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The Israel Medical Association Journal : IMAJ|February 17, 2021
Pediatric Otogenic Cerebral Sinus Vein Thrombosis and ThrombophiliaKfir Siag, Salim Mazzawi, Ariel Koren, et al.The Israel Medical Association Journal : IMAJ|July 17, 2009
Sickle cell anemia in northern Israel: screening and preventionAriel Koren, Lucia Zalman, Haya Palmor, et al.Harefuah|December 13, 2002
[The prevention programs for beta thalassemia in the Jezreel and Eiron valleys: results of fifteen years experience]Ariel Koren, Lucia Zalman, Haia Palmor, et al.European Journal of Haematology|April 3, 2004
Molecular characterization of three novel Fanconi anemia mutations in Israeli ArabsHannah Tamary, Orly Dgany, Helen Toledano, et al.British Journal of Haematology|August 31, 2006
Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic seraOrly Weizer-Stern, Konstantin Adamsky, Ninette Amariglio, et al.Cells|September 28, 2023
The Impact of Ca2+ on Intracellular Distribution of Hemoglobin in Human ErythrocytesLeonid Livshits, Sari Peretz, Anna Bogdanova, et al.Thrombosis and Haemostasis|October 7, 2004
Paediatric cerebral sinus vein thrombosis. A multi-center, case-controlled studyGili Kenet, Dalia Waldman, Aharon Lubetsky, et al.Digital Health|December 6, 2024
Artificial intelligence-enabled non-invasive ubiquitous anemia screening: The HEMO-AI pilot study on pediatric populationDaniel Gordon, Jason Hoffman, Keren Gamrasni, et al.Clinical Immunology (Orlando, Fla.)|June 6, 2017
STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compoundsSchafiq Nabhani, Cyrill Schipp, Hagit Miskin, et al.Pediatric Blood & Cancer|October 7, 2014
Genetic analysis and clinical picture of severe congenital neutropenia in IsraelAsaf Lebel, Joanne Yacobovich, Tanya Krasnov, et al.Pageof 7