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-12609844