Zobrazeno 1 - 10
of 571
pro vyhledávání: '"A. Zivelin"'
Publikováno v:
In Journal of Thrombosis and Haemostasis April 2013 11(4):724-730
Publikováno v:
In Journal of Thrombosis and Haemostasis October 2011 9(10):1977-1984
Autor:
Rubin-Asher, Deborah, Zeilig, Gabriel, Ratner, Aba, Asher, Ilan, Zivelin, Ariella, Seligsohn, Uri, Lubetsky, Aaron
Publikováno v:
In Thrombosis Research 2010 125(6):501-504
Publikováno v:
In Journal of Thrombosis and Haemostasis June 2009 7(6):970-975
Autor:
Michal Zucker, Ariella Zivelin, Meytal Landau, Ophira Salomon, Gili Kenet, Frederic Bauduer, Michel Samama, Jacqueline Conard, Marie-Hélène Denninger, Abu-Samra Hani, Micheline Berruyer, Donald Feinstein, Uri Seligsohn
Publikováno v:
Haematologica, Vol 92, Iss 10 (2007)
Background and Objectives Factor XI (FXI) deficiency is a rare autosomal recessive disorder, the main manifestation of which is injury-related bleeding. The disorder is rare in most populations, but common among Jews in whom two mutations, E117X and
Externí odkaz:
https://doaj.org/article/47f3ce0a707347499acff32ff6842104
Autor:
Bolton‐Maggs, P.H.B. *, Peretz, H., Butler, R., Mountford, R., Keeney, S., Zacharski, L., Zivelin, A., Seligsohn, U.
Publikováno v:
In Journal of Thrombosis and Haemostasis June 2004 2(6):918-924
Autor:
Rosenberg, Nurit, Yatuv, Rivka, Sobolev, Vladimir, Peretz, Hava, Zivelin, Ariella, Seligsohn, Uri *
Publikováno v:
In Blood 15 June 2003 101(12):4808-4815
Autor:
Salomon, Ophira, Zivelin, Ariella, Livnat, Tami, Dardik, Rima, Loewenthal, Ron, Avishai, Ophelia, Steinberg, David M., Rosove, Michael H., O’Connell, Niamh, Lee, Christine A., Seligsohn, Uri *
Publikováno v:
In Blood 15 June 2003 101(12):4783-4788
Autor:
Salomon, O., Steinberg, D.M., Dardik, R., Rosenberg, N., Zivelin, A., Tamarin, I., Ravid, B., Berliner, S., Seligsohn, U. *
Publikováno v:
In Journal of Thrombosis and Haemostasis April 2003 1(4):658-661
Autor:
Uri Seligsohn, Avigal Lask, Amihai Rottenstreich, Yosef Kalish, Ariella Zivelin, Lilliana Schliamser
Publikováno v:
Journal of Thrombosis and Thrombolysis. 42:261-266
Inherited afibrinogenemia and hypofibrinogenemia are rare bleeding disorders characterized by markedly reduced levels of fibrinogen in blood. Thrombotic complications in these disorders have been rarely described. We performed a multicenter retrospec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::992d3e59327913bd4eb3f23320484dc5
https://doi.org/10.1007/s11239-015-1325-0
https://doi.org/10.1007/s11239-015-1325-0