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Flow cytometric determination of percentage of red blood cell vesicles in beta - thalassemia / Christine Talaat Riad Ghobrial ; supervised Laila Abd El Rahman Hegazy , Sahar Kamal ElDin Hussein , Azza Ahmed Ali Hassan

By: Contributor(s): Language: Eng Publication details: Cairo : Christine Talaat Riad Ghobrial , 2006Description: 155P : diagrs ; 25cmOther title:
  • تقييم نسبة حويصلات كرات الدم الحمراء بجهاز التدفق الخلوى فى مرضى انيميا البحر المتوسط [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty Of Medicine - Department Of Clinical and Chemical Pathology Summary: Thalassemia is a hereditary hemolytic anemia caused by mutations in the globin gene complexCirculatory disturbances , including arterial and venous thrombosis , have been observed in these patientsAggregability of abnormal RBC and the high level of membrane - derived microparticles , stemming from activated platelets and other blood cells , have been shown to enhance procoagulant activityIt is also thought that RBC membrane - derived vesicles contribute to defects in coagulationThe present work aimed to determine the percentage of RBCs vesicles in the peripheral blood of ? - thalassemic patients , using flow cytometry , and study its relationship to the degree of severity of anaemia
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Item type Current library Home library Call number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2006.Ch.F. (Browse shelf(Opens below)) Not for loan 01010110045413000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2006.Ch.F. (Browse shelf(Opens below)) Not for loan 01020110045413000

Thesis (M.Sc.) - Cairo University - Faculty Of Medicine - Department Of Clinical and Chemical Pathology

Thalassemia is a hereditary hemolytic anemia caused by mutations in the globin gene complexCirculatory disturbances , including arterial and venous thrombosis , have been observed in these patientsAggregability of abnormal RBC and the high level of membrane - derived microparticles , stemming from activated platelets and other blood cells , have been shown to enhance procoagulant activityIt is also thought that RBC membrane - derived vesicles contribute to defects in coagulationThe present work aimed to determine the percentage of RBCs vesicles in the peripheral blood of ? - thalassemic patients , using flow cytometry , and study its relationship to the degree of severity of anaemia

Issued also as CD

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