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Journal of Thrombosis and Thrombolysis|January 3, 2019
The reduced form of coagulation factor XI is associated with illness severity and coagulopathy in critically-ill septic patientsRonit Mor-Cohen, Michal Zucker, Colin Grissom, et al.
Frontiers in Public Health|April 1, 2026
Development of an evidence-based knowledge translation intervention to promote behavioral change in cerebral palsy diagnosisVivian W Y Wong, Stephanie M Glegg, Olivia Scoten, et al.
Children (Basel, Switzerland)|September 27, 2025
Investigating Pediatricians' Practice, Knowledge, and Barriers in Diagnosing Cerebral PalsyVivian Wong, Stacey D Miller, Olivia Scoten, et al.
Journal of Thrombosis and Haemostasis : JTH|December 20, 2005
A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombastheniaN Rosenberg, H Hauschner, H Peretz, et al.
Communications Medicine|November 19, 2025
Soft kidney allocation improves HLA matching and maintains allocation orderSapir Israeli, Eytan Mor, Maya Mor Cohen, et al.
Blood|February 24, 2006
Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24,000 years agoAriella Zivelin, Ronit Mor-Cohen, Victoria Kovalsky, et al.
Clinical Genetics|January 11, 2014
Founder mutation for Huntington disease in Caucasus JewsO Melamed, D M Behar, C Bram, et al.
Elife|June 23, 2018
Mechano-redox control of integrin de-adhesionFreda Passam, Joyce Chiu, Lining Ju, et al.
Internal and Emergency Medicine|August 20, 2020
Utilization of machine-learning models to accurately predict the risk for critical COVID-19Dan Assaf, Ya'ara Gutman, Yair Neuman, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 14, 2019
ONCOGENE PANEL SEQUENCING ANALYSIS IDENTIFIES CANDIDATE ACTIONABLE GENES IN ADVANCED WELL-DIFFERENTIATED GASTROENTEROPANCREATIC NEUROENDOCRINE TUMORSAmit Tirosh, J Keith Killian, Yuelin Jack Zhu, et al.
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