Seligsohn U - Search Results

1

A single genetic origin for a common Caucasian risk factor for venous thrombosis.

Zivelin A, Griffin JH, Xu X, Pabinger I, Samama M, Conard J, Brenner B, Eldor A, Seligsohn U. Zivelin A, et al. Among authors: seligsohn u. Blood. 1997 Jan 15;89(2):397-402. Blood. 1997. PMID: 9002940 Free article.

2

Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24,000 years ago.

Zivelin A, Mor-Cohen R, Kovalsky V, Kornbrot N, Conard J, Peyvandi F, Kyrle PA, Bertina R, Peyvandi F, Emmerich J, Seligsohn U. Zivelin A, et al. Among authors: seligsohn u. Blood. 2006 Jun 15;107(12):4666-8. doi: 10.1182/blood-2005-12-5158. Epub 2006 Feb 21. Blood. 2006. PMID: 16493002 Free article.

3

One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.

Shpilberg O, Peretz H, Zivelin A, Yatuv R, Chetrit A, Kulka T, Stern C, Weiss E, Seligsohn U. Shpilberg O, et al. Among authors: seligsohn u. Blood. 1995 Jan 15;85(2):429-32. Blood. 1995. PMID: 7811996 Free article.

4

Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosis.

Brenner B, Zivelin A, Lanir N, Greengard JS, Griffin JH, Seligsohn U. Brenner B, et al. Among authors: seligsohn u. Blood. 1996 Aug 1;88(3):877-80. Blood. 1996. PMID: 8704244 Free article.

5

The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin.

Peretz H, Mulai A, Usher S, Zivelin A, Segal A, Weisman Z, Mittelman M, Lupo H, Lanir N, Brenner B, Shpilberg O, Seligsohn U. Peretz H, et al. Among authors: seligsohn u. Blood. 1997 Oct 1;90(7):2654-9. Blood. 1997. PMID: 9326232 Free article.

6

A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene.

Zivelin A, Rosenberg N, Faier S, Kornbrot N, Peretz H, Mannhalter C, Horellou MH, Seligsohn U. Zivelin A, et al. Among authors: seligsohn u. Blood. 1998 Aug 15;92(4):1119-24. Blood. 1998. PMID: 9694698 Free article.

7

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. Among authors: seligsohn u. Blood Coagul Fibrinolysis. 1998 Oct;9(7):617-22. doi: 10.1097/00001721-199810000-00008. Blood Coagul Fibrinolysis. 1998. PMID: 9863710

8

Extensive venous and arterial thrombosis associated with an inhibitor to activated protein C.

Zivelin A, Gitel S, Griffin JH, Xu X, Fernandez JA, Martinowitz U, Cohen Y, Halkin H, Seligsohn U, Inbal A. Zivelin A, et al. Among authors: seligsohn u. Blood. 1999 Aug 1;94(3):895-901. Blood. 1999. PMID: 10419879 Free article.

9

The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans.

Rosenberg N, Murata M, Ikeda Y, Opare-Sem O, Zivelin A, Geffen E, Seligsohn U. Rosenberg N, et al. Among authors: seligsohn u. Am J Hum Genet. 2002 Mar;70(3):758-62. doi: 10.1086/338932. Epub 2002 Jan 4. Am J Hum Genet. 2002. PMID: 11781870 Free PMC article.

10

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene.

Zivelin A, Bauduer F, Ducout L, Peretz H, Rosenberg N, Yatuv R, Seligsohn U. Zivelin A, et al. Among authors: seligsohn u. Blood. 2002 Apr 1;99(7):2448-54. doi: 10.1182/blood.v99.7.2448. Blood. 2002. PMID: 11895778 Free article.

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