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THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA
George J Kontoghiorghes, Marios Kleanthous, Christina N. Kontoghiorghe
Abstract 1642 | PDF Downloads 1044 HTML Downloads 229
Page e2020011
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IRON DEFICIENCY ANAEMIA AMONG PRE-SCHOOL CHILDREN WITH SICKLE CELL ANAEMIA: STILL A RARE DIAGNOSIS?
Olufemi Samuel Akodu, Omolara Adeolu Kehinde, Ijeoma Nnena Diaku-Akinwumi, Olisamedua Fidelis Njokanma
Abstract 911 | PDF Downloads 543 HTML Downloads 2780 cover leer Downloads 0
Page e2013069
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cover leer
INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES
Bianca Maria Ricerca, Arturo Di Girolamo, Deborah Rund
Abstract 801 | PDF Downloads 441 HTML Downloads 4116
Page e2009028
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THALASSAEMIA INTERMEDIA : AN UPDATE
Ali Taher, Khaled M. Musallam, Maria Domenica Cappellini
Abstract 769 | PDF Downloads 326 HTML Downloads 9152
Page e2009004
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STUDY OF SERUM HAPTOGLOBIN LEVEL AND ITS RELATION TO ERYTHROPOIETIC ACTIVITY IN BETA THALASSEMIA CHILDREN .
Seham Ragab, Manal A. Safan, Eman A. Badr
Abstract 1670 | PDF Downloads 874 HTML Downloads 2525 Study of serum haptoglobin level in thalassemia Downloads 0 Figures Downloads 0
Page e2015019
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Study of serum haptoglobin level in thalassemia
Figures
The IMPACT OF SUPEROXIDE DISMUTASE GENETIC POLYMORPHISM (SOD2 VAL16ALA) AND SUPEROXIDE DISMUTASE LEVEL ON DISEASE SEVERITY IN A COHORT OF EGYPTIAN SICKLE CELL DISEASE PATIENTS IN EGYPT
Mervat Khorshied, Iman A, Shaheen, Yasmeen M.M Selim, Asmaa O. Elshahawy, Ilham Youssry
Abstract 462 | PDF Downloads 364 HTML Downloads 191
Page e2022037
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HEMATOPOIETIC STEM CELL TRANSPLANTATION IN THALASSEMIA AND SICKLE CELL DISEASE: EXPERIENCE OF MEDITERRANEAN INSTITUTE OF HEMATOLOGY IN A MULTI-ETHNIC POPULATION.
Marco Marziali, Antonella Isgrò, Javid Gaziev, Guido Lucarelli
Abstract 1222 | PDF Downloads 526 HTML Downloads 2827
Page e2009027
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