Rachmilewitz, Eliezer A.

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice

Gardenghi, S., Ramos, P., Marongiu, M. F., Melchiori, L., Breda, L., Guy, E., Muirhead, K., Rao, N., Roy, C. N., Andrews, N. C., et al. (2010) · Journal of Clinical Investigation

Iron Metabolism and DisordersHemoglobinopathies and Related Disorders

Cited by 220

Protective effects of tea polyphenols against oxidative damage to red blood cells

Grinberg, L. N., Newmark, H., Kitrossky, N., Rahamim, E., Chevion, M., & Rachmilewitz, E. A. (1997) · Biochemical Pharmacology

Tea Polyphenols and EffectsPhytochemicals and Antioxidant Activities

Cited by 187

Phosphatidylserine in the outer leaflet of red blood cells from β‐thalassemia patients may explain the chronic hypercoagulable state and thrombotic episodes

Yashar, V. B., Barenholz, Y., Hy‐Am, E., Rachmilewitz, E. A., & Eldor, A. (1993) · American Journal of Hematology

Hemoglobinopathies and Related DisordersErythrocyte Function and Pathophysiology

Cited by 166

Decreased hepcidin mRNA expression in thalassemic mice

Adamsky, K., Weizer, O., Amariglio, N., Breda, L., Harmelin, A., Rivella, S., Rachmilewitz, E., & Rechavi, G. (2004) · British Journal of Haematology

Iron Metabolism and DisordersHemoglobinopathies and Related Disorders

Cited by 108

Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell‐line HepG2 induced by thalassaemic sera

Weizer‐Stern, O., Adamsky, K., Amariglio, N., Levin, C., Koren, A., Breuer, W., Rachmilewitz, E., Breda, L., Rivella, S., Ioav Cabantchik, Z., et al. (2006) · British Journal of Haematology

Iron Metabolism and DisordersHemoglobinopathies and Related Disorders

Cited by 80

Severe infections in thalassaemic patients: prevalence and predisposing factors

Rahav, G., Volach, V., Shapiro, M., Rund, D., Rachmilewitz, E. A., & Goldfarb, A. (2006) · British Journal of Haematology

Hemoglobinopathies and Related DisordersIron Metabolism and Disorders

Cited by 79

mRNA expression of iron regulatory genes in β-thalassemia intermedia and β-thalassemia major mouse models

Weizer-Stern, O., Adamsky, K., Amariglio, N., Rachmilewitz, E., Breda, L., Rivella, S., & Rechavi, G. (2006) · American Journal of Hematology

Iron Metabolism and DisordersHemoglobinopathies and Related Disorders

Cited by 71

The role of endocytic pathways in cellular uptake of plasma non-transferrin iron

Sohn, Y.-S., Ghoti, H., Breuer, W., Rachmilewitz, E., Attar, S., Weiss, G., & Cabantchik, Z. I. (2012) · Haematologica

Iron Metabolism and DisordersHemoglobinopathies and Related Disorders

Cited by 44

Hepcidin and Hfe in iron overload in β‐thalassemia

Gardenghi, S., Ramos, P., Follenzi, A., Rao, N., Rachmilewitz, E. A., Giardina, P. J., Grady, R. W., & Rivella, S. (2010) · Annals of the New York Academy of Sciences

Iron Metabolism and DisordersHemoglobinopathies and Related Disorders

Cited by 27