Eliezer A. Rachmilewitz

Author

Also Known As

E A Rachmilewitz, ELIEZER A. RACHMILEWITZ, Eliezer A Rachmilewitz, Eliezer A. Rachmilewitz, Eliezer Rachmilewitz, Galia Spectre, Mehran Karimi, Rachmilewitz, Eliezer A

231

Publications

9.9K

Citations

H-Index

138

Concepts

All Affiliations

Hadassah Medical Center Hadassah Academic College Wolfson Medical Center Hebrew University of Jerusalem Cornell University

About

Eliezer A. Rachmilewitz is an author at Hadassah Medical Center specializing in medicine, hematology, and health sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	55	2.7K
2	Health Sciences	14	15	939
3	Public Health	4	4	600
4	Natural Sciences	3	3	107
5	Education	1	1	17

Eliezer A. Rachmilewitz

102

Publications

6.2K

Citations

H-Index

Page 1

	Year	Citations
Non‐Specific Serum Iron in Thalassaemia: an Abnormal Serum Iron Fraction of Potential Toxicity Chaim Hershko, G. Graham, George W. Bates, British Journal of Haematology	1978	423
Prevalence of thromboembolic events among 8,860 patients with thalassaemia major and intermedia in the Mediterranean area and Iran Alì Taher, Hussain Isma’eel, Ghassan Mehio, Thrombosis and Haemostasis Multiple Choice QuestionnaireThrombosisVenous ThrombosisMediterranean AreaThromboembolic Events	2006	340
Ineffective erythropoiesis in β-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin Sara Gardenghi, Maria Franca Marongiu, Pedro Luiz Ramos, Blood	2007	313
Unstable β-globin mRNA in mRNA-deficient β0 thalassemia Lynne E. Maquat, Alan J. Kinniburgh, Eliezer A. Rachmilewitz, Cell GeneticsUnstable β-Globin MrnaHematologyHeme HomeostasisGene Expression	1981	274
Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice Sara Gardenghi, Pedro Luiz Ramos, Maria Franca Marongiu, Journal of Clinical Investigation Iron MetabolismExcessive Iron AbsorptionIron DeficiencyRedox BiologyOxidative Stress	2010	218
Red blood cells, platelets and polymorphonuclear neutrophils of patients with sickle cell disease exhibit oxidative stress that can be ameliorated by antioxidants Johnny Amer, Hussam Ghoti, Eliezer A. Rachmilewitz, British Journal of Haematology	2005	207
Protective effects of tea polyphenols against oxidative damage to red blood cells Leonid Grinberg, Harold L. Newmark, Nahum Kitrossky, Biochemical Pharmacology Tea PolyphenolsMedicineLipid PeroxidationToxicologyProtective Effects	1997	186
Phosphatidylserine in the outer leaflet of red blood cells from β‐thalassemia patients may explain the chronic hypercoagulable state and thrombotic episodes Vered Borenstain‐Ben Yashar, Yechezkel Barenholz, Esther Hy‐Am, American Journal of Hematology	1993	168
THE PRESENT STATUS OF THE HETEROGENEITY OF FETAL HEMOGLOBIN IN β‐THALASSEMIA: AN ATTEMPT TO UNIFY SOME OBSERVATIONS IN THALASSEMIA AND RELATED CONDITIONS* T. H. J. Huisman, W. A. Schroeder, Georgi D. Efremov, Annals of the New York Academy of Sciences ImmunohematologyPresent StatusLaboratory HematologyHeme HomeostasisHematology	1974	165
Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia I.V. Libani, Ella Guy, Luca Melchiori, Blood	2008	159

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