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Vitamin E and selenium concentration in Egyptian chronic hemolytic anemia's : Are they deficient / Alaa Mohamed Jamal Eldeen Esmail ; Supervised Mona Mohamed Hamdy , Dalia Sayed Mosalam , Walaa Ahmed Rabie

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Alaa Mohamed Jamal Eldeen Esmail , 2014Description: 160 P. : charts , facsimiles ; 25cmOther title:
  • تركيز فيتامين هـ و عنصر السلينيوم فى الاطفال المصريين الذين يعانون من فقر الدم الانحلالى المزمن : هل هم ناقصين [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics Summary: Increased oxidative damage is well known in chronic hemoglobinopathies due to increased resting oxygen consumption and circulating pro - oxidative free hemoglobin. But it is still unknown whether the level of antioxidants like vitamin E level and selenium differ in beta thalassemia and sickle cell anemia or contribute to differences in the severity of oxidative damage in these two diseases. The present study was carried out to investigate the antioxidants (vitamin E and selenium) and lipid profile in transfusion dependant Egyptian children with beta thalassemia and sickle cell anemia and to examine whether these variables differ in these two diseases or correlate with iron overload status or transfusion requirements
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.28.M.Sc.2014.Al.V (Browse shelf(Opens below)) Not for loan 01010110064354000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.28.M.Sc.2014.Al.V (Browse shelf(Opens below)) 64354.CD Not for loan 01020110064354000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics

Increased oxidative damage is well known in chronic hemoglobinopathies due to increased resting oxygen consumption and circulating pro - oxidative free hemoglobin. But it is still unknown whether the level of antioxidants like vitamin E level and selenium differ in beta thalassemia and sickle cell anemia or contribute to differences in the severity of oxidative damage in these two diseases. The present study was carried out to investigate the antioxidants (vitamin E and selenium) and lipid profile in transfusion dependant Egyptian children with beta thalassemia and sickle cell anemia and to examine whether these variables differ in these two diseases or correlate with iron overload status or transfusion requirements

Issued also as CD

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