Zobrazeno 1 - 10
of 263
pro vyhledávání: '"Eliezer A. Rachmilewitz"'
Autor:
Eitan Fibach, Eliezer A. Rachmilewitz
Publikováno v:
F1000Research, Vol 6 (2017)
Thalassemia (thal) is an autosomal recessive, hereditary, chronic hemolytic anemia due to a partial or complete deficiency in the synthesis of α-globin chains (α-thal) or β-globin chains (β-thal) that compose the major adult hemoglobin (α2β2).
Externí odkaz:
https://doaj.org/article/407a6df142194197badc52ef559b55f0
Publikováno v:
Haematologica, Vol 98, Iss 6 (2013)
Non-transfusion-dependent thalassemias include a variety of phenotypes that, unlike patients with beta (β)-thalassemia major, do not require regular transfusion therapy for survival. The most commonly investigated forms are β-thalassemia intermedia
Externí odkaz:
https://doaj.org/article/4b7a2d3009514cc598e1aa7828f5b3e6
Publikováno v:
Critical Reviews in Oncology/Hematology. 113:156-170
Iron is an essential element for key cellular metabolic processes. However, transfusional iron overload (IOL) may result in significant cellular toxicity. IOL occurs in transfusion dependent hematologic malignancies (HM), may lead to pathological cli
Publikováno v:
Genetically Abnormal Red Cells ISBN: 9780429263989
Genetically Abnormal Red Cells
Genetically Abnormal Red Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c251bf4dea7a28cd582f749d1df988aa
https://doi.org/10.1201/9780429263989-5
https://doi.org/10.1201/9780429263989-5
Publikováno v:
Hemoglobin. 41(2)
β-Thalassemia (β-thal) is a very common disease in the Palestinian population of the Gaza Strip. We studied their mutation frequency and clinical features. Thirteen different mutations were identified. The most common mutation was IVS-I-1 (G>A) (HB
Publikováno v:
Blood. 124:873-881
Myelodysplastic syndromes (MDSs) are a group of heterogeneous clonal bone marrow disorders characterized by ineffective hematopoiesis, peripheral blood cytopenias, and potential for malignant transformation. Lower/intermediate-risk MDSs are associate
Publikováno v:
Thrombosis Research. 130:695-702
Despite remarkable advances in understanding cerebrovascular disease attributed to sickle cell anemia, data from other hemoglobinopathies have only recently started to emerge. Several brain magnetic resonance imaging studies confirm a high prevalence
Autor:
Hussam Ghoti, Eliezer A. Rachmilewitz, Orly Goitein, Eli Konen, Eitan Fibach, Ramon Simon-Lopez, Natascia Campostrini, Ze'ev Katzir, Tamar Kushnir, Raed Gaber, Domenico Girelli
Publikováno v:
European Journal of Haematology. 89:87-93
Erythropoiesis in long-term hemodialyzed (LTH) patients is supported by erythropoietin (rHuEpo) and intravenous (IV) iron. This treatment may end up in iron overload (IO) in major organs. We studied such patients for the parameters of IO in the serum
Autor:
Francesca Vinchi, Richard Sparla, Eliezer A. Rachmilewitz, Hala Zreid, Rushdy Rasras, Martina U. Muckenthaler, Gregory M. Vercellotti, John D. Belcher, Eitan Fibach, Hussam Ghoti
Publikováno v:
Atherosclerosis. 263:e107-e108
Publikováno v:
Leukemia Research. 55:S46-S47