Salomon O - Search Results

1

Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews.

Peretz H, Salomon O, Mor-Cohen R, Usher S, Zucker M, Zivelin A, Seligsohn U. Peretz H, et al. Among authors: salomon o. J Thromb Haemost. 2013 Apr;11(4):724-30. doi: 10.1111/jth.12137. J Thromb Haemost. 2013. PMID: 23332144 Free article.

2

Analysis of genetic polymorphisms related to thrombosis and other risk factors in patients with retinal vein occlusion.

Salomon O, Moisseiev J, Rosenberg N, Vidne O, Yassur I, Zivelin A, Treister G, Steinberg DM, Seligsohn U. Salomon O, et al. Blood Coagul Fibrinolysis. 1998 Oct;9(7):617-22. doi: 10.1097/00001721-199810000-00008. Blood Coagul Fibrinolysis. 1998. PMID: 9863710

3

Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment.

Salomon O, Steinberg DM, Zivelin A, Gitel S, Dardik R, Rosenberg N, Berliner S, Inbal A, Many A, Lubetsky A, Varon D, Martinowitz U, Seligsohn U. Salomon O, et al. Arterioscler Thromb Vasc Biol. 1999 Mar;19(3):511-8. doi: 10.1161/01.atv.19.3.511. Arterioscler Thromb Vasc Biol. 1999. PMID: 10073951

4

Analysis of prothrombotic and vascular risk factors in patients with nonarteritic anterior ischemic optic neuropathy.

Salomon O, Huna-Baron R, Kurtz S, Steinberg DM, Moisseiev J, Rosenberg N, Yassur I, Vidne O, Zivelin A, Gitel S, Davidson J, Ravid B, Seligsohn U. Salomon O, et al. Ophthalmology. 1999 Apr;106(4):739-42. doi: 10.1016/S0161-6420(99)90159-8. Ophthalmology. 1999. PMID: 10201595

5

Risk factors associated with postpartum ovarian vein thrombosis.

Salomon O, Apter S, Shaham D, Hiller N, Bar-Ziv J, Itzchak Y, Gitel S, Rosenberg N, Strauss S, Kaufman N, Seligsohn U. Salomon O, et al. Thromb Haemost. 1999 Sep;82(3):1015-9. Thromb Haemost. 1999. PMID: 10494756

6

Role of aspirin in reducing the frequency of second eye involvement in patients with non-arteritic anterior ischaemic optic neuropathy.

Salomon O, Huna-Baron R, Steinberg DM, Kurtz S, Seligsohn U. Salomon O, et al. Eye (Lond). 1999 Jun;13 ( Pt 3a):357-9. doi: 10.1038/eye.1999.90. Eye (Lond). 1999. PMID: 10624433

7

Homocysteine and oxidized low density lipoprotein enhanced platelet adhesion to endothelial cells under flow conditions: distinct mechanisms of thrombogenic modulation.

Dardik R, Varon D, Tamarin I, Zivelin A, Salomon O, Shenkman B, Savion N. Dardik R, et al. Among authors: salomon o. Thromb Haemost. 2000 Feb;83(2):338-44. Thromb Haemost. 2000. PMID: 10739396

8

Thrombophilia as a cause for central and branch retinal artery occlusion in patients without an apparent embolic source.

Salomon O, Huna-Baron R, Moisseiev J, Rosenberg N, Rubovitz A, Steinberg DM, Davidson J, Sela BA, Seligsohn U. Salomon O, et al. Eye (Lond). 2001 Aug;15(Pt 4):511-4. doi: 10.1038/eye.2001.164. Eye (Lond). 2001. PMID: 11767028

9

Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism.

Salomon O, Rosenberg N, Zivelin A, Steinberg DM, Kornbrot N, Dardik R, Inbal A, Seligsohn U. Salomon O, et al. Hematol J. 2001;2(1):38-41. doi: 10.1038/sj.thj.6200078. Hematol J. 2001. PMID: 11920232

10

Prevalence, causes, and characterization of factor XI inhibitors in patients with inherited factor XI deficiency.

Salomon O, Zivelin A, Livnat T, Dardik R, Loewenthal R, Avishai O, Steinberg DM, Rosove MH, O'Connell N, Lee CA, Seligsohn U. Salomon O, et al. Among authors: o connell n. Blood. 2003 Jun 15;101(12):4783-8. doi: 10.1182/blood-2002-09-2794. Epub 2003 Feb 13. Blood. 2003. PMID: 12586617 Free article.

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