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Association of factor V leiden and prothrombin gene mutations with thrombotic risk in patients with sickle cell anemia / Rania Srag Eldin Sayed ; Supervised Mona Salah Eldin Hamdy , Heba Mahmoud Gouda , Iman Abdelmohsen Abdu Shaheen

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Rania Srag Eldin Sayed , 2010Description: 112P. : charts , facsimiles ; 25cmOther title:
  • العلاقة بين التحور الجينى لعامل التجلط الخامس و البروثروبين و احتمال التجلط فى مرضى الانيميا المنجلية [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: Sickle cell disease ( SCD ) is a group of genetic disorders of hemoglobin that causes multisystem morbidity and an increased risk of early death . Vascular complications are an important aspect of sick cell anemia although there is controversial evidence surrounding the role of thrombosis in the complication . Among the crucial inherited risk factors are factor V Leiden ( G1619A ) and prothrombin gene G20210A mutations
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Item type Current library Home library Call number Copy number Status Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2010.Ra.A (Browse shelf(Opens below)) Not for loan 01010110054112000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2010.Ra.A (Browse shelf(Opens below)) 54112.CD Not for loan 01020110054112000

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

Sickle cell disease ( SCD ) is a group of genetic disorders of hemoglobin that causes multisystem morbidity and an increased risk of early death . Vascular complications are an important aspect of sick cell anemia although there is controversial evidence surrounding the role of thrombosis in the complication . Among the crucial inherited risk factors are factor V Leiden ( G1619A ) and prothrombin gene G20210A mutations

Issued also as CD

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