Zivelin A - Search Results

1

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. Blood. 1999 Aug 1;94(3):895-901. Blood. 1999. PMID: 10419879 Free article.

2

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: zivelin a. Blood. 1996 Aug 1;88(3):877-80. Blood. 1996. PMID: 8704244 Free article.

3

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. Blood. 1997 Jan 15;89(2):397-402. Blood. 1997. PMID: 9002940 Free article.

4

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: zivelin a. 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.

5

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.

Rosenberg N, Yatuv R, Sobolev V, Peretz H, Zivelin A, Seligsohn U. Rosenberg N, et al. Among authors: zivelin a. Blood. 2003 Jun 15;101(12):4808-15. doi: 10.1182/blood-2002-08-2452. Epub 2003 Feb 27. Blood. 2003. PMID: 12609844 Free article.

6

Induction of an inhibitor antibody to factor XI in a patient with severe inherited factor XI deficiency by Rh immune globulin.

Zucker M, Zivelin A, Teitel J, Seligsohn U. Zucker M, et al. Among authors: zivelin a. Blood. 2008 Feb 1;111(3):1306-8. doi: 10.1182/blood-2007-08-108449. Epub 2007 Nov 20. Blood. 2008. PMID: 18029554 Free article.

7

[Resistance to activated protein C--a novel cause of thrombophilia].

Cycowitz Z, Seligsohn U, Zivelin A, Eldor A. Cycowitz Z, et al. Among authors: zivelin a. Harefuah. 1995 Jul;129(1-2):1-5, 80. Harefuah. 1995. PMID: 7557699 Hebrew.

8

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: zivelin a. Blood. 1995 Jan 15;85(2):429-32. Blood. 1995. PMID: 7811996 Free article.

9

Acquired von Willebrand disease in a patient with angiodysplasia resulting from immune-mediated clearance of von Willebrand factor.

Inbal A, Bank I, Zivelin A, Varon D, Dardik R, Shapiro R, Rosenthal E, Shenkman B, Gitel S, Seligsohn U. Inbal A, et al. Among authors: zivelin a. Br J Haematol. 1997 Jan;96(1):179-82. doi: 10.1046/j.1365-2141.1997.d01-1987.x. Br J Haematol. 1997. PMID: 9012706 Free article.

10

Glanzmann thrombasthenia caused by an 11.2-kb deletion in the glycoprotein IIIa (beta3) is a second mutation in Iraqi Jews that stemmed from a distinct founder.

Rosenberg N, Yatuv R, Orion Y, Zivelin A, Dardik R, Peretz H, Seligsohn U. Rosenberg N, et al. Among authors: zivelin a. Blood. 1997 May 15;89(10):3654-62. Blood. 1997. PMID: 9160670 Free article.

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