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International Journal of Molecular Sciences|October 29, 2025
Hemoglobin A1C: Intracellular Heterogeneity and Functional Implications in Prediabetic and T2 Diabetic ErythrocytesGalina Petukhova, Areen Wani, Gregory Barshtein, et al.
International Journal of Molecular Sciences|September 28, 2021
Extracellular Vesicle MicroRNA That Are Involved in β-Thalassemia ComplicationsCarina Levin, Ariel Koren, Annie Rebibo-Sabbah, et al.
Mediterranean Journal of Hematology and Infectious Diseases|July 22, 2022
Back to the "Gold Standard": How Precise is Hematocrit Detection Today?Leonid Livshits, Tal Bilu, Sari Peretz, et al.
Pediatric Blood & Cancer|May 8, 2013
Small-platelet thrombocytopenia in a family with autosomal recessive inheritance patternCarina Levin, Lucia Zalman, Hannah Tamary, et al.
The Israel Medical Association Journal : IMAJ|December 31, 2005
Thrombophilia: a risk factor for cerebral palsy?Vered Yehezkely-Schildkraut, Miriam Kutai, Yaser Hugeirat, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 4, 2008
Correlation of vascular endothelial growth factor with the severity of thalassemia intermediaDavid Shitrit, Hannah Tamary, Ariel Koren, et al.
Frontiers in Physiology|September 15, 2022
The protective effect of the spleen in sickle cell patients. A comparative study between patients with asplenia/hyposplenism and hypersplenismSari Peretz, Leonid Livshits, Etheresia Pretorius, et al.
European Journal of Haematology|November 1, 2015
Hb TAYBE: clinical and morphological findings IN 43 patientsAriel Koren, Carina Levin, Luci Zalman, et al.
American Journal of Hematology|January 9, 2008
Response to hydroxyurea therapy in beta-thalassemiaAriel Koren, Carina Levin, Orly Dgany, et al.
BMC Nephrology|December 21, 2021
Renal function in β-thalassemia major patients treated with two different iron-chelation regimesOsama Tanous, Yossi Azulay, Raphael Halevy, et al.
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