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Acta Haematologica|October 22, 2018
A Proposed Role of Surfactant in Platelet Function and Treatment of Pulmonary Hemorrhage in Preterm and Term InfantsTal Sadeh-Vered, Nurit Rosenberg, Iris Morag, et al.
American Journal of Human Genetics|January 10, 2002
The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and AfricansNurit Rosenberg, Mitsuru Murata, Yasuo Ikeda, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 26, 2015
Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndromeHagit Hauschner, Ronit Mor-Cohen, Stefania Messineo, et al.
British Journal of Haematology|September 6, 2003
Upregulation of osteoclast alpha2beta1 integrin compensates for lack of alphavbeta3 vitronectin receptor in Iraqi-Jewish-type Glanzmann thrombastheniaMichael A Horton, Helen M Massey, Nurit Rosenberg, et al.
Cardiovascular Diabetology|June 13, 2015
High-risk type-2 diabetes mellitus patients, without prior ischemic events, have normal blood platelet functionality profiles: a cross-sectional studyGadi Shlomai, Tal Haran-Appel, Tal Sella, et al.
Journal of Women'S Health (2002)|May 27, 2005
The influence of prothrombotic polymorphisms and obstetrical and medical variables on the length of secondary postpartum hemorrhageOphira Salomon, David M Steinberg, Meirav Pshithizki, et al.
Thrombosis Research|October 31, 2015
The role of protein disulfide isomerase in the post-ligation phase of β3 integrin-dependent cell adhesionAvi Leader, Ronit Mor-Cohen, Ron Ram, et al.
Haematologica|May 10, 2007
Three novel mutations in the glycoprotein IIb gene in a patient with type II Glanzmann thrombastheniaGergely Losonczy, Nurit Rosenberg, Zoltán Boda, et al.
Harefuah|March 28, 2019
[PLATELETS FUNCTION IN A DROP OF BLOOD: FLOW CYTOMETRY ANALYSIS COMPARED TO PLATELET AGGREGATION]Hagit Hauschner, Tamar Katz, Roy Beigel, et al.
Thrombosis and Haemostasis|May 12, 2005
A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIaGergely Losonczy, Nurit Rosenberg, Csongor Kiss, et al.
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